Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion-Reference-Cited by-同舟云学术

Fifty microdeletions among 112 cases of Sotos syndrome: Low copy repeats possibly mediate the common deletion

Published:2003-09-24 Issue:5 Volume:22 Page:378-387
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Kurotaki Naohiro,Harada Naoki,Shimokawa Osamu,Miyake Noriko,Kawame Hiroshi,Uetake Kimiaki,Makita Yoshio,Kondoh Tatsuro,Ogata Tsutomu,Hasegawa Tomoko,Nagai Toshiro,Ozaki Takao,Touyama Mayumi,Shenhav Ruthie,Ohashi Hirofumi,Medne Livija,Shiihara Takashi,Ohtsu Shigeyuki,Kato Zen-ichiro,Okamoto Nobuhiko,Nishimoto Junji,Lev Dorit,Miyoshi Yoko,Ishikiriyama Satoshi,Sonoda Tohru,Sakazume Satoru,Fukushima Yoshimitsu,Kurosawa Kenji,Cheng Jan-Fang,Yoshiura Koh-ichiro,Ohta Tohru,Kishino Tatsuya,Niikawa Norio,Matsumoto Naomichi

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference23 articles.

1. Growth in Sotos syndrome

2. Sotos syndrome: a study of the diagnostic criteria and natural history.

3. NSD1 Mutations Are the Major Cause of Sotos Syndrome and Occur in Some Cases of Weaver Syndrome but Are Rare in Other Overgrowth Phenotypes

4. Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas

5. Familial Sotos syndrome is caused by a novel 1 bp deletion of the NSD1 gene

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