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Rafaëlle Bernard
Rafaëlle Bernard
French Institute of Health and Medical Research
Facioscapulohumeral muscular dystrophy
Biology
Genetics
Endocrinology
Pathology
2
Papers
12
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0
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Inflammatory facioscapulohumeral muscular dystrophy type 2 in 18p deletion syndrome
2018
American Journal of Medical Genetics Part A
Dimitri Renard
Guillaume Taieb
Matteo Garibaldi
André Maues De Paula
Rafaëlle Bernard
Nadira Lagha
Gaël Cristofari
Catherine Vovan
Charlene Chaix
Nicolas Lévy
Philippe Khau Van Kien
Sabrina Sacconi
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Citations (3)
New multiplex PCR-based protocol allowing indirect diagnosis of FSHD on single cells: can PGD be offered despite high risk of recombination?
2010
European Journal of Human Genetics
Mouna Barat-Houari
Karine Nguyen
Rafaëlle Bernard
C Fernández
Catherine Vovan
Corinne Bareil
Philippe Khau Van Kien
Delphine Thorel
Sylvie Tuffery-Giraud
Francis Vasseur
Shahram Attarian
J. Pouget
A. Girardet
Nicolas Lévy
Mireille Claustres
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Citations (9)
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