A frequent oligogenic involvement in congenital hypothyroidism-Reference-Cited by-同舟云学术

A frequent oligogenic involvement in congenital hypothyroidism

Published:2017-04-21 Issue:13 Volume:26 Page:2507-2514
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

de Filippis Tiziana,Gelmini Giulia,Paraboschi Elvezia,Vigone Maria Cristina,Di Frenna Marianna,Marelli Federica,Bonomi Marco,Cassio Alessandra,Larizza Daniela,Moro Mirella,Radetti Giorgio,Salerno Mariacarolina,Ardissino Diego,Weber Giovanna,Gentilini Davide,Guizzardi Fabiana,Duga Stefano,Persani Luca

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/26/13/2507/17725804/ddx145.pdf

Reference40 articles.

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2. A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH);Clin. Endocrinol. (Oxf.),2009

3. Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism;Italian Study Group for Congenital Hypothyroidism;J. Clin. Endocrinol. Metab,2013

4. Congenital hypothyroidism: an evolving common clinical conundrum;J. Clin. Endocrinol. Metab,2010

5. Thyroid development and its disorders: genetics and molecular mechanisms;Endocr. Rev,2004

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