Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybrids-Reference-Cited by-同舟云学术

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Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybrids

Published:1997 Issue:3-4 Volume:76 Page:223-228
ISSN:1424-859X
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Cell Genet

Author:

Boycott K.M.,Moore B.J.,Gratton K.J.,Stoddart K.L.,Roland B.,Bech-Hansen N.T.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 7 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. A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants;Human Genetics;2001-03-01

2. An autopsy case of Klinefelter’s syndrome suspected and its DNA analysis;Forensic Science International;2000-09

3. Development of a 1.4-Mb BAC/PAC Contig and Physical Map within the Critical Region for Complete X-Linked Congenital Stationary Night Blindness in Xp11.4;Genomics;2000-08

4. Physical map covering a 2Mb region in human Xp11.3 distal to DX6849;Gene;1999-02

5. Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness;Nature Genetics;1998-07

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