Articles with "hypothyroidism frequent" as a keyword



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A frequent oligogenic involvement in congenital hypothyroidism.

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Published in 2017 at "Human molecular genetics"

DOI: 10.1093/hmg/ddx145

Abstract: Congenital hypothyroidism (CH), the most frequent form of preventable mental retardation, is predicted to have a relevant genetic origin. However, CH is frequently reported to be sporadic and candidate gene variations were found in  read more here.

Keywords: oligogenic involvement; congenital hypothyroidism; candidate genes; hypothyroidism frequent ... See more keywords