Human microphthalmia associated with mutations in the retinal homeobox gene CHX10-Reference-Cited by-同舟云学术

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

Published:2000-08 Issue:4 Volume:25 Page:397-401
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Ferda Percin E.,Ploder Lynda A.,Yu Jessica J.,Arici Kemal,Jonathan Horsford D.,Rutherford Adam,Bapat Bharati,Cox Diane W.,Duncan Alessandra M.V.,Kalnins Vitauts I.,Kocak-Altintas Aysegul,Sowden Jane C.,Traboulsi Elias,Sarfarazi Mansoor,McInnes Roderick R.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0800_397.pdf

Reference28 articles.

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2. Othman, M.I. et al. Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11. Am. J. Hum. Genet. 63, 1411–1418 (1998).

3. Bessant, D.A. et al. A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. Am. J. Hum. Genet. 62, 1113–1116 (1998).

4. Al-Gazali, L.I. et al. Two 46,XX,t(X;Y) females with linear skin defects and congenital microphthalmia: a new syndrome at Xp22.3. J. Med. Genet. 27, 59–63 (1990).

5. Yokoyama, Y., Narahara, K., Tsuji, K., Ninomiya, S. & Senio, Y. Autosomal dominant congenital cataract and microphthalmia associated with a familial t(2;16) translocation. Hum. Genet. 90, 177–178 (1992).

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