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Marguerite Prieur

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valerie malan; Marie-Christine De Blois; Marguerite Prieur; M C Perrier-Waill; C Huguet-Nedjar; L Gegas; Catherine Turleau; Michel Vekemans; A Munnich; Serge Romana
Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene.
ML Jacquemont; Damien Sanlaville; Richard Redon; Odile Raoul; Valérie Cormier-Daire; Stanislas LYONNET; Jeanne Amiel; Martine Le Merrer; D Heron; Marie-Christine De Blois; Marguerite Prieur; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux; Anne Philippe
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
Patrick Callier; Laurence Faivre; N Marle; Christel Thauvin-Robinet; Damien Sanlaville; P Gosset; Marguerite Prieur; M Labenne; Frédéric Huet; Francine Mugneret
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization.

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2008: valerie malan; Marie-Christine De Blois; Marguerite Prieur; M C Perrier-Waill; C Huguet-Nedjar; L Gegas; Catherine Turleau; Michel Vekemans; A Munnich; Serge Romana
Sotos syndrome caused by a paracentric inversion disrupting the NSD1 gene.
Clinical genetics 2008;73(1):89-91.
2006: ML Jacquemont; Damien Sanlaville; Richard Redon; Odile Raoul; Valérie Cormier-Daire; Stanislas LYONNET; Jeanne Amiel; Martine Le Merrer; D Heron; Marie-Christine De Blois; Marguerite Prieur; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux; Anne Philippe
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disorders.
Journal of medical genetics 2006;43(11):843-9.
2006: Patrick Callier; Laurence Faivre; N Marle; Christel Thauvin-Robinet; Damien Sanlaville; P Gosset; Marguerite Prieur; M Labenne; Frédéric Huet; Francine Mugneret
Major feeding difficulties in the first reported case of interstitial 20q11.22-q12 microdeletion and molecular cytogenetic characterization.
American journal of medical genetics. Part A 2006;140A(17):1859-63.
2006: M Chaabouni; Martine Le Merrer; Odile Raoul; Marguerite Prieur; Marie-Christine De Blois; Anne Philippe; Michel Vekemans; Serge Romana
Molecular cytogenetic analysis of five 2q37 deletions: refining the brachydactyly candidate region.
European journal of medical genetics 2006;49(3):255-63.
2005: Azarnouche Ardalan; Marguerite Prieur; Agnès Choiset; Catherine Turleau; Françoise Goutieres; Sylvie Girard-Orgeolet
Intrachromosomal insertion mimicking a pericentric inversion: molecular cytogenetic characterization of a three break rearrangement of chromosome 20.
American journal of medical genetics. Part A 2005;138A(3):288-93.
2005: Damien Sanlaville; David Genevieve; Céline Bernardin; Jeanne Amiel; Clarisse Baumann; Marie-Christine De Blois; Valérie Cormier-Daire; Bénédicte Gerard; Marion Gerard; Martine Le Merrer; Philippe Parent; Fabienne Prieur; Marguerite Prieur; Odile Raoul; Annick Toutain; Alain Verloes; Géraldine Viot; Serge Romana; Arnold Munnich; Stanislas LYONNET; Michel Vekemans; Catherine Turleau
Failure to detect an 8p22-8p23.1 duplication in patients with Kabuki (Niikawa-Kuroki) syndrome.
European journal of human genetics : EJHG 2005;13(5):690-3.
2005: Damien Sanlaville; Marguerite Prieur; Marie-Christine De Blois; David Genevieve; Jean-Michel Lapierre; Catherine Ozilou; Monique Picq; Philippe Gosset; Nicole Morichon-Delvallez; Arnold Munnich; Valérie Cormier-Daire; Geneviève Baujat; Serge Romana; Michel Vekemans; Catherine Turleau
Functional disomy of the Xq28 chromosome region.
European journal of human genetics : EJHG 2005;13(5):579-85.
2005: Ilhan Tezcan; Fügen Ersoy; Ozden Sanal; Tuba Turul; Duygu Uckan; Sevim Balci; Gonul Hicsonmez; Marguerite Prieur; S Caillat-Zucmann; Francois Le Deist; Geneviève de Saint Basile
Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.
The Journal of pediatrics 2005;146(1):137-40.
2004: Guntram Borck; Richard Redon; Damien Sanlaville; Marlène Rio; Marguerite Prieur; Stanislas LYONNET; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux; Valérie Cormier-Daire
NIPBL mutations and genetic heterogeneity in Cornelia de Lange syndrome.
Journal of medical genetics 2004;41(12):e128.
2004: Guntram Borck; Marlène Rio; Damien Sanlaville; Richard Redon; Florence Molinari; Delphine Bacq; Odile Raoul; Valérie Cormier-Daire; Stanislas LYONNET; Jeanne Amiel; Martine Le Merrer; Marie-Christine De Blois; Marguerite Prieur; Michel Vekemans; Nigel P Carter; Arnold Munnich; Laurence Colleaux
Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardation.
Clinical genetics 2004;66(2):122-7.
2004: Jean-Michel Lapierre; Damien Sanlaville; J Kang; Catherine Ozilou; Marc Le Lorc'h; Marie-Christine Perrier Waill; Marguerite Prieur; Laurence Colleaux; Arnold Munnich; Catherine Turleau; Moncef Benkhalifa; M Mohammed; Michel Vekemans; Serge Romana
[A preliminary study to assess the value of the DNA chips SpectralChip to detect subtle constitutional chromosome imbalances].
Annales de biologie clinique 2004;62(2):203-12.
2003: Judith J Luciani; Philippe De Mas; Danielle Depetris; Cécile Mignon-Ravix; A Bottani; Marguerite Prieur; P Jonveaux; Anne Philippe; Georges Bourrouillou; B de Martinville; Bruno Delobel; L Vallee; Marie-Françoise Croquette; Marie-Geneviève Mattei
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations.
Journal of medical genetics 2003;40(9):690-6.
2003: Marlène Rio; L Clech; Jeanne Amiel; Laurence Faivre; Stanislas LYONNET; Martine Le Merrer; Sylvie Odent; Didier Lacombe; P Edery; Raja Brauner; Odile Raoul; Philippe Gosset; Marguerite Prieur; Michel Vekemans; Arnold Munnich; Laurence Colleaux; Valérie Cormier-Daire
Spectrum of NSD1 mutations in Sotos and Weaver syndromes.
Journal of medical genetics 2003;40(6):436-40.
2002: Laurence Faivre; Philippe Gosset; Valérie Cormier-Daire; Sylvie Odent; Jeanne Amiel; Irina Giurgea; Marie-Cécile Nassogne; Laurent Pasquier; Arnold Munnich; Serge Romana; Marguerite Prieur; Michel Vekemans; Marie-Christine De Blois; Catherine Turleau
Overgrowth and trisomy 15q26.1-qter including the IGF1 receptor gene: report of two families and review of the literature.
European journal of human genetics : EJHG 2002;10(11):699-706.
2002: Laurence Faivre; Valérie Cormier-Daire; Jean-Michel Lapierre; Laurence Colleaux; S Jacquemont; D Geneviéve; P Saunier; A Munnich; Catherine Turleau; Serge Romana; Marguerite Prieur; Marie-Christine De Blois; Michel Vekemans
Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype.
Journal of medical genetics 2002;39(8):594-6.
2002: Marlène Rio; Florence Molinari; Solange Heuertz; Catherine Ozilou; Philippe Gosset; Odile Raoul; Valérie Cormier-Daire; Jeanne Amiel; Stanislas LYONNET; Martine Le Merrer; Catherine Turleau; Marie-Christine De Blois; Marguerite Prieur; Serge Romana; Michel Vekemans; Arnold Munnich; Laurence Colleaux
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardation.
Journal of medical genetics 2002;39(4):266-70.
2001: André Mégarbané; Philippe Gosset; Noëlle Souraty; Jean-Michel Lapierre; R Korban; Laila Zahed; L Samaras; Michel Vekemans; Marguerite Prieur
Chromosome 10p11.2-p12.2 duplication: report of a patient and review of the literature.
American journal of medical genetics 2001;104(3):204-8.
2001: Jeanne Amiel; Yolanda Espinosa-Parrilla; Julie Steffann; P Gosset; Anna Pelet; Marguerite Prieur; Odile Boute; A Choiset; Didier Lacombe; N Philip; Martine Le Merrer; H Tanaka; M Till; Renaud Touraine; Annick Toutain; Michel Vekemans; Arnold Munnich; Stanislas LYONNET
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures.
American journal of human genetics 2001;69(6):1370-7.
2001: G Joly; Jean-Michel Lapierre; Catherine Ozilou; Philippe Gosset; A Aurias; Marie-Christine De Blois; Marguerite Prieur; Odile Raoul; Laurence Colleaux; Arnold Munnich; Serge Romana; Michel Vekemans; Catherine Turleau
Comparative genomic hybridisation in mentally retarded patients with dysmorphic features and a normal karyotype.
Clinical genetics 2001;60(3):212-9.
2001: Marlène Rio; Catherine Ozilou; Valérie Cormier-Daire; Catherine Turleau; Marguerite Prieur; Michel Vekemans; P Chauveau; Arnold Munnich; Laurence Colleaux
Partial maternal heterodisomy of chromosome 17q25 in a case of severe mental retardation.
Human genetics 2001;108(6):511-5.
2001: Laurence Colleaux; Marlène Rio; Solange Heuertz; S Moindrault; Catherine Turleau; Catherine Ozilou; Philippe Gosset; O Raoult; Stanislas LYONNET; Valérie Cormier-Daire; Jeanne Amiel; Martine Le Merrer; Monique Picq; Marie-Christine De Blois; Marguerite Prieur; Serge Romana; F Cornelis; Michel Vekemans; Arnold Munnich
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardation.
European journal of human genetics : EJHG 2001;9(5):319-27.
2001: André Mégarbané; Marc Le Lorc'h; Hatem Elghezal; G Joly; Noëlle Souraty; L Samaras; Marguerite Prieur; Michel Vekemans; Catherine Turleau; Serge Romana
Pure partial 7p trisomy including the TWIST, HOXA, and GLI3 genes.
Journal of medical genetics 2001;38(3):178-82.
2000: André Mégarbané; Philippe Gosset; Noëlle Souraty; Jean-Michel Lapierre; Catherine Turleau; Michel Vekemans; Jacques Loiselet; Marguerite Prieur
Chromosome 7q22-q31 duplication: report of a new case and review.
American journal of medical genetics 2000;95(2):164-8.
2000: Sandra Fert-Ferrer; Agnès Guichet; Julia Tantau; Anne-Lise Delezoide; Catherine Ozilou; Serge Romana; Philippe Gosset; Géraldine Viot; S Loison; Claude Moraine; Nicole Morichon-Delvallez; Catherine Turleau; Michel Vekemans; Marguerite Prieur
Subtle familial unbalanced translocation t(8;11)(p23.2;p15.5) in two fetuses with Beckwith-Wiedemann features.
Prenatal diagnosis 2000;20(6):511-5.
2000: Laurence Faivre; Géraldine Viot; Marguerite Prieur; Catherine Turleau; P Gosset; Serge Romana; Arnold Munnich; M Vekemans; Valérie Cormier-Daire
Apparent Sotos syndrome (cerebral gigantism) in a child with trisomy 20p11.2-p12.1 mosaicism.
American journal of medical genetics 2000;91(4):273-6.
1999: R Dufourcq-Lagelouse; N Lambert; M Duval; Géraldine Viot; Etienne Vilmer; Alain Fischer; Marguerite Prieur; Geneviève de Saint Basile
Chediak-Higashi syndrome associated with maternal uniparental isodisomy of chromosome 1.
European journal of human genetics : EJHG 1999;7(6):633-7.
1998: G Viot-Szoboszlai; Jeanne Amiel; François Doz; Marguerite Prieur; J Couturier; J N Zucker; I Henry; Arnold Munnich; Michel Vekemans; Stanislas LYONNET
Wilms' tumor and gonadal dysgenesis in a child with the 2q37.1 deletion syndrome.
Clinical genetics 1998;53(4):278-80.
1997: Pascale De Lonlay-Debeney; Valérie Cormier-Daire; Jeanne Amiel; Véronique Abadie; Sylvie Odent; Alain Paupe; Sophie Couderc; AL Tellier; Damien Bonnet; Marguerite Prieur; Michel Vekemans; Arnold Munnich; Stanislas LYONNET
Features of DiGeorge syndrome and CHARGE association in five patients.
Journal of medical genetics 1997;34(12):986-9.
1997: AK Ryan; Judith A Goodship; David I Wilson; N Philip; A Levy; Heide Seidel; S Schuffenhauer; H Oechsler; B Belohradsky; Marguerite Prieur; A Aurias; F L Raymond; Jill Clayton-Smith; E Hatchwell; Carole M E McKeown; F A Beemer; B Dallapiccola; G Novelli; Jane A Hurst; Jaakko Ignatius; A J Green; Robin M Winter; Louise A Brueton; K Brøndum-Nielsen; Peter J Scambler
Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.
Journal of medical genetics 1997;34(10):798-804.
1997: André Mégarbané; Noëlle Souraty; Marguerite Prieur; D Theophile; P Chédid; J Augé; Michel Vekemans
Interstitial duplication of the short arm of chromosome 2: report of a new case and review.
Journal of medical genetics 1997;34(9):783-6.
1997: KA Rack; F Cornélis; Isabelle Radford-Weiss; Alain BERNHEIM; C J Harrison; Olivier Hermine; Marguerite Prieur; Michel Vekemans; Elizabeth Macintyre
A chromosome 14q11/TCR alpha/delta specific yeast artificial chromosome improves the detection rate and characterization of chromosome abnormalities in T-lymphoproliferative disorders.
Blood 1997;90(3):1233-40.
1997: Valérie Cormier-Daire; Martine Le Merrer; Nadine Gigarel; N Morichon; Marguerite Prieur; Stanislas LYONNET; Michel Vekemans; Arnold Munnich
Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome.
American journal of medical genetics 1997;69(2):166-8.
1997: M Mathieu; C Piussan; François Thepot; A Gouget; Didier Lacombe; Jean-Michel Pedespan; F Serville; D Fontan; M Ruffie; Annie Nivelon-Chevallier; F Amblard; P Chauveau; H Moirot; J P Chabrolle; Marie-Françoise Croquette; M Teyssier; H Plauchu; M C Pelissier; S Gilgenkrantz; C Turc-Carel; Catherine Turleau; Marguerite Prieur; M Le Merrer; M Gonzales; Hubert Journel
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children).
Annales de génétique 1997;40(1):45-54.
1996: Michel Bahuau; W Flintoff; B Assouline; Stanislas LYONNET; Martine Le Merrer; Marguerite Prieur; M Guilloud-Bataille; N Feingold; Arnold Munnich; M Vidaud; Dominique Vidaud
Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.
American journal of medical genetics 1996;66(3):347-55.
1995: Z Chettouh; Marie-Françoise Croquette; Bruno Delobel; S Gilgenkrants; C Leonard; C Maunoury; Marguerite Prieur; M O Rethoré; Pierre-Marie Sinet; M Chery
Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.
American journal of human genetics 1995;57(1):62-71.
1995: S Demczuk; A Lévy; M Aubry; Marie-Françoise Croquette; N Philip; Marguerite Prieur; U Sauer; Patrice Bouvagnet; Guy Rouleau; Gilles Thomas
Excess of deletions of maternal origin in the DiGeorge/velo-cardio-facial syndromes. A study of 22 new patients and review of the literature.
Human genetics 1995;96(1):9-13.
1994: Constantinos Pangalos; Dimitrios Avramopoulos; Jean-Louis Blouin; O Raoul; M C deBlois; Marguerite Prieur; Albert Schinzel; M Gika; Danae Abazis; Stylianos Antonarakis
Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis.
American journal of human genetics 1994;54(3):473-81.
1994: Pierre-Marie Sinet; D Théophile; Z Rahmani; Z Chettouh; Jean-Louis Blouin; Marguerite Prieur; B Noel; Jean-Maurice Delabar
Mapping of the Down syndrome phenotype on chromosome 21 at the molecular level.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 1994;48(5-6):247-52.
1994: S Demczuk; C Desmaze; M Aikem; Marguerite Prieur; F Ledeist; M Sanson; Guy Rouleau; Gilles Thomas; Alain Aurias
Molecular cytogenetic analysis of a series of 23 DiGeorge syndrome patients by fluorescence in situ hybridization.
Annales de génétique 1994;37(2):60-5.
1993: C Desmaze; Marguerite Prieur; F Amblard; M Aikem; F LeDeist; S Demczuk; J Zucman; B Plougastel; Olivier Delattre; Marie-Françoise Croquette
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.
American journal of human genetics 1993;53(6):1239-49.
1993: Marc Jeanpierre; C Turleau; Alain Aurias; Marguerite Prieur; F Ledeist; Alain Fischer; E Viegas-Pequignot
An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome.
Human molecular genetics 1993;2(6):731-5.
1993: C Desmaze; Peter J Scambler; Marguerite Prieur; Stephanie Halford; D Sidi; F Le Deist; Alain Aurias
Routine diagnosis of DiGeorge syndrome by fluorescent in situ hybridization.
Human genetics 1993;90(6):663-5.
1993: Pierre-Marie Sinet; D Théophile; Z Rahmani; Z Chettouh; Jean-Louis Blouin; Marguerite Prieur; B Noel; Jean-Maurice Delabar
Molecular mapping of the Down syndrome phenotype on chromosome 21.
Progress in clinical and biological research 1993;384():63-86.
1993: Jean-Maurice Delabar; D Theophile; Z Rahmani; Z Chettouh; Jean-Louis Blouin; Marguerite Prieur; B Noel; Pierre-Marie Sinet
Molecular mapping of twenty-four features of Down syndrome on chromosome 21.
European journal of human genetics : EJHG 1993;1(2):114-24.
1992: Constantinos Pangalos; D Théophile; Pierre-Marie Sinet; A Marks; D Stamboulieh-Abazis; Z Chettouh; Marguerite Prieur; C Verellen; M O Rethoré; J Lejeune
No significant effect of monosomy for distal 21q22.3 on the Down syndrome phenotype in "mirror" duplications of chromosome 21.
American journal of human genetics 1992;51(6):1240-50.
1992: M Poissonnier; C Turleau; M Olivier-Martin; M J Milleret-Proyart; Marguerite Prieur; M Dubos; M O Cabanis; F Mugneret; P Blanc; L Noel
Interstitial deletion of the proximal region of the long arm of chromosome 18, del(18q12) a distinct clinical entity? A report of two new cases.
Annales de génétique 1992;35(3):146-51.
1992: Yurgos Remvikos; Michelle Gerbault-Seureau; Henri Magdelénat; Marguerite Prieur; Bernard Dutrillaux
Proliferative activity of breast cancers increases in the course of genetic evolution as defined by cytogenetic analysis.
Breast cancer research and treatment 1992;23(1-2):43-9.
1992: Henri Magdelenat; Michelle Gerbault-Seureau; C Laine-Bidron; Marguerite Prieur; Bernard Dutrillaux
Genetic evolution of breast cancer: II. Relationship with estrogen and progesterone receptor expression.
Breast cancer research and treatment 1992;22(2):119-27.
1991: Jean-Louis Blouin; Alain Aurias; N Créau-Goldberg; F Apiou; C Alcaide-Loridan; A Bruel; Marguerite Prieur; J Kraus; Jean-Maurice Delabar; Pierre-Marie Sinet
Cytogenetic and molecular analysis of a de novo tandem duplication of chromosome 21.
Human genetics 1991;88(2):167-74.
1991: A Bruel; G Cherqui; S Columelli; D Margelin; M Roudier; Pierre-Marie Sinet; Marguerite Prieur; J L Pérignon; Jean-Maurice Delabar
Reduced protein kinase C activity in sporadic Alzheimer's disease fibroblasts.
Neuroscience letters 1991;133(1):89-92.
1991: Bernard Dutrillaux; Michelle Gerbault-Seureau; Yurgos Remvikos; Brigitte Zafrani; Marguerite Prieur
Breast cancer genetic evolution: I. Data from cytogenetics and DNA content.
Breast cancer research and treatment 1991;19(3):245-55.
1991: B Dutrillaux; Michelle Gerbault-Seureau; Brigitte Zafrani; Marguerite Prieur
Prolonged G2 phase of breast cancer cells and chromosome damage.
European journal of cancer (Oxford, England : 1990) 1991;27(10):1307-12.
1990: Jean-Louis Blouin; Z Rahmani; Z Chettouh; Marguerite Prieur; J Fermanian; M Poissonnier; C Leonard; Annie Nicole; J F Mattei; Pierre-Marie Sinet
Slot blot method for the quantification of DNA sequences and mapping of chromosome rearrangements: application to chromosome 21.
American journal of human genetics 1990;46(3):518-26.
1990: L Massaad; Marguerite Prieur; C Leonard; Bernard Dutrillaux
Biclonal chromosome evolution of chronic myelomonocytic leukemia in a child.
Cancer genetics and cytogenetics 1990;44(1):131-7.
1990: Z Rahmani; Jean-Louis Blouin; N Créau-Goldberg; P C Watkins; J F Mattei; M Poissonnier; Marguerite Prieur; Z Chettouh; Annie Nicole; Alain Aurias
Down syndrome critical region around D21S55 on proximal 21q22.3.
American journal of medical genetics. Supplement 1990;7():98-103.
1989: Z Rahmani; Jean-Louis Blouin; N Creau-Goldberg; P C Watkins; J F Mattei; M Poissonnier; Marguerite Prieur; Z Chettouh; Annie Nicole; Alain Aurias
Critical role of the D21S55 region on chromosome 21 in the pathogenesis of Down syndrome.
Proceedings of the National Academy of Sciences of the United States of America 1989;86(15):5958-62.
1989: L Massaad; Marguerite Prieur; C Gaud; A Fischer; Bernard Dutrillaux
Unusual karyotypic evolution in subacute myelomonocytic leukemia in two monozygotic twins.
Cancer genetics and cytogenetics 1989;38(2):205-13.
1989: C Turleau; M O Cabanis; D Girault; F Ledeist; R Mettey; H Puissant; Marguerite Prieur; J de Grouchy
Multibranched chromosomes in the ICF syndrome: immunodeficiency, centromeric instability, and facial anomalies.
American journal of medical genetics 1989;32(3):420-4.
1989: Z Mamuris; Marguerite Prieur; Bernard Dutrillaux; Alain Aurias
Specificity of melphalan-induced rearrangements and their transmission through cell divisions.
Mutagenesis 1989;4(2):133-9.
1989: R Aledo; G Renault; Marguerite Prieur; M F Avril; B Chrétien; Bernard Dutrillaux; Alain Aurias
Increase of sister chromatid exchanges in excision repair deficient xeroderma pigmentosum.
Human genetics 1989;81(3):221-5.
1989: Z Mamuris; Michelle Gerbault-Seureau; Marguerite Prieur; Pierre Pouillart; Bernard Dutrillaux; Alain Aurias
Chromosomal aberrations in lymphocytes of patients treated with melphalan.
International journal of cancer. Journal international du cancer 1989;43(1):80-6.
1989: Z Mamuris; Marguerite Prieur; Bernard Dutrillaux; Alain Aurias
The chemotherapeutic drug melphalan induces breakage of chromosomes regions rearranged in secondary leukemia.
Cancer genetics and cytogenetics 1989;37(1):65-77.
1988: Marguerite Prieur; W Al Achkar; Alain Aurias; Jérôme Couturier; Anne-Marie Dutrillaux; Bernard Dutrillaux; A Flüry-Herard; Michelle Gerbault-Seureau; F Hoffschir; E Lamoliatte
Acquired chromosome rearrangements in human lymphocytes: effect of aging.
Human genetics 1988;79(2):147-50.
1988: F Hoffschir; Marguerite Prieur; B Dutrillaux
Diagrammatic representation for chromosomal mutagenesis studies. IV. Radiation-induced rearrangements in Ateles sp. (Primate, Platyrhini).
Mutation research 1988;199(1):103-10.
1987: S Gilgenkrantz; J P Fryns; P Droulle; M Schweitzer; B Chadefaux; Marguerite Prieur
[Mosaic tetrasomy 12p. Identical nature of the Pallister syndrome, the Teschler-Nicola/Killian syndrome and mosaic tetrasomy 21].
Journal de génétique humaine 1987;35(1):51-61.
1985: S Gilgenkrantz; P Droulle; M Schweitzer; B Foliguet; B Chadefaux; M Lombard; M Chery; Marguerite Prieur
Mosaic tetrasomy 12p.
Clinical genetics 1985;28(6):495-502.
1985: Alain Aurias; Jérôme Couturier; Anne-Marie Dutrillaux; Bernard Dutrillaux; F Herpin; E Lamoliatte; M Lombard; Martine Muleris; M Paravatou; Marguerite Prieur
Inversion (14)(q12qter) or (q11.2q32.3): the most frequently acquired rearrangement in lymphocytes.
Human genetics 1985;71(1):19-21.
1982: B Dutrillaux; A Aurias; Anne-Marie Dutrillaux; D Buriot; Marguerite Prieur
The cell cycle of lymphocytes in Fanconi anemia.
Human genetics 1982;62(4):327-32.
1981: B Dutrillaux; E Viegas Pequignot; Alain Aurias; M Prod'homme; M Sportes; Marguerite Prieur
Tentative estimate of the risk of chromosomal disease due to radiation-induced translocations in man.
Mutation research 1981;82(1):191-200.