A Search for the Possible Molecular Mechanisms of Thyroid Dysgenesis: Sex Ratios and Associated Malformations
Author:
Affiliation:
1. McGill University (C.R.), H3T 1C5 Canada
2. University of Sherbrooke (N.G.), H3T 1C5 Canada
3. Laval University (R.L.), Montreal, Quebec, H3T 1C5 Canada
4. Departments of Pediatrics, University of Montreal (G.V.V), H3T 1C5 Canada
Publisher
The Endocrine Society
Subject
Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism
Link
http://academic.oup.com/jcem/article-pdf/84/7/2502/9215847/jcem2502.pdf
Reference45 articles.
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2. Congenital anomalies concomitant with persistent primary congenital hypothyroidism.;Siebner;Am J Med Genet,1992
3. Population study of congenital hypothyroidism and associated birth defects, Atlanta, 1979–1992.;Roberts;Am J Med Genet,1997
4. Increased incidence of congenital malformations in children with transient thyroid-stimulating hormone elevation on neonatal screening.;Oakley;J Pediatr,1998
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