Reference center spina bifida
Martani Lombard(Centre Hospitalier Universitaire de Rennes), Philippe Violas(Centre Hospitalier Universitaire de Rennes), R Brissot(Centre Hospitalier Universitaire de Rennes), Laurent Siproudhis(Hôpital Pontchaillou), P Châtellier(Centre Hospitalier Universitaire de Rennes), Hubert Journel(Centre hospitalier Bretagne Atlantique), I. Berkelmans(Centre Hospitalier Universitaire de Rennes), Marie Joncquel-Chevalier Curt(Centre Hospitalier Universitaire de Rennes), Philippe Poulain, B. Frémont(Centre Hospitalier Universitaire de Rennes), S. Odent(CIC Rennes), J. Guarniéri(Centre Hospitalier de Valenciennes), G. B(Centre Hospitalier Universitaire de Rennes), A. Manunta(Centre Hospitalier Universitaire de Rennes), Abderrahmane Hamlat(Centre Hospitalier Universitaire de Rennes), J. Kerdraon(Centre Hospitalier Universitaire de Rennes)
Cited by 0
Related Papers
SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations
|European Journal of Human Genetics|2006|244
Mutation update for the <i>CSB</i> / <i>ERCC6</i> and <i>CSA</i> / <i>ERCC8</i> genes involved in Cockayne syndrome
|Human Mutation|2009|231
Value of immunohistochemical Ki-67 and p53 determinations as predictive factors of outcome in renal cell carcinoma
|Urology|2000|130
Perinatal‐lethal Gaucher disease
|American Journal of Medical Genetics Part A|2003|127
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects
|Human Molecular Genetics|2013|112