Résultats de la recherche

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(1 - 7 of 7)
Albinism in a patient with mutations at both the OA1 and OCA3 loci
Prevention in perinatal care : an intercultural comparative research about women and men's expectation during the prenatal period in a preventive approach of parental education
Exome sequencing of Bardet-Biedl syndrome patient identifies a null mutation in the BBSome subunit BBIP1 (BBS18)
Mesoaxial polydactyly is a major feature in Bardet-Biedl syndrome patients with LZTFL1 (BBS17) mutations

Islandora displays