Whole exome sequencing identifies mutations in 10% of familial non-syndromic cleft lip and/or palate patients in genes mutated in well-known syndromes - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue European Journal of Human Genetics Année : 2019

Whole exome sequencing identifies mutations in 10% of familial non-syndromic cleft lip and/or palate patients in genes mutated in well-known syndromes

, (1, 2) , , , , (3) , (4, 2) , , (5) ,
1
2
3
4
5
Fichier non déposé

Dates et versions

hal-03598600 , version 1 (05-03-2022)

Identifiants

  • HAL Id : hal-03598600 , version 1

Citer

M. Basha, Bénédicte Demeer, N. Revencu, S. Theys, S. Bou Saba, et al.. Whole exome sequencing identifies mutations in 10% of familial non-syndromic cleft lip and/or palate patients in genes mutated in well-known syndromes. European Journal of Human Genetics, 2019, 27 (1), pp.100. ⟨hal-03598600⟩

Collections

U-PICARDIE CHIMERE
11 Consultations
0 Téléchargements

Partager

Gmail Facebook Twitter LinkedIn More