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Gérard Lefranc

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André Mégarbané; Alessandra Pangrazio; Sandra Sabbagh; Eliane Chouery; Gérard Lefranc; Joseph Maarawi; Anna Villa; Cristina Sobacchi
Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia.
Janet Chou; Ghassan Dbaibo; David Fraulino; Raif S Geha; Soha Ghanem; Silvia Giliani; Rima Hanna-Wakim; Adlette Inati; Jennifer Kane; Yu-Nee Lee; Gérard Lefranc; Iman Mahfouz; André Mégarbané; Luigi D Notarangelo; Irit Tirosh; Michel J Massaad
A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome.
Ramzi Lakhdar; Nadia Leban; Gérard Lefranc; Abdelhedi Miled; Jemni Ben Chibani; Sabri Denden; Asma Kassab; Jalel Knani; Amel Haj Khelil
Update in chronic obstructive pulmonary disease: role of antioxidant and metabolizing gene polymorphisms.

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All Publications

2013: André Mégarbané; Alessandra Pangrazio; Sandra Sabbagh; Eliane Chouery; Gérard Lefranc; Joseph Maarawi; Anna Villa; Cristina Sobacchi
Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia.
European journal of medical genetics 2013;56(1):32-5.
2012: Janet Chou; Ghassan Dbaibo; David Fraulino; Raif S Geha; Soha Ghanem; Silvia Giliani; Rima Hanna-Wakim; Adlette Inati; Jennifer Kane; Yu-Nee Lee; Gérard Lefranc; Iman Mahfouz; André Mégarbané; Luigi D Notarangelo; Irit Tirosh; Michel J Massaad
A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome.
The Journal of allergy and clinical immunology 2012;130(6):1414-6.
2011: Ramzi Lakhdar; Nadia Leban; Gérard Lefranc; Abdelhedi Miled; Jemni Ben Chibani; Sabri Denden; Asma Kassab; Jalel Knani; Amel Haj Khelil
Update in chronic obstructive pulmonary disease: role of antioxidant and metabolizing gene polymorphisms.
Experimental lung research 2011;37(6):364-75.
2011: Ramzi Lakhdar; Sabri Denden; Manel Haj Mouhamed; Abdelkader Chalgoum; Nadia Leban; Jalel Knani; Gérard Lefranc; Abelhadi Miled; Jemni Ben Chibani; Amel Haj Khelil
Correlation of EPHX1, GSTP1, GSTM1, and GSTT1 genetic polymorphisms with antioxidative stress markers in chronic obstructive pulmonary disease.
Experimental lung research 2011;37(4):195-204.
2011: Ramzi Lakhdar; Nadia Leban; Gérard Lefranc; Jalel Knani; Jemni Ben Chibani; HOURIA DAIMI; Sabri Denden; Mohsen Hassine; Amel Haj Khelil
Combined analysis of EPHX1, GSTP1, GSTM1 and GSTT1 gene polymorphisms in relation to chronic obstructive pulmonary disease risk and lung function impairment.
Disease markers 2011;30(5):253-63.
2011: Myrna Medlej-Hashim; Eliane Chouery; Nabiha Salem; Valérie Delague; Gérard Lefranc; Jacques Loiselet; André Mégarbané
Familial Mediterranean fever in a large Lebanese family: multiple MEFV mutations and evidence for a Founder effect of the p.[M694I] mutation.
European journal of medical genetics 2011;54(1):50-4.
2010: Ramzi Lakhdar; Sabri Denden; Jalel Knani; Nadia Leban; HOURIA DAIMI; Mohsen Hassine; Gérard Lefranc; Jemni Ben Chibani; Amel Haj Khelil
Microsomal epoxide hydrolase gene polymorphisms and susceptibility to chronic obstructive pulmonary disease in the Tunisian population.
Genetic testing and molecular biomarkers 2010;14(6):857-63.
2010: Ramzi Lakhdar; Sabri Denden; Jalel Knani; Nadia Leban; HOURIA DAIMI; Mohsen Hassine; Gérard Lefranc; Jemni Ben Chibani; Amel Haj Khelil
Association of GSTM1 and GSTT1 polymorphisms with chronic obstructive pulmonary disease in a Tunisian population.
Biochemical genetics 2010;48(7-8):647-57.
2010: Eliane Chouery; Alessandra Pangrazio; Annalisa Frattini; Anna Villa; Liesbeth Van Wesenbeeck; Elke Piters; Wim Van Hul; Fraser Coxon; Tabitha Schouten; Miep H Helfrich; Gérard Lefranc; André Mégarbané
A new familial sclerosing bone dysplasia.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2010;25(3):676-80.
2010: Sabri Denden; Amel Haj Khelil; Jalel Knani; Ramzi Lakhdar; Pascale Perrin; Gérard Lefranc; Jemni Ben Chibani
Alpha-1 antitrypsin gene polymorphism in Chronic Obstructive Pulmonary Disease (COPD).
Genetics and molecular biology 2010;33(1):23-6.
2010: R Lakhdar; S Denden; Jalel Knani; N Leban; HOURIA DAIMI; M Hassine; Gérard Lefranc; J Ben Chibani; A Haj Khelil
Relationship between glutathione S-transferase P1 polymorphisms and chronic obstructive pulmonary disease in a Tunisian population.
Genetics and molecular research : GMR 2010;9(2):897-907.
2010: Amel Haj Khelil; Sabri Denden; Nadia Leban; HOURIA DAIMI; Ramzi Lakhdhar; Gérard Lefranc; Jemni Ben Chibani; Pascale Perrin
Hemoglobinopathies in North Africa: a review.
Hemoglobin 2010;34(1):1-23.
2009: W Aouacheri; S Saka; R Djafer; Gérard Lefranc
[Protective effect of diclofenac towards the oxidative stress induced by paracetamol toxicity in rats].
Annales de biologie clinique 2009;67(6):619-27.
2009: S Denden; Wahid BRAHAM; F Amri; R Lakhdar; Gérard Lefranc; J Knani; Jemni Ben Chibani; Amel Haj Khelil
[Biochemical and molecular diagnosis of alpha 1 antitrypsin deficiency in a Tunisian family].
Annales de biologie clinique 2009;67(4):441-5.
2009: Govindan Dayanithi; Isabelle Richard; Cedric Viero; Elsa Mazuc; Sylvie Mallie; Jean Valmier; Nathalie Bourg; Muriel Herasse; Isabelle Marty; Gérard Lefranc; Paul Mangeat; Stephen Baghdiguian
Alteration of sarcoplasmic reticulum ca release in skeletal muscle from calpain 3-deficient mice.
International journal of cell biology 2009;2009():340346.
2009: Marie-Paule Lefranc; Véronique Giudicelli; Chantal Ginestoux; Joumana Jabado-Michaloud; Géraldine Folch; Fatena Bellahcene; Yan Wu; Elodie Gemrot; Xavier Brochet; Jérôme Lane; Laetitia Regnier; François Ehrenmann; Gérard Lefranc; Patrice Duroux
IMGT, the international ImMunoGeneTics information system.
Nucleic acids research 2009;37(Database issue):D1006-12.
2008: Hong Jiao; Beáta Tóth; Melinda Erdos; Ingegerd Fransson; Eva Rákóczi; Istvan Balogh; Zoltán Magyarics; Beáta Dérfalvi; Gabriella Csorba; Anna Szaflarska; Andre Megarbane; Carlo Akatcherian; Ghassan Dbaibo; Eva Rajnavölgyi; Lennart Hammarström; Juha Kere; Gérard Lefranc; László Maródi
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups.
Molecular immunology 2008;46(1):202-6.
2008: Amel Haj Khelil; S Denden; L Hlioui; NEJIB HATTAB; HOURIA DAIMI; N Leban; Pascale Perrin; Gérard Lefranc; Jemni Ben Chibani
[Alpha 1 antitrypsin polymorphism associated to asthma and emphysema in a central Tunisian population].
Annales de biologie clinique 2008;66(4):379-84.
2008: Gemma Berniell-Lee; Susana Plaza; Elena Bosch; Francesc Calafell; Eric Jourdan; Maya Césari; Gérard Lefranc; David Comas
Admixture and sexual bias in the population settlement of La Réunion Island (Indian Ocean).
American journal of physical anthropology 2008;136(1):100-7.
2008: Béatrice Benayoun; Stephen Baghdiguian; Alicia Lajmanovich; Marc Bartoli; Nathalie Daniele; Evelyne Gicquel; Nathalie Bourg; Fabrice Raynaud; Marie-Anne Pasquier; Laurence Suel; Hanns Lochmuller; Gérard Lefranc; Isabelle Richard
NF-kappaB-dependent expression of the antiapoptotic factor c-FLIP is regulated by calpain 3, the protein involved in limb-girdle muscular dystrophy type 2A.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2008;22(5):1521-9.
2008: S Denden; A Haj Khelil; P Perrin; HOURIA DAIMI; N Leban; A Ouaja; K Mahdouani; L Hlioui; Gérard Lefranc; J Ben Chibani
Alpha 1 antitrypsin polymorphism in the Tunisian population with special reference to pulmonary disease.
Pathologie-biologie 2008;56(3):106-10.
2007: Joseph Alroy; Rolf Pfannl; Angelo A Ucci; Gérard Lefranc; Annalisa Frattini; André Mégarbané
Electron microscopic findings in skin biopsies from patients with infantile osteopetrosis and neuronal storage disease.
Ultrastructural pathology 2007;31(5):333-8.
2007: N Leban; Amel Haj Khelil; HOURIA DAIMI; S Denden; F Slimene; K Mehdouani; B Abdennaji Guenounou; Gérard Lefranc; Pascale Perrin; Jemni Ben Chibani
[C3 complement polymorphism in patients suffering from obstructive chronic bronchopneumopathy in Tunisia].
Annales de biologie clinique 2007;65(3):251-6.
2007: Noëlle Souraty; Peter Noun; Claudia Djambas-Khayat; Eliane Chouery; Alessandra Pangrazio; Anna Villa; Gérard Lefranc; Annalisa Frattini; André Mégarbané
Molecular study of six families originating from the Middle-East and presenting with autosomal recessive osteopetrosis.
European journal of medical genetics 2007;50(3):188-99.
2006: Alessandra Pangrazio; Pietro Luigi Poliani; André Megarbane; Gérard Lefranc; Edoardo Lanino; Maja Di Rocco; Francesca Rucci; Franco Lucchini; Maria Ravanini; Fabio Facchetti; Mario Abinun; Paolo Vezzoni; Anna Villa; Annalisa Frattini
Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2006;21(7):1098-105.
2006: S Buhler; André Megarbane; Gérard Lefranc; Jean-Marie Tiercy; Alicia Sanchez-Mazas
HLA-C molecular characterization of a Lebanese population and genetic structure of 39 populations from Europe to India-Pakistan.
Tissue antigens 2006;68(1):44-57.
2006: Cristian Capelli; Nicola Redhead; Valentino Romano; Francesco Calì; Gérard Lefranc; Valérie Delague; André Megarbane; Alex Felice; Vincenzo L Pascali; P I Neophytou; Z Poulli; Andrea Novelletto; Patrizia Malaspina; L Terrenato; A Berebbi; M Fellous; Mark Thomas; David B Goldstein
Population structure in the Mediterranean basin: a Y chromosome perspective.
Annals of human genetics 2006;70(Pt 2):207-25.
2005: Myrna Medlej-Hashim; Jean-Louis Serre; Sandra Corbani; Odile Saab; Nadine Jalkh; Valérie Delague; Eliane Chouery; Nabiha Salem; Jacques Loiselet; Gérard Lefranc; André Mégarbané
Familial Mediterranean fever (FMF) in Lebanon and Jordan: a population genetics study and report of three novel mutations.
European journal of medical genetics 2005;48(4):412-20.
2005: Marie-Paule Lefranc; Oliver Clement; Quentin Kaas; Elodie Duprat; Patrick Chastellan; Isabelle Coelho; Kora Combres; Chantal Ginestoux; Véronique Giudicelli; Denys Chaume; Gérard Lefranc
IMGT-Choreography for immunogenetics and immunoinformatics.
In silico biology 2005;5(1):45-60.
2005: Marie-Paule Lefranc; Elodie Duprat; Quentin Kaas; Madeleine Tranne; Aude Thiriot; Gérard Lefranc
IMGT unique numbering for MHC groove G-DOMAIN and MHC superfamily (MhcSF) G-LIKE-DOMAIN.
Developmental and comparative immunology 2005;29(11):917-38.
2005: Marie-Paule Lefranc; Véronique Giudicelli; Quentin Kaas; Elodie Duprat; Joumana Jabado-Michaloud; Dominique Scaviner; Chantal Ginestoux; Oliver Clément; Denys Chaume; Gérard Lefranc
IMGT, the international ImMunoGeneTics information system.
Nucleic acids research 2005;33(Database issue):D593-7.
2005: Marie-Paule Lefranc; Christelle Pommié; Quentin Kaas; Elodie Duprat; Nathalie Bosc; Delphine Guiraudou; Christelle Jean; Manuel Ruiz; Isabelle da Piedade; Mathieu Rouard; Elodie Foulquier; Valérie Thouvenin; Gérard Lefranc
IMGT unique numbering for immunoglobulin and T cell receptor constant domains and Ig superfamily C-like domains.
Developmental and comparative immunology 2005;29(3):185-203.
2004: Myrna Medlej-Hashim; Jacques Loiselet; Gérard Lefranc; André Mégarbané
[Familial Mediterranean Fever (FMF): from diagnosis to treatment].
Santé (Montrouge, France) 2004;14(4):261-6.
2004: Myrna Medlej-Hashim; Valérie Delague; Eliane Chouery; Nabiha Salem; Mohammed Rawashdeh; Gérard Lefranc; Jacques Loiselet; André Mégarbané
Amyloidosis in familial Mediterranean fever patients: correlation with MEFV genotype and SAA1 and MICA polymorphisms effects.
BMC medical genetics 2004;5():4.
2004: Hala Mégarbané; Cynthia Zablit; Naji Waked; Gérard Lefranc; Roland Tomb; André Mégarbané
Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome: report of a new family with additional features and review.
American journal of medical genetics. Part A 2004;124A(3):323-7.
2004: Marie-Paule Lefranc; Véronique Giudicelli; Chantal Ginestoux; Nathalie Bosc; Géraldine Folch; Delphine Guiraudou; Joumana Jabado-Michaloud; Séverine Magris; Dominique Scaviner; Valérie Thouvenin; Kora Combres; David Girod; Stéphanie Jeanjean; Céline Protat; Mehdi Yousfi-Monod; Elodie Duprat; Quentin Kaas; Christelle Pommié; Denys Chaume; Gérard Lefranc
IMGT-ONTOLOGY for immunogenetics and immunoinformatics.
In silico biology 2004;4(1):17-29.
2004: Christelle Pommié; Séverine Levadoux; Robert Sabatier; Gérard Lefranc; Marie-Paule Lefranc
IMGT standardized criteria for statistical analysis of immunoglobulin V-REGION amino acid properties.
Journal of molecular recognition : JMR 2004;17(1):17-32.
2003: Susana Plaza; Francesc Calafell; Ahmed N Helal; N Bouzerna; Gérard Lefranc; Jaume Bertranpetit; David Comas
Joining the pillars of Hercules: mtDNA sequences show multidirectional gene flow in the western Mediterranean.
Annals of human genetics 2003;67(Pt 4):312-28.
2003: M Haddad; Gérard Lefranc; G Aftimos
Local application of IGF1 on dental pulp mechanically exposed; in vivo study on rabbit.
Bulletin du Groupèment international pour la recherche scientifique en stomatologie & odontologie 2003;45(1):12-7.
2003: Marie-Paule Lefranc; Christelle Pommié; Manuel Ruiz; Véronique Giudicelli; Elodie Foulquier; Lisa Truong; Valérie Thouvenin-Contet; Gérard Lefranc
IMGT unique numbering for immunoglobulin and T cell receptor variable domains and Ig superfamily V-like domains.
Developmental and comparative immunology 2003;27(1):55-77.
2002: Brian C Verrelli; John H McDonald; George Argyropoulos; Giovanni Destro-Bisol; Alain Froment; Anthi Drousiotou; Gérard Lefranc; Ahmed N Helal; Jacques Loiselet; Sarah A Tishkoff
Evidence for balancing selection from nucleotide sequence analyses of human G6PD.
American journal of human genetics 2002;71(5):1112-28.
2002: Henri de la Salle; Xavier Saulquin; Issam Mansour; Samira Klayme; Dominique Fricker; J Zimmer; Jean-Pierre Cazenave; Daniel Hanau; Marc Bonneville; Elisabeth Houssaint; Gérard Lefranc; Roger Naman
Asymptomatic deficiency in the peptide transporter associated to antigen processing (TAP).
Clinical and experimental immunology 2002;128(3):525-31.
2002: Myrna Medlej-Hashim; Nabiha Salem; Eliane Chouery; Mohammed Rawashdeh; Valérie Delague; M Haffar; Issam Mansour; Roger Naman; Gérard Lefranc; Jacques Loiselet; André Mégarbané
Familial Mediterranean fever: the potential for misdiagnosis of E148V using the E148Q usual RFLP detection method.
Clinical genetics 2002;61(1):71-3.
2001: Myrna Medlej-Hashim; Isabelle Petit; Salim M Adib; Eliane Chouery; Nabiha Salem; Valérie Delague; Mohammed Rawashdeh; Issam Mansour; Gérard Lefranc; Roger Naman; Jacques Loiselet; Jean-Claude Lecron; Jean-Louis Serre; André Mégarbané
Familial Mediterranean Fever: association of elevated IgD plasma levels with specific MEFV mutations.
European journal of human genetics : EJHG 2001;9(11):849-54.
2001: Alicia Sanchez-Mazas; E Bütler-Brunner; R Bütler; Rosario Calderón; A Chaventré; Jean-Michel Dugoujon; M Hammond; Gérard Lefranc; H Matsumoto; Ludmila P Osipova; C Politis; R Pullmann; André Langaney
A worldwide analysis of AG molecular diversity inferred from serology.
Human biology 2001;73(5):637-59.
2001: Sarah A Tishkoff; R Varkonyi; N Cahinhinan; S Abbes; George Argyropoulos; Giovanni Destro-Bisol; Anthi Drousiotou; B Dangerfield; Gérard Lefranc; Jacques Loiselet; Anna Piro; M Stoneking; Antonio Tagarelli; Giuseppe Tagarelli; Elias H Touma; scott williams; andrew clark
Haplotype diversity and linkage disequilibrium at human G6PD: recent origin of alleles that confer malarial resistance.
Science (New York, N.Y.) 2001;293(5529):455-62.
2001: Stephen Baghdiguian; Isabelle Richard; M Martin; Peter J Coopman; Jacques Beckmann; Paul Mangeat; Gérard Lefranc
Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscle.
Journal of molecular medicine (Berlin, Germany) 2001;79(5-6):254-61.
2001: Issam Mansour; Valérie Delague; Cécile Cazeneuve; Catherine Dodé; Eliane Chouery; Christophe Pêcheux; Myrna Medlej-Hashim; Nabiha Salem; L El Zein; I Levan-Petit; Gérard Lefranc; M Goossens; Marc Delpech; Serge Amselem; Jacques Loiselet; Gilles Grateau; A Mégarbane; Roger Naman
Familial Mediterranean fever in Lebanon: mutation spectrum, evidence for cases in Maronites, Greek orthodoxes, Greek catholics, Syriacs and Chiites and for an association between amyloidosis and M694V and M694I mutations.
European journal of human genetics : EJHG 2001;9(1):51-5.
2000: Isabelle Richard; Carinne Roudaut; Sylvie Marchand; Stephen Baghdiguian; M Herasse; Daniel Stockholm; Y Ono; Laurence Suel; Nathalie Bourg; Hiroyuki Sorimachi; Gérard Lefranc; M Fardeau; A Sébille; Jacques Beckmann
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice.
The Journal of cell biology 2000;151(7):1583-90.
2000: David Comas; Francesc Calafell; N Benchemsi; Ahmed N Helal; Gérard Lefranc; M Stoneking; M A Batzer; Jaume Bertranpetit; A Sajantila
Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits.
Human genetics 2000;107(4):312-9.
2000: Myrna Medlej-Hashim; Mohammed Rawashdeh; Eliane Chouery; Issam Mansour; Valérie Delague; Gérard Lefranc; Roger Naman; Jacques Loiselet; André Mégarbané
Genetic screening of fourteen mutations in Jordanian familial Mediterranean fever patients.
Human mutation 2000;15(4):384.
2000: Manuel Ruiz; Véronique Giudicelli; Chantal Ginestoux; Peter Stoehr; James Robinson; J Bodmer; Steven G E Marsh; Ronald E Bontrop; Marc Lemaitre; Gérard Lefranc; Denys Chaume; Marie-Paule Lefranc
IMGT, the international ImMunoGeneTics database.
Nucleic acids research 2000;28(1):219-21.
1999: Ludmila P Osipova; Olga L Posukh; V P Wiebe; T Miyazaki; H Matsumoto; Gérard Lefranc; Marie-Paule Lefranc
BamHI-SacI RFLP and Gm analysis of the immunoglobulin IGHG genes in the Northern Selkups (west Siberia): new haplotypes with deletion, duplication and triplication.
Human genetics 1999;105(6):530-41.
1999: Stephen Baghdiguian; M Martin; Isabelle Richard; F Pons; Catherine Astier; Nathalie Bourg; Ron Thomas Hay; Raymond Chemaly; Georges Halaby; Jacques Loiselet; Louise V B Anderson; Adolfo Lopez de Munain; M Fardeau; Paul Mangeat; Jacques Beckmann; Gérard Lefranc
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A.
Nature medicine 1999;5(5):503-11.
1998: Haifa Jabara; R H Buckley; J L Roberts; Gérard Lefranc; Jacques Loiselet; G Khalil; Raif S Geha
Role of JAK3 in CD40-mediated signaling.
Blood 1998;92(7):2435-40.
1998: F Bozzi; Gérard Lefranc; Anna Villa; Raffaele Badolato; R Fabian Schumacher; G Khalil; Jacques Loiselet; S Bresciani; John O'Shea; Paolo Vezzoni; Luigi D Notarangelo; Fabio Candotti
Molecular and biochemical characterization of JAK3 deficiency in a patient with severe combined immunodeficiency over 20 years after bone marrow transplantation: implications for treatment.
British journal of haematology 1998;102(5):1363-6.
1998: Olga L Posukh; Ludmila P Osipova; IuO Kashinskaia; Evgueni Ivakine; IuA Kriukov; Tatiana M Karafet; MA Kazakovtseva; L M Skobel'tsina; M G Crawford; Gérard Lefranc
[Genetic analysis of the South Altaian population of the Mendur-Sokkon village, Altai Republic].
Genetika 1998;34(1):106-13.
1997: Isabelle Richard; L Brenguier; Pervin Dinçer; Carinne Roudaut; B Bady; Jean-Marc Burgunder; Raymond Chemaly; C A Garcia; Georges Halaby; CE Jackson; D M Kurnit; Gérard Lefranc; C Legum; Jacques Loiselet; Luciano Merlini; A Nivelon-Chevallier; E Ollagnon-Roman; G Restagno; Haluk Topaloglu; Jacques Beckmann
Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins.
American journal of human genetics 1997;60(5):1128-38.
1997: P Dard; S Huck; JP Frippiat; Gérard Lefranc; André Langaney; Marie-Paule Lefranc; Alicia Sanchez-Mazas
The IGHG3 gene shows a structural polymorphism characterized by different hinge lengths: sequence of a new 2-exon hinge gene.
Human genetics 1997;99(1):138-41.
1996: Jacques Beckmann; Isabelle Richard; O Broux; Françoise Fougerousse; V Allamand; N Chiannilkulchai; LE Lim; F Duclos; Nathalie Bourg; L Brenguier; P Pasturaud; F Quétier; Carinne Roudaut; Y Sunada; J Meyer; Pervin Dinçer; Gérard Lefranc; Luciano Merlini; Haluk Topaloglu; Fernando M S Tomé; D Cohen; CE Jackson; Kevin P Campbell; M Fardeau
Identification of muscle-specific calpain and beta-sarcoglycan genes in progressive autosomal recessive muscular dystrophies.
Neuromuscular disorders : NMD 1996;6(6):455-62.
1996: Per-Erik Engström; G Norhagen; L Osipova; A Helal; V Wiebe; Alfredo Brusco; A O Carbonara; Gérard Lefranc; Marie-Paule Lefranc
Salivary IgG subclasses in individuals with and without homozygous IGHG gene deletions.
Immunology 1996;89(2):178-82.
1996: P Dard; Alicia Sanchez-Mazas; J M Dugoujon; G De Lange; André Langaney; Marie-Paule Lefranc; Gérard Lefranc
DNA analysis of the immunoglobulin IGHG loci in a Mandenka population from eastern Senegal: correlation with Gm haplotypes and hypotheses for the evolution of the Ig CH region.
Human genetics 1996;98(1):36-47.
1995: X M Zhang; S Huck; P Dariavach; R Spilliaert; A Arnason; Z Soua; Gérard Lefranc; Marie-Paule Lefranc
Isolation of T cell receptor gamma/delta chain constant genes from minke whale.
Experimental and clinical immunogenetics 1995;12(4):245-52.
1995: Z Soua; A Khelif; S Ennabli; M Jemmali; J Taib; Gérard Lefranc; Marie-Paule Lefranc
First study of immunoglobulin and T cell receptor gene rearrangements in chronic and acute lymphoblastic leukemias from Tunisia.
Experimental and clinical immunogenetics 1995;12(1):16-30.
1994: V Wiebe; A Helal; Marie-Paule Lefranc; Gérard Lefranc
Molecular analysis of the T17 immunoglobulin CH multigene deletion (del A1-GP-G2-G4-E).
Human genetics 1994;93(5):520-8.
1993: P Chuchana; JP Frippiat; Antoine BLANCHER; Gérard Lefranc; Marie-Paule Lefranc
Haplotypes of the human immunoglobulin lambda IGLV7S1 and IGLV1S1 genes defined by restriction-site polymorphism and insertion/deletion of a 6-kb DNA fragment.
American journal of human genetics 1993;53(2):518-25.
1992: Marie-Paule Lefranc; Gérard Lefranc
The constant region genes of the immunoglobulin heavy chains.
Advances in nephrology from the Necker Hospital 1992;21():3-12.
1992: M Weill; X M Zhang; F Bernard; Gérard Lefranc; Marie-Paule Lefranc
A rare genetic variant of the T cell receptor gamma joining segment TRGJI.
Human genetics 1992;88(3):355.
1991: Bernard Lenormand; N Ghanem; Hervé Tilly; C Boussemart; Mathieu Monconduit; H Piguet; Gérard Lefranc; Marie-Paule Lefranc
Rearrangements of immunoglobulin light and heavy chain genes and correlation with phenotypic markers in B-cell chronic lymphocytic leukemia.
Leukemia 1991;5(11):928-36.
1991: D Alexandre; P Chuchana; M G Roncarolo; H Yssel; H Spits; Gérard Lefranc; Marie-Paule Lefranc
Reciprocal hybrid joints demonstrate successive V-J rearrangements on the same chromosome in the human TCR gamma locus.
International immunology 1991;3(10):973-82.
1991: M Bensmana; F Bernard; X M Zhang; P Chuchana; Marie-Paule Lefranc; Gérard Lefranc
RFLP detected by the transmembrane exon probe of the human immunoglobulin IGHA genes.
Nucleic acids research 1991;19(18):5098.
1991: P Chuchana; D Alexandre; Gérard Lefranc; Marie-Paule Lefranc
The IGLVA gene as a STS in the human immunoglobulin lambda light chain variable gene locus (located at 22q11)
Nucleic acids research 1991;19(17):4786.
1991: M S Hassan; Manuchehr Abedi-Valugerdi; Gérard Lefranc; L Hammarström; C I Smith
Biological half-life of normal and truncated human IgG3 in scid mice.
European journal of immunology 1991;21(5):1319-22.
1991: F Bernard; F Ducret; C Buresi; Gérard Lefranc; Marie-Paule Lefranc
HindIII/EcoRI RFLP of the human immunoglobulin IGHE gene detected with a C epsilon probe in the French and Tunisian populations.
Human genetics 1991;87(1):101.
1991: N Ghanem; Z Soua; X G Zhang; M Zijun; Y Zhiwei; Gérard Lefranc; Marie-Paule Lefranc
Polymorphism of the T-cell receptor gamma variable and constant region genes in a Chinese population.
Human genetics 1991;86(5):450-6.
1991: P Chuchana; F Bernard; Gérard Lefranc; Marie-Paule Lefranc
An STS in the human T-cell receptor delta locus located at 14q11.
Nucleic acids research 1991;19(2):410.
1991: Marie-Paule Lefranc; L Hammarström; C I Smith; Gérard Lefranc
Gene deletions in the human immunoglobulin heavy chain constant region locus: molecular and immunological analysis.
Immunodeficiency reviews 1991;2(4):265-81.
1991: M Bensmana; P Chuchana; Gérard Lefranc; Marie-Paule Lefranc
Sequence of the CH1 and hinge-CH2 exons of the human immunoglobulin IGHA2 A2m(2) allele: comparison with the nonallelic and allelic IGHA genes.
Cytogenetics and cell genetics 1991;56(2):128.
1991: M Ben Salem; N Ghanem; T Kneissi; M Abbal; J M Dugoujon; J Ben Chibani; F Ellouze; Gérard Lefranc
[Immunogenetic markers (BF, C2, C4, 21-OH, TNF alpha, TCR beta, Ig) and insulin-dependent diabetes in the Tunisian population: serological and molecular study].
Annales de biologie clinique 1991;49(7):389-96.
1990: JP Frippiat; P Chuchana; F Bernard; L Buluwela; Gérard Lefranc; Marie-Paule Lefranc
First genomic sequence of a human Ig variable lambda gene belonging to subgroup III.
Nucleic acids research 1990;18(23):7134.
1990: D Alexandre; F Bernard; C Buresi; Gérard Lefranc; Marie-Paule Lefranc
A SacI RFLP of the human T-cell receptor delta (TCRD) joining segment J2.
Nucleic acids research 1990;18(23):7195.
1990: N Ghanem; Jean-Marc Lobaccaro; C Buresi; M Abbal; Georges Halaby; C Sultan; Gérard Lefranc
Defective, deleted or converted CYP21B gene and negative association with a rare restriction fragment length polymorphism allele of the factor B gene in congenital adrenal hyperplasia.
Human genetics 1990;86(2):117-25.
1990: F Bernard; P Chuchana; Gérard Lefranc; Marie-Paule Lefranc
An STS in the human T cell receptor gamma locus (located at 7p14-15).
Nucleic acids research 1990;18(20):6170.
1990: P Chuchana; Antoine BLANCHER; Gérard Lefranc; Marie-Paule Lefranc
HindIII RFLP of the human immunoglobulin V lambda III subgroup genes.
Nucleic acids research 1990;18(20):6179.
1990: Antoine BLANCHER; P Chuchana; Gérard Lefranc; Marie-Paule Lefranc
HindIII restriction fragment alleles of the human immunoglobulin V lambda II subgroup genes.
Nucleic acids research 1990;18(20):6178.
1990: G Keyeux; S Gilgenkrantz; Gérard Lefranc; Marie-Paule Lefranc
Distal trisomy 14q. II. Molecular study of the 14q32 locus in two cases of chromosome 14 rearrangements with partial duplication.
Human genetics 1990;85(6):617-22.
1990: Gérard Lefranc; Marie-Paule Lefranc
Antibody engineering and perspectives in therapy.
Biochimie 1990;72(9):639-51.
1990: Per-Erik Engström; G Norhagen; A Bottaro; A O Carbonara; Gérard Lefranc; M Steinitz; P O Söder; C I Edvard Smith; Lennart Hammarström
Subclass distribution of antigen-specific IgA antibodies in normal donors and individuals with homozygous C alpha 1 or C alpha 2 gene deletions.
Journal of immunology (Baltimore, Md. : 1950) 1990;145(1):109-16.
1990: P Chuchana; Antoine BLANCHER; F Brockly; D Alexandre; Gérard Lefranc; Marie-Paule Lefranc
Definition of the human immunoglobulin variable lambda (IGLV) gene subgroups.
European journal of immunology 1990;20(6):1317-25.
1990: Gérard Lefranc; Marie-Paule Lefranc
Regulation of the immunoglobulin gene transcription.
Biochimie 1990;72(1):7-17.
1990: Jean-Marc Lobaccaro; N Ghanem; Gérard Lefranc; C Sultan
CYP21B gene conversion and complete CYP21A gene deletion in congenital adrenal hyperplasia.
Annales de génétique 1990;33(2):70-5.
1990: G Keyeux; Marie-Paule Lefranc; Alain Chevailler; Gérard Lefranc
Molecular analysis of the IGHA and MHC class III region genes in one family with IgA and C4 deficiencies.
Experimental and clinical immunogenetics 1990;7(3):170-80.
1990: Lennart Hammarström; N Ghanem; C I Edvard Smith; Gérard Lefranc; Marie-Paule Lefranc
RFLP of human immunoglobulin genes.
Experimental and clinical immunogenetics 1990;7(1):7-19.
1990: Jean-Marc Lobaccaro; N Ghanem; Gérard Lefranc; Charles Sultan
[Molecular genetics of 21-hydroxylase deficiency in congenital adrenal hyperplasia].
Comptes rendus des séances de la Société de biologie et de ses filiales 1990;184(1):75-86.
1989: G Keyeux; Gérard Lefranc; Marie-Paule Lefranc
A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombination.
Genomics 1989;5(3):431-41.
1989: N Ghanem; M Bensmana; J M Dugoujon; J Constans; Marie-Paule Lefranc; Gérard Lefranc
BamHI and SacI RFLPs of the human immunoglobulin IGHG genes with reference to the Gm polymorphism in African people. Evidence for a major polymorphism.
Human genetics 1989;83(1):37-44.
1989: G Keyeux; S Gilgenkrantz; Gérard Lefranc; Marie-Paule Lefranc
Molecular characterization of a ring chromosome 14 showing that the PI locus is centromeric to the D14S1 and IGH loci.
Human genetics 1989;82(3):219-22.
1989: Marie-Paule Lefranc; P Chuchana; P Dariavach; C Nguyen; S Huck; F Brockly; B Jordan; Gérard Lefranc
Molecular mapping of the human T cell receptor gamma (TRG) genes and linkage of the variable and constant regions.
European journal of immunology 1989;19(6):989-94.
1989: F Brockly; D Alexandre; P Chuchana; S Huck; Gérard Lefranc; Marie-Paule Lefranc
First nucleotide sequence of a human immunoglobulin variable lambda gene belonging to subgroup II.
Nucleic acids research 1989;17(10):3976.
1989: D Alexandre; P Chuchana; F Brockly; Antoine BLANCHER; Gérard Lefranc; Marie-Paule Lefranc
First genomic sequence of a human Ig variable lambda gene belonging to subgroup I. Functional genes, pseudogenes and vestigial sequences are interspersed in the IGLV locus.
Nucleic acids research 1989;17(10):3975.
1989: Z Soua; N Ghanem; M Ben Salem; Gérard Lefranc; Marie-Paule Lefranc
Frequencies of the human immunoglobulin IGHA2*M1 and IGHA2*M2 alleles corresponding to the A2m(1) and A2m(2) allotypes in the French, Lebanese, Tunisian and black African populations.
Nucleic acids research 1989;17(9):3625.
1989: G Keyeux; Gérard Lefranc; Marie-Paule Lefranc
A specific switch alpha probe of the human immunoglobulin IGHA locus.
Nucleic acids research 1989;17(9):3624.
1989: G Keyeux; N Ghanem; Gérard Lefranc; Marie-Paule Lefranc
Identification of the PvuII RFLPs from the switch human immunoglobulin alpha (IGSA) regions.
Nucleic acids research 1989;17(9):3623.
1989: P Chuchana; Z Soua; F Brockly; X G Zhang; N Ghanem; Gérard Lefranc; Marie-Paule Lefranc
BamH I restriction fragment alleles of the human T-cell receptor delta (TRD) variable region V2.
Nucleic acids research 1989;17(9):3622.
1989: P Chuchana; Z Soua; N Ghanem; F Brockly; Gérard Lefranc; Marie-Paule Lefranc
Two KpnI restriction fragment alleles of the human T-cell receptor delta (TRD) joining segment J2.
Nucleic acids research 1989;17(3):1275.
1989: N Ghanem; P Chuchana; P Dariavach; F Brockly; Gérard Lefranc; Marie-Paule Lefranc
SacI polymorphism defined by human T-cell receptor gamma (TCRG) variable gene V11.
Nucleic acids research 1989;17(3):1271.
1989: N Ghanem; P Dariavach; Gérard Lefranc; Marie-Paule Lefranc
A TaqI RFLP of the human T-cell receptor gamma (TCRG) variable gene V11.
Nucleic acids research 1989;17(3):1270.
1989: N Ghanem; C Buresi; Gérard Lefranc; Marie-Paule Lefranc
A unique RFLP in the human T-cell receptor gamma constant region gene TRGC1.
Nucleic acids research 1989;17(1):471.
1989: Lennart Hammarström; J M Dugoujon; G G de Lange; N Ghanem; Gérard Lefranc; C I Edvard Smith
No influence of conversions affecting allotype expression on the IgG subclass restriction of specific antibodies.
Experimental and clinical immunogenetics 1989;6(1):60-7.
1989: N Ghanem; J M Dugoujon; Marie-Paule Lefranc; Gérard Lefranc
BstEII restriction fragment alleles and haplotypes of the human IGHG genes with reference to the BamHI/SacI RFLPs and to the Gm polymorphism.
Experimental and clinical immunogenetics 1989;6(1):39-54.
1989: N Ghanem; C Buresi; Jean-Paul Moisan; M Bensmana; P Chuchana; S Huck; Gérard Lefranc; Marie-Paule Lefranc
Deletion, insertion, and restriction site polymorphism of the T-cell receptor gamma variable locus in French, Lebanese, Tunisian, and black African populations.
Immunogenetics 1989;30(5):350-60.
1989: S Huck; Gérard Lefranc; Marie-Paule Lefranc
A human immunoglobulin IGHG3 allele (Gmb0,b1,c3,c5,u) with an IGHG4 converted region and three hinge exons.
Immunogenetics 1989;30(4):250-7.
1989: C Buresi; N Ghanem; S Huck; Gérard Lefranc; Marie-Paule Lefranc
Exon duplication and triplication in the human T-cell receptor gamma constant region genes and RFLP in French, Lebanese, Tunisian, and black African populations.
Immunogenetics 1989;29(3):161-72.
1988: Jean-Marc Lobaccaro; N Ghanem; C Sultan; Gérard Lefranc
A new TaqI polymorphism of the complement factor B gene.
Nucleic acids research 1988;16(24):11851.
1988: N Ghanem; B Uring-Lambert; M Abbal; georges hauptmann; Marie-Paule Lefranc; Gérard Lefranc
Polymorphism of MHC class III genes: definition of restriction fragment linkage groups and evidence for frequent deletions and duplications.
Human genetics 1988;79(3):209-18.
1988: N Ghanem; J M Dugoujon; M Bensmana; S Huck; Marie-Paule Lefranc; Gérard Lefranc
Restriction fragment haplotypes in the human immunoglobulin IGHG locus and their correlation with the Gm polymorphism.
European journal of immunology 1988;18(7):1067-72.
1988: N Ghanem; Marie-Paule Lefranc; Gérard Lefranc
Definition of the RFLP alleles in the human immunoglobulin IGHG gene locus.
European journal of immunology 1988;18(7):1059-65.
1988: Mats A A Persson; S E Brown; M W Steward; Lennart Hammarström; C I Edvard Smith; C R Howard; M Wahl; B Rynnel-Dagöö; Gérard Lefranc; A O Carbonara
IgG subclass-associated affinity differences of specific antibodies in humans.
Journal of immunology (Baltimore, Md. : 1950) 1988;140(11):3875-9.
1988: M Bensmana; S Huck; Gérard Lefranc; Marie-Paule Lefranc
The human immunoglobulin pseudo-gamma IGHGP gene shows no major structural defect.
Nucleic acids research 1988;16(7):3108.
1988: A N Helal; G de Lange; E Van Loghem; Gérard Lefranc
Uncommon Gm* haplotypes in the Tunisian population: further contribution to the genetics of the IgG immunoglobulins.
Experimental and clinical immunogenetics 1988;5(1):24-38.
1988: A N Helal; L Rivat-Peran; E Van Loghem; G de Lange; André Langaney; Gérard Lefranc
Further contribution of common Gm*-Am* haplotypes and Km* alleles in the characterization of the Tunisian population.
Experimental and clinical immunogenetics 1988;5(1):1-14.
1988: N Ghanem; P Dariavach; M Bensmana; J Chibani; Gérard Lefranc; Marie-Paule Lefranc
Polymorphism of immunoglobulin lambda constant region genes in populations from France, Lebanon and Tunisia.
Experimental and clinical immunogenetics 1988;5(4):186-95.
1987: P Dariavach; Gérard Lefranc; Marie-Paule Lefranc
Human immunoglobulin C lambda 6 gene encodes the Kern+Oz-lambda chain and C lambda 4 and C lambda 5 are pseudogenes.
Proceedings of the National Academy of Sciences of the United States of America 1987;84(24):9074-8.
1987: Lennart Hammarström; A O Carbonara; Mario DeMarchi; Gérard Lefranc; Göran Möller; C I Edvard Smith; B J Zegers
Subclass restriction pattern of antigen-specific antibodies in donors with defective expression of IgG or IgA subclass heavy chain constant region genes.
Clinical immunology and immunopathology 1987;45(3):461-70.
1987: Marie-Paule Lefranc; Gérard Lefranc
Human immunoglobulin heavy-chain multigene deletions in healthy individuals.
FEBS letters 1987;213(2):231-7.
1987: L Hammarström; A O Carbonara; Mario DeMarchi; Gérard Lefranc; Marie-Paule Lefranc; C I Smith
Generation of the antibody repertoire in individuals with multiple immunoglobulin heavy chain constant region gene deletions.
Scandinavian journal of immunology 1987;25(2):189-94.
1987: N Ghanem; Marie-Paule Lefranc; Gérard Lefranc
Polymorphism of the complement C3 gene in the Lebanese population.
Experimental and clinical immunogenetics 1987;4(4):222-6.
1986: S Huck; G Keyeux; N Ghanem; Marie-Paule Lefranc; Gérard Lefranc
A gamma 3 hinge region probe: first specific human immunoglobulin subclass probe.
FEBS letters 1986;208(2):221-30.
1986: S Huck; Philippe FORT; D H Crawford; M P Lefranc; Gérard Lefranc
Sequence of a human immunoglobulin gamma 3 heavy chain constant region gene: comparison with the other human C gamma genes.
Nucleic acids research 1986;14(4):1779-89.
1986: M P Lefranc; A N Helal; G de Lange; H Chaabani; E van Loghem; Gérard Lefranc
Gene conversion in human immunoglobulin gamma locus shown by unusual location of IgG allotypes.
FEBS letters 1986;196(1):96-102.
1986: L Hammarström; Gérard Lefranc; M P Lefranc; M A Persson; C I Smith
Aberrant pattern of anti-carbohydrate antibodies in immunoglobulin class or subclass-deficient donors.
Monographs in allergy 1986;20():50-6.
1985: J Chibani; Gérard Lefranc; J Constans
Serum protein polymorphism among Tunisian Berbers: haptoglobin, transferrin and group-specific component subtypes, C3 and BF types.
Annals of human biology 1985;12(5):449-62.
1984: Christian Davrinche; R Charlionet; C Rivat; A N Helal; Gérard Lefranc
Inulin-induced activation of factor B in whole serum: description of structural modifications in the Ba fragment.
European journal of immunology 1984;14(10):957-61.
1984: H Chaabani; A N Helal; E van Loghem; André Langaney; A Benammar Elgaaied; L Rivat Peran; Gérard Lefranc
Genetic study of Tunisian Berbers. I. Gm, Am and Km immunoglobulin allotypes and ABO blood groups.
Journal of immunogenetics 1984;11(2):107-13.
1984: H Chaabani; J P Martin; R R Frants; Gérard Lefranc
Genetic study of Tunisian Berbers. II. Alpha 1-antitrypsin (Pi) polymorphism: report of a new allele (Pi S Berber).
Experimental and clinical immunogenetics 1984;1(1):19-24.
1983: M P Lefranc; Gérard Lefranc; G de Lange; T A Out; P J van den Broek; J van Nieuwkoop; J Radl; A N Helal; H Chaabani; E van Loghem
Instability of the human immunoglobulin heavy chain constant region locus indicated by different inherited chromosomal deletions.
Molecular biology & medicine 1983;1(2):207-17.
1983: A N Helal; Gérard Lefranc; G Hauptmann; J Goetz; M M Tongio; Christian Davrinche; C Rivat; B Cavelier; J Chibani; H Chaabani
HLA A*, B*-BF* and C4 A*, B* allele associations, with special reference to BF*S07, in the Tunisian population.
Journal of immunogenetics 1983;10(3):205-8.
1983: Gérard Lefranc; H Chaabani; E Van Loghem; M P Lefranc; G De Lange; A N Helal
Simultaneous absence of the human IgG1, IgG2, IgG4 and IgA1 subclasses: immunological and immunogenetical considerations.
European journal of immunology 1983;13(3):240-4.
1982: M P Lefranc; Gérard Lefranc; T H Rabbitts
Inherited deletion of immunoglobulin heavy chain constant region genes in normal human individuals.
Nature 1982;300(5894):760-2.
1982: Gérard Lefranc; M P Lefranc; A N Helal; K Boukef; H Chaabani; M S Gandoura; E van Loghem
Unusual heavy chains of human IgG immunoglobulins: rearrangements of the ch domain exons.
Journal of immunogenetics 1982;9(1):1-9.
1982: E van Loghem; G de Lange; A M van Leeuwen; P H van Eede; L E Nijenhuis; M P Lefranc; Gérard Lefranc
Human IgG allotypes co-occurring in more than one IgG subclass.
Vox sanguinis 1982;43(6):301-9.
1981: M P Lefranc; Gérard Lefranc; M Farhat; R Jmour; K Boukef; Y Beuzard; F Galacteros; J Rosa
Frequency of human A gamma 75Thr globin chain in a population from Tunisia.
Human genetics 1981;59(1):89-91.
1981: M P Lefranc; J Chibani; A N Helal; K Boukef; J Seger; Gérard Lefranc
Human transferrin (Tf) and group-specific component (Gc) subtypes in Tunisia.
Human genetics 1981;59(1):60-3.
1981: Gérard Lefranc; M P Lefranc; J Seger; J P Salier; L Chakhachiro; J Loiselet
Sex limited ahaptoglobinaemia.
Human genetics 1981;58(3):294-7.
1981: Christian Davrinche; C Rivat; L Rivat-Peran; A N Helal; K Boukef; M P Lefranc; Gérard Lefranc
Genetic variants of human C3 and properdin factor B in a population from Tunisia.
Human heredity 1981;31(5):299-303.
1980: E van Loghem; Rem I Sukernik; Ludmila P Osipova; B J Zegers; H Matsumoto; G de Lange; Gérard Lefranc
Gene deletion and gene duplication within the cluster of human heavy-chain genes. Selective absence of IgG sub-classes.
Journal of immunogenetics 1980;7(4):285-99.
1980: Gérard Lefranc; M P Lefranc
Discontinuous genes and DNA sequence transposition: a model for immunoglobulin chain synthesis.
Journal of immunogenetics 1980;7(3):207-14.
1980: J P Salier; L Rivat; M Daveau; Gérard Lefranc; P Breton; C H de Menibus; A Henocq; H H Fudenberg
Quantitative studies of Gm allotypes. V. Simultaneous presence of latent Gm allotypes and deficient Gm genes in a family with hypogammaglobulinaemic probands.
Journal of immunogenetics 1980;7(2):123-35.
1979: J L Serre; Gérard Lefranc; J Loiselet; A Jacquard
HLA markers in six Lebanese religious subpopulations.
Tissue antigens 1979;14(3):251-5.
1979: Gérard Lefranc; S M Dumitresco; J P Salier; L Rivat; G de Lange; E van Loghem; J Loiselet
Familial lack of the IgG3 subclass: gene elimination or turning off expression and neutral evolution in the immune system.
Journal of immunogenetics 1979;6(4):215-21.
1979: Gérard Lefranc; G de Lange; L Rivat; A Langaney; M P Lefranc; F Ellouze; G Sfar; M Sfar; E van Loghem
Gm, Am and Km immunoglobulin allotypes of two populations in Tunisia.
Human genetics 1979;50(2):199-211.
1978: Gérard Lefranc; L Rivat; J L Serre; J M Lalouel; G Pison; J Loiselet; C Ropartz; G de Lange; E van Loghem
Common and uncommon immunoglobulin haplotypes among Lebanese communities.
Human genetics 1978;41(2):197-209.
1977: Gérard Lefranc; L Rivat; J P Salier; E van Loghem; H Aydenian; P Zalzal; L Chakhachiro; J Loiselet; C Ropartz
Recombination, mutation, or constitutive expression at a Gm locus and familial hypergammaglobulinemia.
American journal of human genetics 1977;29(5):523-36.
1976: R S Geha; A Malakian; Gérard Lefranc; D Chayban; J L Serre
Immunologic reconstitution in severe combined immunodeficiency following transplantation with parental bone marrow.
Pediatrics 1976;58(3):451-5.