Renal complications in 6p duplication syndrome: Microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)-Reference-Cited by-同舟云学术

Renal complications in 6p duplication syndrome: Microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS)

Published:2015-02-18 Issue:3 Volume:167 Page:592-601
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Yoshimura-Furuhata Megumi¹²,Nishimura-Tadaki Akira³,Amano Yoshiro¹,Ehara Takashi⁴,Hamasaki Yuko⁵,Muramatsu Masaki⁶,Shishido Seiichiro⁵,Aikawa Atsushi⁶,Hamada Riku⁷,Ishikura Kenji⁷,Hataya Hiroshi⁷,Hidaka Yoshihiko²,Noda Shunsuke²,Koike Kenichi²,Wakui Keiko⁸,Fukushima Yoshimitsu⁸,Matsumoto Naomichi³,Awazu Midori⁹,Miyake Noriko³,Kosho Tomoki⁸

Affiliation:

1. Department of Pediatrics; Nagano Red Cross Hospital; Nagano Japan

2. Department of Pediatrics; Shinshu University School of Medicine; Matsumoto Japan

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

4. Department of Health and Sport Science; Graduate School of Health Sciences; Matsumoto University; Matsumoto Japan

5. Department of Pediatric Nephrology; School of Medicine; Toho University; Tokyo Japan

6. Department of Nephrology; School of Medicine; Toho University; Tokyo Japan

7. Department of Nephrology; Tokyo Metropolitan Children's Medical Center; Fuchu Japan

8. Department of Medical Genetics; Shinshu University School of Medicine; Matsumoto Japan

9. Department of Pediatrics; School of Medicine; Keio University; Tokyo Japan

Funder

Research on Intractable Diseases, Ministry of Health, Labour and Welfare, Japan

The Strategic Research Program for Brain Sciences

Ministry of Education, Culture, Sports, Science and Technology of Japan

A Grant-in-Aid for Scientific Research from Japan Society for the Promotion of Science

The Takeda Science Foundation

The Hayashi Memorial Foundation for Female Natural Scientists

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference39 articles.

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4. Familial translocation t(6;20)(p21;p13) resulting in partial trisomy 6p and partial monosomy 20p: Report of a new case and review of the literature;Berner;Cytogenet Genome Res,2012

5. Partial trisomy 6p;Bernheim;Hum Genet,1979

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