C. Vincent-Delorme

Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS) (2005)

Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...

Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) (2005)

Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...

Craniofrontonasal syndrome (CFNS) is an X-linked disorder characterized by a more severe manifestation in heterozygous females than in hemizygous males. Heterozygous females have craniofrontonasal...

Twenty-six novel EFNB1 mutations in familial and sporadic cranlofrontonasal syndrome (CFNS) (2005)

Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...

Craniofrontonasal syndrome (CFNS) is an X-linked disorder characterized by a more severe manifestation in heterozygous females than in hemizygous males. Heterozygous females have craniofrontonasal...

Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS) (2005)

Wieland, I., Reardon, W., Jakubiczka, S., Franco, B., Kress, W., Vincent-Delorme, C., ...

The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency

Chol, M, Lebon, S, Benit, P, Chretien, D, De Lonlay, P, Goldenberg, A, ...