Growth patterns of patients with 1p36 deletion syndrome-Reference-Cited by-同舟云学术

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Growth patterns of patients with 1p36 deletion syndrome

Published:2014-04-21 Issue:2 Volume:54 Page:82-86
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenital Anomalies

Author:

Sangu Noriko¹²,Shimojima Keiko²,Shimada Shino²³,Ando Tomohiro¹,Yamamoto Toshiyuki²

Affiliation:

1. Department of Oral and Maxillofacial Surgery; School of Medicine; Tokyo Women's Medical University; Tokyo Japan

2. Institute for Integrated Medical Sciences; Tokyo Women's Medical University; Tokyo Japan

3. Department of Pediatrics; Tokyo Women's Medical University; Tokyo Japan

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference13 articles.

1. Further delineation of deletion 1p36 syndrome in 60 patients: a recognizable phenotype and common cause of developmental delay and mental retardation;Battaglia;Pediatrics,2008

2. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems;D'Angelo;Eur J Med Genet,2006

3. Extending the phenotype of monosomy 1p36 syndrome and mapping of a critical region for obesity and hyperphagia;D'Angelo;Am J Med Genet A,2010

4. Monosomy 1p36 deletion syndrome;Gajecka;Am J Med Genet C Semin Med Genet,2007

5. Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome;Heilstedt;Am J Hum Genet,2003

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Syndromic and Nonsyndromic Obesity: Underlying Genetic Causes in Humans;Advanced Biology;2022-06-09

2. Monogenic and Syndromic Causes of Obesity;Management of Prader-Willi Syndrome;2022

3. First case of nonalcoholic steatohepatitis in a child with del(1p36) and dup (Xp22): review of the literature;Clinical Dysmorphology;2018-04

4. Short stature in genetic syndromes: Selected issues;Advances in Clinical and Experimental Medicine;2018-03-31

5. Identification of 1p36 deletion syndrome in patients with facial dysmorphism and developmental delay;Korean Journal of Pediatrics;2016

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