Speech and language development in children with 49, XXXXY syndrome-Reference-Cited by-同舟云学术

Speech and language development in children with 49, XXXXY syndrome

Published:2020-07-28 Issue:12 Volume:185 Page:3567-3575
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Samango‐Sprouse Carole A.¹²³^ORCID,Lasutschinkow Patricia C.³,McLeod Michael³,Porter Grace F.³,Powell Sherida⁴,St. Laurent Jillyan³,Sadeghin Teresa³,Gropman Andrea L.⁵⁶

Affiliation:

1. Department of Pediatrics George Washington University Washington District of Columbia USA

2. Department of Human and Molecular Genetics Florida International University Miami Florida USA

3. The Focus Foundation Davidsonville Maryland USA

4. Department of Economics George Washington University Washington District of Columbia USA

5. Division of Neurogenetics and Developments Pediatrics Children's National Health System Washington District of Columbia USA

6. Department of Neurology George Washington University Washington District of Columbia USA

Funder

Fundación Focus

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.61767

Reference32 articles.

1. American Speech‐Language‐Hearing Association. (2007).Childhood apraxia of speech[Position statement]. Retrieved fromwww.asha.org/policy/

2. The 49,XXXXY syndrome. Clinical and psychological follow-up data

Cited by 7 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. Genetic outcomes in children with developmental language disorder: a systematic review;Frontiers in Pediatrics;2024-01-17

2. Update on Identification and Treatment of Infants and Toddlers With Suspected Childhood Apraxia of Speech;Journal of Speech, Language, and Hearing Research;2023-07-13

3. The Effect of Hormonal Therapy on the Behavioral Outcomes in 47,XXY (Klinefelter Syndrome) between 7 and 12 Years of Age;Genes;2023-07-06

4. The behavioral profile of 49,XXXXY and the potential impact of testosterone replacement therapy;Genetics in Medicine;2023-07

5. Short stature, cubitus varus, foot deformity and intellectual disability with sexual infantilism: clinical clues to 49,XXXXY variant of Klinefelter syndrome;BMJ Case Reports;2023-01