SA
Saadia Amasdl

Publications (3)

Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease
Article scientifique · 2017
20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature
Article scientifique · 2016
Insulin-like growth factor type 1 deficiency in a Moroccan patient with de novo inverted duplication 9p24p12 and developmental delay: a case report
Article scientifique · 2016

Domaines principaux

Sciences de la vie et biotechnologies2 Sciences de la santé1

Statistiques

Consultations11
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