Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations
Author:
Funder
National Science and Technology Council
Publisher
Elsevier BV
Reference23 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. Partial monosomy 3p (3p26.2→pter) and partial trisomy 5q (5q34→qter) in a girl with coarctation of the aorta, congenital heart defects, short stature, microcephaly and developmental delay;Chen;Genet Counsel,2012
3. Pure partial monosomy 3p (3p25.3→pter): prenatal diagnosis and array comparative genomic hybridization characterization;Chen;Taiwan J Obstet Gynecol,2012
4. Prenatal diagnosis of distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization;Chen;Taiwan J Obstet Gynecol,2013
5. Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter);Chen;Taiwan J Obstet Gynecol,2016
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