Duplication of 8p23.2: A benign cytogenetic variant?-Reference-Cited by-同舟云学术

Duplication of 8p23.2: A benign cytogenetic variant?

Published:2002-07-29 Issue:3 Volume:111 Page:285-288
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Harada Naoki,Takano Jun,Kondoh Tatsuro,Ohashi Hirofumi,Hasegawa Tomonobu,Sugawara Hirobumi,Ida Tomoko,Yoshiura Ko-ichiro,Ohta Tohru,Kishino Tatsuya,Kajii Tadashi,Niikawa Norio,Matsumoto Naomichi

Publisher

Wiley

Subject

Genetics (clinical)

Reference10 articles.

1. Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.

2. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL

3. Familial partial trisomy 8p without dysmorphic features and only mild mental retardation

4. Duplication of chromosome region 8p23.1 ? p23.3: A benign variant?

5. Direct duplication of 8p21.3?p23.1: A cytogenetic anomaly associated with developmental delay without consistent clinical features

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