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Results: 5

1.

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.

Fukami M, Kirsch S, Schiller S, Richter A, Benes V, Franco B, Muroya K, Rao E, Merker S, Niesler B, Ballabio A, Ansorge W, Ogata T, Rappold GA.

Am J Hum Genet. 2000 Sep;67(3):563-73. Epub 2000 Jul 20.

PMID:
10903929
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosome.

Ballabio A, Bardoni B, Carrozzo R, Andria G, Bick D, Campbell L, Hamel B, Ferguson-Smith MA, Gimelli G, Fraccaro M, et al.

Proc Natl Acad Sci U S A. 1989 Dec;86(24):10001-5.

PMID:
2602357
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

An Xp22 microdeletion associated with ocular albinism and ichthyosis: approximation of breakpoints and estimation of deletion size by using cloned DNA probes and flow cytometry.

Schnur RE, Trask BJ, van den Engh G, Punnett HH, Kistenmacher M, Tomeo MA, Naids RE, Nussbaum RL.

Am J Hum Genet. 1989 Nov;45(5):706-20.

PMID:
2573275
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Long-range restriction map of the terminal part of the short arm of the human X chromosome.

Petit C, Levilliers J, Weissenbach J.

Proc Natl Acad Sci U S A. 1990 May;87(10):3680-4.

PMID:
2339111
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

X/Y translocations resulting from recombination between homologous sequences on Xp and Yq.

Yen PH, Tsai SP, Wenger SL, Steele MW, Mohandas TK, Shapiro LJ.

Proc Natl Acad Sci U S A. 1991 Oct 15;88(20):8944-8.

PMID:
1924355
[PubMed - indexed for MEDLINE]
Free PMC Article

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