A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay-Reference-Cited by-同舟云学术

A de novo 1.4-Mb deletion at 21q22.11 in a boy with developmental delay

Author:

Fukai Ryoko¹²,Hiraki Yoko³,Nishimura Gen⁴,Nakashima Mitsuko¹,Tsurusaki Yoshinori¹,Saitsu Hirotomo¹,Matsumoto Naomichi¹,Miyake Noriko¹

Affiliation:

1. Department of Human Genetics; Yokohama City University Graduate School of Medicine; Yokohama Japan

2. Department of Neurology and Stroke Medicine; Yokohama City University Graduate School of Medicine; Yokohama Japan

3. Hiroshima Municipal Center for Child Health and Development; Hiroshima Japan

4. Department of Pediatric Imaging; Tokyo Metropolitan Children's Medical Center; Fuchu Tokyo Japan

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference36 articles.

4. Braddock SR Schiffman JD Sarah T South ST Carey JC 2011 Braddock-Carey syndrome: A twenty year journey ends with a new microdeletion syndrome

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4. A CNV Catalogue;Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017