Ophthalmic features of Turner's syndrome

Author:

Denniston A K O,Butler L

Publisher

Springer Science and Business Media LLC

Subject

Ophthalmology

Reference39 articles.

1. Hsu LYF . Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In: Mulinsky A (ed). Genetic Disorders and the Fetus. Johns Hopkins University Press: Baltimore, MD, 1998, pp 179–248.

2. Turner HH . A syndrome of infantilism, congenital webbed neck and cubitus valgus. Endocrinology 1938; 23: 566–574.

3. Moore KL The Sex Chromatin. WB Saunders: Philadelphia, PA, 1966.

4. Mathur A, Stekol L, Schatz D, MacLaren NK, Scott ML, Lippe B . The parental origin of the single X chromosome in Turner syndrome: lack of correlation with parental age or clinical phenotype. Am J Hum Genet 1991; 48: 682–686.

5. Rao E, Weiss B, Fukami M et al. Pseudoautosomal deletions encompassing a novel homeobox gene causing growth failure in idiopathic short stature and Turner syndrome. Nat Genet 1997; 16: 54–63.

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