Prenatal diagnosis of complete sole trisomy 1q
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference20 articles.
1. Chromosome imbalance, normal phenotype, and imprinting.
2. Confirmation of proximal 1q duplication using fluorescence in situ hybridization
3. Mosaicism for a tandem duplication dup(1)(q12q22) in an 18 year old female.
Cited by 21 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 counseling of mosaicism for a duplication due to partial trisomy in a cell line with 46 chromosomes associated with a normal cell line at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2024-09
2. Chromosomal abnormalities associated with fetal pleural effusion (II): Specific and non-specific chromosome aberrations;Taiwanese Journal of Obstetrics and Gynecology;2024-03
3. Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype;Prenatal Diagnosis;2017-05-23
4. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: Molecular cytogenetic analysis, fetal pathology and review of the literature;Birth Defects Research Part A: Clinical and Molecular Teratology;2014-02-12
5. Monosomy 3pter-p25.3 and Trisomy 1q42.13-qter in a Boy With Profound Growth and Developmental Restriction, Multiple Congenital Anomalies, and Early Death;Pediatrics & Neonatology;2013-06
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