Biblio
2 resultats trouvés
Filtres: Auteur is Jacquinet, Adeline [Clear All Filters]
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2020. GREB1L variants in familial and sporadic hereditary urogenital adysplasia and Mayer-Rokitansky-Kuster-Hauser syndrome. CLINICAL GENETICS. 98:126-137.
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2014. Neonatal progeroid variant of Marfan syndrome with congenital lipodystrophy results from mutations at the 3 ` end of FBN1 gene. EUROPEAN JOURNAL OF MEDICAL GENETICS. 57:230-234.