The genotype and phenotype of chromosome 18p deletion syndrome-Reference-Cited by-同舟云学术

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The genotype and phenotype of chromosome 18p deletion syndrome

Published:2021-05-07 Issue:18 Volume:100 Page:e25777
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Jin Qiujie,Qiang Rong,Cai Bo,Wang Xiaobin,Cai Na,Zhen Shuai,Zhai Wen

Funder

Special Talent Training Program in Northwest Women's and Children's Hospital

Fundamental Research Funds for the Central Universities

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference26 articles.

1. 18p-syndrome: presentation of two cases with alobar holoprosencenphaly;Pachajoa;Colomb Med,2010

2. Monosomy 18p;Turleau;Orphanet J Rare Dis,2008

3. Clinical and molecular characterization of individuals with 18p deletion: a genotype-phenotype correlation;Wester;Am J Med Genet A,2006

4. A 13-year-old girl with 18p deletion syndrome presenting turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows;Chen;Taiwan J Obstet Gynecol,2018

5. Prenatal diagnosis of monosomy 18p associated with holoprosencephaly: case report;Yin;J Obstet Gynaecol,2017

Cited by 10 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. Congenital Anomalies;Ocular Pathology;2025

2. Prenatal detection of distal 18p deletion by chromosomal microarray analysis: Three case reports and literature review;Medicine;2024-07-26

3. Prenatal diagnosis of dicentric chromosome X mosaicism: a case report and review;Frontiers in Genetics;2024-07-18

4. Cytogenomic characterization of small supernumerary marker chromosomes in patients with pigmentary mosaicism;Frontiers in Genetics;2024-04-16

5. Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case;BMC Women's Health;2024-04-15

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