Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency-Reference-Cited by-同舟云学术

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Characterization of the deletion breakpoints in a patient with steroid sulfatase deficiency

Published:1994 Issue:1 Volume:4 Page:76-78
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Yen Pauline H.,Ferrero Giovanni B.,Chinault A. Craig,Mohandas Thuluvancheri,Ballabio Andrea

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference9 articles.

1. Construction and characterization of a yeast artificial chromosome library containing seven haploid human genome equivalents.

2. Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses

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

4. Sequence analysis of a partial deletion of the human steroid sulfatase gene reveals 3 bp of homology at deletion breakpoints

5. Systematic screening of yeast artificial-chromosome libraries by use of the polymerase chain reaction.

Cited by 3 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. Analysis of an interstitial deletion in a patient with Kallmann syndrome, X-linked ichthyosis and mental retardation;Clinical Genetics;2008-04-23

2. Deletion of Exons 1–5 of the STS Gene Causing X-Linked Ichthyosis;Journal of Investigative Dermatology;2001-03

3. X-linked ichthyosis: an update;British Journal of Dermatology;1999-10

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