Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid Dysgenesis-Reference-Cited by-同舟云学术

Screening Chromosomal Aberrations by Array Comparative Genomic Hybridization in 80 Patients with Congenital Hypothyroidism and Thyroid Dysgenesis

Published:2010-07-01 Issue:7 Volume:95 Page:3446-3452
ISSN:0021-972X
Container-title:The Journal of Clinical Endocrinology & Metabolism
language:en
Short-container-title:

Author:

Thorwarth A.¹,Mueller I.²,Biebermann H.¹,Ropers H. H.²,Grueters A.¹,Krude H.¹,Ullmann R.²

Affiliation:

1. Institute for Experimental Pediatric Endocrinology (A.T., H.B., A.G., H.K.), Charite University Medicine, 13353 Berlin, Germany;

2. Max Planck Institute for Molecular Genetics (I.M., H.H.R., R.U.), 14195 Berlin, Germany

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Link

http://academic.oup.com/jcem/article-pdf/95/7/3446/9068928/jcem3446.pdf

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4. Long-term consequences of congenital hypothyroidism in the era of screening programmes.;Grüters;Best Pract Res Clin Endocrinol Metab,2002

5. Thyroid disorders;Vassart;In: Sciver CR, Beaudet AL, Sly WS, Valle D, eds. The metabolic and molecular basis of inherited disease. New York: McGraw Hill, Inc.;,1995

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