Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma.

doi:10.1016/j.tjog.2014.12.003

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Article

Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma.

Taiwanese journal of obstetrics & gynecology - 1 Feb 2015

Chen Chih-Ping, Ko Tsang-Ming, Huang Ming-Chao, Chern Schu-Rern, Lin Tan-Wei, Chang Tung-Yao, Kuo Yu-Ling, Chen Wen-Lin, Wang Wayseen

Abstract excerpt

No abstract is available from the source.

Topics

Adult
Alleles
Chromosome Disorders
Chromosomes, Human, Pair 13
Female
Fetal Diseases
Humans
Isochromosomes
Karyotyping
Male
Microsatellite Repeats
Pedigree
Pregnancy
Prenatal Diagnosis
Trisomy
Trisomy 13 Syndrome

Source

Open in PubMed

Identifiers

PMID: 25675926
DOI: 10.1016/j.tjog.2014.12.003

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