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Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant

Fuente: Wiley Open Access

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Détails bibliographiques
Auteurs principaux:	Carly M. Smith, Kristi Guinon, Suha Bachir, Christina G. Tise
Format:	Artículo Open Access
Publié:	Wiley 2024
Sujets:	Prenatal Diagnosis
Accès en ligne:	Acceder al recurso
Tags:	Ajouter un tag Pas de tags, Soyez le premier à ajouter un tag!

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