HSPA6: A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum

BACKGROUND -: The VATER/VACTERL association refers to the non-random co-occurrence of at least three of the following component features (CFs): vertebral defects (V), anorectal malformations (ARM) (A), cardiac defects (C), tracheoesophageal fistula with or without esophageal atresia (TE), renal malf...

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Détails bibliographiques
Publié dans:Birth Defects Res
Auteurs principaux: Kause, Franziska, Zhang, Rong, Ludwig, Michael, Schmiedeke, Eberhard, Rissmann, Anke, Thiele, Holger, Altmueller, Janine, Herms, Stefan, Hilger, Alina C., Hildebrandt, Friedhelm, Reutter, Heiko
Format: Artigo
Langue:Inglês
Publié: 2019
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Article
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC6662190/
https://ncbi.nlm.nih.gov/pubmed/30887706
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdr2.1493
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