Morphological abnormalities in children with thyroidal congenital hypothyroidism

Author:

Kempers Marlies J.E.,Ozgen Heval M.,Vulsma Thomas,Merks Johannes H.,Zwinderman Koos H.,de Vijlder Jan J.M.,Hennekam Raoul C.M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference48 articles.

1. Congenital anomalies in infants with congenital hypothyroidism: Is it a coincidental or an associated finding?;Al Jurayyan;Hum Hered,1997

2. Congenital anomalies associated with hypothyroidism;Bamforth;Arch Dis Child,1986

3. Controlling the false discovery rate: A practical and powerful approach to multiple testing;Benjamini;J R Stat Soc Ser B,1995

4. Mutations of the human thyrotropin receptor gene causing thyroid hypoplasia and persistent congenital hypothyroidism;Biebermann;J Clin Endocrinol Metab,1997

5. Nineteen years of national screening for congenital hypothyroidism: Familial cases with thyroid dysgenesis suggest the involvement of genetic factors;Castanet;J Clin Endocrinol Metab,2001

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