Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene-Reference-Cited by-同舟云学术

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Prenatal detection of terminal 9p24.3 microduplication encompassing DOCK8 gene

Published:2021-01-22 Issue:3 Volume:100 Page:e23967
ISSN:0025-7974
Container-title:Medicine
language:en
Short-container-title:

Author:

Yue Fagui,Yu Yang,Zhang Xinyue,Jiang Yuting,Li Leilei,Liu Ruizhi,Zhang Hongguo

Funder

the 10th Youth Foundation of the First Hospital of Jilin University

the Finance Department Health Special Project of Jilin Province, China.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference27 articles.

1. 4 cases of trisomy for the short arm of chromosome 9. Individualization of a new morbid entity;Rethoré;Ann Genet,1970

2. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up;Littooij;Am J Med Genet,2002

3. Prenatal diagnosis of maternal partial trisomy 9p23p24.3 and 14q11 2q21 3 in a fetus: A case report;Wu;Mol Cytogenet,2020

4. Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization;Jelin;J Craniofac Surg,2010

5. The phenotypic and cytogenetic spectrum of partial trisomy 9;Wilson;Am J Med Genet,1985

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