Clinical practice in Turner syndrome
Author:
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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