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Françoise Baverel

Research Profile

Disorders

Procedures

Anatomy

Chromosomes, Human, X

Physiology

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Publications

TOP 3
Aziza Lebbar; Patrick Callier; Françoise Baverel; Nathalie Marle; Catherine Patrat; Dominique Le Tessier; Francine Mugneret; Jean-Michel Dupont
Two cases of mosaicism for complex chromosome rearrangements (CCRM) associated with secondary infertility.
Celine Dupont; Aziza Lebbar; Cecile Teinturier; Françoise Baverel; Géraldine Viot; Dominique Le Tessier; Jerome Le Bozec; Laurence Cuisset; Jean-Michel Dupont
First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation.
Mohammad Pazooki; Aziza Lebbar; Anne Roubergues; Françoise Baverel; Dominique Letessier; Jean-Michel Dupont
Pure familial 6q21q22.1 duplication in two generations.

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All Publications

2008: Aziza Lebbar; Patrick Callier; Françoise Baverel; Nathalie Marle; Catherine Patrat; Dominique Le Tessier; Francine Mugneret; Jean-Michel Dupont
Two cases of mosaicism for complex chromosome rearrangements (CCRM) associated with secondary infertility.
American journal of medical genetics. Part A 2008;146A(20):2651-6.
2007: Celine Dupont; Aziza Lebbar; Cecile Teinturier; Françoise Baverel; Géraldine Viot; Dominique Le Tessier; Jerome Le Bozec; Laurence Cuisset; Jean-Michel Dupont
First reported case of intrachromosomal cryptic inv dup del Xp in a boy with developmental retardation.
American journal of medical genetics. Part A 2007;143A(11):1236-43.
2007: Mohammad Pazooki; Aziza Lebbar; Anne Roubergues; Françoise Baverel; Dominique Letessier; Jean-Michel Dupont
Pure familial 6q21q22.1 duplication in two generations.
European journal of medical genetics 2007;50(1):60-5.
2003: Catherine Dodé; Jacqueline Levilliers; Jean-Michel Dupont; Anne De Paepe; Nathalie Le Dû; Nadia Soussi-Yanicostas; Roney Coimbra; Sedigheh Delmaghani; Sylvie Compain-Nouaille; Françoise Baverel; Christophe Pêcheux; Dominique Le Tessier; Corinne Cruaud; Marc Delpech; Frank Speleman; Stefan Vermeulen; Andrea Amalfitano; Yvan Bachelot; Philippe Bouchard; Sylvie Cabrol; Jean-Claude Carel; Henriette A Delemarre-Van De Waal; Barbara Goulet-Salmon; Marie-Laure Kottler; Odile Richard; Franco Sanchez-Franco; Robert Saura; Jacques Young; Christine Petit; Jean-Pierre Hardelin
Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.
Nature genetics 2003;33(4):463-5.
2002: Aziza Lebbar; Géraldine Viot; S Szpiro-Tapia; Françoise Baverel; Didier Rabineau; Jean-Michel Dupont
Pregnancy outcome following prenatal diagnosis of an isodicentric X chromosome: first case report.
Prenatal diagnosis 2002;22(11):973-5.
1998: T Thevenot; Robin Dhote; Micheline Tulliez; Françoise Baverel; S Permal; Didier Rabineau; Boyan Christoforov
[Turner syndrome and nodular regenerative hyperplasia of the liver].
Annales de médecine interne 1998;149(5):295-6.
1997: Jean-Michel Dupont; Dominique Le Tessier; Françoise Baverel; A Rouffet; Didier Rabineau
Mosaic isochromosome 20q and normal outcome: a new case ascertained by fluorescence in situ hybridization and a review of the literature.
Fetal diagnosis and therapy 1997;12(5):283-5.
1985: Françoise Baverel; J de Recondo; A Rouffet; D Fredy; A Salesses; P Rondot
[Agenesis of the corpus callosum in a man with complete mosaic trisomy 8].
Presse médicale (Paris, France : 1983) 1985;14(14):781-3.
1985: A Salesses; B Asselain; Françoise Baverel; Didier Rabineau
[Effects of castration on the development of the juxtaglomerular apparatus in the albino rat during growth].
Archives d'anatomie, d'histologie et d'embryologie normales et expérimentales 1985;68():61-8.
1981: A Salesses; A Boissonnas; A Rouffet; Françoise Baverel; R Caquet; P Bugard; C Laroche
[X short arm deletion and Turner syndrome. A new case 46, X, del (X) (p11) (author's transl)].
Annales d'endocrinologie 1981;42(2):147-51.