HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2; CHNG2

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Summary

Literature (2)

Literature for OMIM 218700: HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 2; CHNG2

Xenbase Articles:
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Denotes literature images)

Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism., Vick P,Eberle B,Choukair D,Weiss B,Roeth R,Schneider I,Paramasivam N,Bettendorf M,Rappold GA, Genes (Basel). November 24, 2021; 12(12):2073-4425.
Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. October 13, 2023; :1552-5015.

Identification of ZBTB26 as a Novel Risk Factor for Congenital Hypothyroidism., Vick P,Eberle B,Choukair D,Weiss B,Roeth R,Schneider I,Paramasivam N,Bettendorf M,Rappold GA, Genes (Basel). November 24, 2021; 12(12):2073-4425.

Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes., Neal SJ,Rajasekaran A,Jusić N,Taylor L,Read M,Alfandari D,Alfandari D,Pignoni F,Moody SA, J Exp Zool B Mol Dev Evol. October 13, 2023; :1552-5015.