Pure partial monosomy 3p (3p25.3 → pter): Prenatal diagnosis and array comparative genomic hybridization characterization
Author:
Funder
National Science Council
Mackay Memorial Hospital
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference22 articles.
1. Prenatal diagnosis of partial monosomy 3p and partial trisomy 2p in a fetus associated with shortening of long bones and a single umbilical artery;Chen;Prenat Diagn,1996
2. Distal 3p monosomy associated with epilepsy in a boy;Chen;Genet Counsel,2005
3. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy;Chen;Taiwan J Obstet Gynecol,2011
4. Microarray based analysis of 3p25-p26 deletions (3p- syndrome);Shuib;Am J Med Genet,2009
5. Detailed mapping of a congenital heart disease gene in chromosome 3p25;Green;J Med Genet,2000
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2. De novo 3p25-deletiós szindróma genotípus-fenotípus vizsgálata;Orvosi Hetilap;2022-03-20
3. Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy;Molecular Syndromology;2021
4. Fetal cystic hygroma associated with terminal 2p25.1 duplication and terminal 3p25.3 deletion: Cytogenetic, fluorescent in situ hybridization and microarray familial characterization of two different chromosomal structural rearrangements;Balkan Journal of Medical Genetics;2020-11-01
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