Molecular Studies of a Patient with Complete Androgen Insensitivity and a 47,XXY Karyotype-Reference-Cited by-同舟云学术

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Molecular Studies of a Patient with Complete Androgen Insensitivity and a 47,XXY Karyotype

Published:2009-09 Issue:3 Volume:155 Page:439-443
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Girardin C.M.,Deal C.,Lemyre E.,Paquette J.,Lumbroso R.,Beitel L.K.,Trifiro M.A.,Van Vliet G.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference21 articles.

1. Disorders of sex development;Acherman,2008

2. Klinefelter's syndrome;Lanfranco;Lancet,2004

3. CDC growth charts: United States;Kuczmarski;Adv Data,2000

4. The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence;Wilkins,1965

5. Radiographic Atlas of Skeletal Development of the Hand and Wrist;Greulich,1959

Cited by 13 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. Prevalence of sex‐chromosome aneuploidy estimated using SNP genotype intensity information in a large population of juvenile dairy and beef cattle;Journal of Animal Breeding and Genetics;2024-03-29

2. 18-Year-old patient with Klinefelter syndrome (47, XXY) and complete androgen insensitivity syndrome (CAIS) – case report;Gynecological Endocrinology;2021-05-07

3. Oligogenic Origin of Differences of Sex Development in Humans;International Journal of Molecular Sciences;2020-03-06

4. A 47,XXY Pregnant Woman without the SRY Gene;Sexual Development;2019

5. Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings;Journal of Clinical Research in Pediatric Endocrinology;2018-05-18

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