Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome

BACKGROUND: Congenital heart disease (CHD) is a cardinal feature of X chromosome monosomy, or Turner syndrome (TS). Haploinsufficiency for gene(s) located on Xp have been implicated in the short stature characteristic of the syndrome, but the chromosomal region related to the CHD phenotype has not b...

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Detalles Bibliográficos
Autores principales: Bondy, Carolyn, Bakalov, Vladimir K, Cheng, Clara, Olivieri, Laura, Rosing, Douglas R, Arai, Andrew E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2013
Materias:
Developmental Defects
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786649/
https://www.ncbi.nlm.nih.gov/pubmed/23825392
http://dx.doi.org/10.1136/jmedgenet-2013-101720

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3786649/
https://www.ncbi.nlm.nih.gov/pubmed/23825392
http://dx.doi.org/10.1136/jmedgenet-2013-101720

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