Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome

BACKGROUND: We report a consanguineous couple that has experienced three consecutive pregnancy losses following the foetal ultrasound finding of short limbs. Post-termination examination revealed no skeletal dysplasia, but some subtle proximal limb shortening in two foetuses, and a spectrum of mildl...

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Detalles Bibliográficos
Autores principales: Marshall, Christian R, Farrell, Sandra A, Cushing, Donna, Paton, Tara, Stockley, Tracy L, Stavropoulos, Dimitri J, Ray, Peter N, Szego, Michael, Lau, Lynette, Pereira, Sergio L, Cohn, Ronald D, Wintle, Richard F, Abuzenadah, Adel M, Abu-Elmagd, Muhammad, Scherer, Stephen W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315153/
https://www.ncbi.nlm.nih.gov/pubmed/25923536
http://dx.doi.org/10.1186/1471-2164-16-S1-S12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4315153/
https://www.ncbi.nlm.nih.gov/pubmed/25923536
http://dx.doi.org/10.1186/1471-2164-16-S1-S12

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