The Opitz syndrome gene product MID1 assembles a microtubule-associated ribonucleoprotein complex

Opitz BBB/G syndrome (OS) is a heterogenous malformation syndrome mainly characterised by hypertelorism and hypospadias. In addition, patients may present with several other defects of the ventral midline such as cleft lip and palate and congenital heart defects. The syndrome-causing gene encodes th...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Aranda-Orgillés, Beatriz, Trockenbacher, Alexander, Winter, Jennifer, Aigner, Johanna, Köhler, Andrea, Jastrzebska, Ewa, Stahl, Joachim, Müller, Eva-Christina, Otto, Albrecht, Wanker, Erich E., Schneider, Rainer, Schweiger, Susann
Formato: Artigo
Idioma:Inglês
Publicado em: Springer-Verlag 2008
Assuntos:
Original Investigation
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3774420/
https://ncbi.nlm.nih.gov/pubmed/18172692
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00439-007-0456-6
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados