Possible role of imprinting in the Turner phenotype.

Author:

Chu C E,Donaldson M D,Kelnar C J,Smail P J,Greene S A,Paterson W F,Connor J M

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference10 articles.

1. A cytogenetic and molecular reappraisal of a series of patients with Turner's syndrome;Jacobs, P.A.; Betts, P.R.; Cockwell, A.E.;Ann Hum Genet,1990

2. Cytogenetic and molecular analysis of sex-chromosome monosomy;Hassold, T.; Benham, F.; Leppert, M.;Am7Hum Genet,1988

3. Molecular study of 45, X conceptuses; correlation with clinical findings. Am J';Lorda-Sanchez, I.; Binkert, F.; Maechler, M.; Schinzel, A.;Med Genet,1992

4. The parental origin of the single X chromosome in Turner's syndrome: lack of correlation with parental age or clinical phenotype;Mathur, A.; Stekol, L.; Schatz, D.; MacLaren, N.K.; Scott, M.L.; Lippe, B.;Am Hum Genet,1991

5. Pfender EG. The contribution of imprinting of the phenotype in Turner syndrome;Ross, J.L.; Hall, J.G.;Am Hum Genet; Growth in children with 45, XO Turner's syndrome,1991

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