Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type-Reference-Cited by-同舟云学术

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Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type

Published:1991-12 Issue:2 Volume:88 Page:162-166
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Bergen A. A. B.,Samanns C.,Schuurman E. J. M.,van Osch L.,van Dorp D. B.,Pinckers A. J. L. G.,Bakker E.,Gal A.,van Ommen G. J. B.,Bleeker-Wagemakers E. M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00206065.pdf

Cited by 43 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Deep intronic GPR143 mutation in a Japanese family with ocular albinism;Scientific Reports;2015-06-10

2. Diagnosis of idiopathic infantile nystagmus and ocular albinism: a clinical challenge;Expert Review of Ophthalmology;2009-08

3. DNA carrier detection in X-linked progressive cone dystrophy;Clinical Genetics;2008-06-28

4. Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis;Clinical Genetics;2008-06-28

5. Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotides;Human Mutation;2006

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