A novel mutation in thyrotropin (thyroid-stimulating hormone) gene in congenital hypothyroidism

Author:

Nirupam Nilay,Maheshwari Anu,Gupta Shelly,Aneja Satinder,Seth Anju

Publisher

Walter de Gruyter GmbH

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. syndrome and genetic defects in thyroid hormone synthesis;Kopp;Rev Endocrinol Metab Dis,2000

2. MALT lymphoma and extranodal diffuse large cell lymphoma are targeted by aberrant somatic hypermutation;Deutsch;Blood,2007

3. JE Comparison of epidemiological data on congenital hypothyroidism in Europe with those of other parts of world;Toublanc;Horm Res,1992

4. Molecular genetic defects in congenital hypothyroidism;Grüters;Eur J Endocrinol,2004

5. Mutation of the gene encoding human TTF associated with thyroid agenesis cleft palate and choanal atresia;Clifton;Nat Genet,1998

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