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Clinical practice in Turner syndrome

Published:2005-11 Issue:1 Volume:1 Page:41-52
ISSN:1745-8366
Container-title:Nature Clinical Practice Endocrinology & Metabolism
language:en
Short-container-title:Nat Rev Endocrinol

Author:

Gravholt Claus H

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

http://www.nature.com/articles/ncpendmet0024.pdf

Reference80 articles.

1. Ogata T et al. (1995) Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features. Hum Genet 95: 607–629

2. Gravholt CH et al. (1996) Prenatal and postnatal prevalence of Turner's syndrome: a registry study. BMJ 312: 16–21

3. Ellison JW et al. (1997) PHOG, a candidate gene for involvement in the short stature of Turner syndrome. Hum Mol Genet 6: 1341–1347

4. Rao E et al. (1997) Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome. Nat Genet 16: 54–63

5. Hook EB et al. (1983) The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism. Hum Genet 64: 24–27

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