Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum-Reference-Cited by-同舟云学术

Clinical report of 8 patients with 49,XXXXY syndrome: Delineation of the facial gestalt and depiction of the clinical spectrum

Published:2019-03 Issue:3 Volume:62 Page:210-216
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Burgemeister Anna L.,Daumiller Eva,du Bois Gabriele,Graul-Neumann Luitgard M.,Köhler Birgit,Knecht Susanne,Burgemeister Stefan,Gronwald Sarah,Maurer Martin H.^ORCID,Zirn Birgit

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference20 articles.

1. Brain morphological abnormalities in 49,XXXXY syndrome: a pediatric magnetic resonance imaging study;Blumenthal;Neuroimage Clin,2013

2. Neue Wachstumskurven für die Schweiz.Paediatrica;Braegger;Bull. Soc. Suisse Pediatr.,2011

3. Neurocognitive variance and neurological underpinnings of the X and Y chromosomal variations;Gropman;Am. J. Med. Genet. C,2013

4. Clinical variability and novel neurodevelopmental findings in 49,XXXXY syndrome;Gropman;Am. J. Med. Genet.,2010

5. Brain magnetic imaging findings in 49,XXXXY syndrome;Hoffman;Pediatr. Neurol.,2008

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. The timely diagnosis of 49, XXXXY with the combined detection of MLPA, karyotype, and QF-PCR in a newborn with multiple congenital malformations: a case report;Translational Pediatrics;2023-02

2. Clinical, Cognitive and Neurodevelopmental Profile in Tetrasomies and Pentasomies: A Systematic Review;Children;2022-11-09

3. 49, XXXXY syndrome: A case study and a systematic review of clinical features among the Iranian population;Clinical Case Reports;2022-09

4. Congenital Radioulnar Synostosis;Congenital Anomalies of the Upper Extremity;2021

5. Speech and language development in children with 49, XXXXY syndrome;American Journal of Medical Genetics Part A;2020-07-28