Inherited duplication Xq27-qter at Xp22.3 in severely affected males: Molecular cytogenetic evaluation and clinical description in three unrelated families-Reference-Cited by-同舟云学术

Inherited duplication Xq27-qter at Xp22.3 in severely affected males: Molecular cytogenetic evaluation and clinical description in three unrelated families

Published:1998-12-04 Issue:4 Volume:80 Page:377-384
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Goodman Barbara K.,Shaffer Lisa G.,Rutberg Julie,Leppert Mary,Harum Karen,Gagos Sarantis,Ray James H.,Bialer Martin G.,Zhou Xianting,Pletcher Beth A.,Shapira Stuart K.,Geraghty Michael T.

Publisher

Wiley

Subject

Genetics(clinical)

Reference33 articles.

1. Two families of low-copy-number repeats are interspersed on Xp22.3: Implications for the high frequency of deletions in this region

2. Detection of a subtle rearrangement of chromosome 22 using molecular techniques

3. Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17

4. Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci

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