Partial trisomy 9: prenatal diagnosis and recurrence within same family-Reference-Cited by-同舟云学术

Partial trisomy 9: prenatal diagnosis and recurrence within same family

Published:2017-05-10 Issue:6 Volume:5 Page:986-992
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

López-Félix Jana¹^ORCID,Flores-Gallegos Leticia¹,Garduño-Zarazúa Luz²,Leis-Márquez Teresa¹,Juárez-García Luz¹,Meléndez-Hernández Ricardo²,Castelazo-Morales Ernesto³,Mayén-Molina Dora²

Affiliation:

1. Clínica Materno-Fetal; Hospital Angeles Lomas; Huixquilucan México

2. Genetics Clinic; Hospital Angeles Lomas; Huixquilucan México

3. Centro Especializado para la Atención de la Mujer; Hospital Angeles Lomas; Huixquilucan Mexico

Publisher

Wiley

Subject

General Medicine

Reference29 articles.

1. A case of trisomy 9;Feingold;J. Med. Genet.,1973

2. Trisomy 9: predominance of cardiovascular, liver, brain, and skeletal anomalies in the first diagnosed case;Kurnick;Hum. Pathol.,1974

3. Trisomy 9: review and report of two new cases;Arnold;Am. J. Med. Genet.,1995

4. Mosaic vs non mosaic trisomy 9: report of a liveborn infant evaluated by fluorescence in situ hybridization and review of the literature;Cantú;Am. J. Med. Genet.,1996

Cited by 5 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. Case report: Detection of fetal trisomy 9 mosaicism by multiple genetic testing methods: Report of two cases;Frontiers in Genetics;2023-03-10

2. A rare case of partial trisomy 9q with dysmorphic clinical features and Hirschsprung's disease;INT J PEDIATR-MASSHA;2022

3. Perinatal outcomes of prenatal cases testing positive for trisomy 9 by noninvasive prenatal testing;Taiwanese Journal of Obstetrics and Gynecology;2022-11

4. AN UNBALANCED PRODUCT DUE TO A MATERNAL RECIPROKAL ADJACENT-2 SEGREGATION CASE WITH DICENTRIC PARTIAL TRISOMY 9;Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi;2022-03-11

5. Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter>14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features;Intractable & Rare Diseases Research;2019-02-28