Prader-Willi Syndrome: Genetic Tests and Clinical Findings-Reference-Cited by-同舟云学术

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Prader-Willi Syndrome: Genetic Tests and Clinical Findings

Published:2000-12-19 Issue:4 Volume:4 Page:387-392
ISSN:1090-6576
Container-title:Genetic Testing
language:en
Short-container-title:Genetic Testing

Author:

Fridman Cintia¹,Varela Monica C.¹,Kok Fernando²,Setian Nuvarte³,Koiffmann Célia P.¹

Affiliation:

1. Department of Biology, Institute of Bioscience, University of São Paulo, São Paulo, Brazil.

2. Child Neurology Service, Department of Neurology, Hospital das Clínicas, School of Medicine, University of São Paulo, São Paulo, Brazil.

3. Pediatric Endocrinology Unit, Department of Pediatrics, Hospital das Clínicas, School of Medicine, University of São Paulo, São Paulo, Brazil.

Publisher

Mary Ann Liebert Inc

Subject

Genetics (clinical)

Link

http://www.liebertpub.com/doi/pdf/10.1089/109065700750065144

Reference34 articles.

1. Two cases of maternal uniparental disomy 14 with a phenotype overlapping with the Prader-Willi phenotype

2. Inherited microdeletions in the Angelman and Prader–Willi syndromes define an imprinting centre on human chromosome 15

3. Prader-Willi syndrome.

4. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15

Cited by 23 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. Premature adrenarche in Prader–Willi syndrome is associated with accelerated pre-pubertal growth and advanced bone age;Journal of Pediatric Endocrinology and Metabolism;2022-12-05

2. Genetic subtypes and phenotypic characteristics of 110 patients with Prader-Willi syndrome;Italian Journal of Pediatrics;2022-07-23

3. Prenatal diagnosis of a 15q11.2-q14 deletion of paternal origin associated with increased nuchal translucency, mosaicism for de novo multiple unbalanced translocations involving 15q11-q14, 5qter, 15qter, 17pter and 3qter and Prader–Willi syndrome;Taiwanese Journal of Obstetrics and Gynecology;2021-03

4. Comprehensive Orthodontic Treatment of a Patient With Prader–Willi Syndrome;The Cleft Palate-Craniofacial Journal;2020-12-04

5. Growth Friendly Surgery and Serial Cast Correction in the Treatment of Early-onset Scoliosis for Patients With Prader-Willi Syndrome;Journal of Pediatric Orthopaedics;2019-09

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