Genetic effects of a 13q31.1 microdeletion detected by noninvasive prenatal testing (NIPT)

Microdeletions of chromosome 13q31.1 are relatively rare. These types of deletions may cause different genetic effects on genotypes and/or phenotypes. There are several ways to detect microdeletions; noninvasive prenatal testing (NIPT) is the newest detection method. In this study, we aimed to inves...

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Veröffentlicht in:	International journal of clinical and experimental pathology 2014-01, Vol.7 (10), p.7003-7011
Hauptverfasser:	Jia, Yifang, Zhao, Heyong, Shi, Donghong, Peng, Wen, Xie, Luwen, Wang, Wei, Jiang, Fuman, Zhang, Hongyun, Wang, Xietong
Format:	Artikel
Sprache:	eng
Schlagworte:	Amniotic Fluid - chemistry Case Report Chromosome Deletion Chromosome Disorders - blood Chromosome Disorders - diagnosis Chromosome Disorders - genetics Chromosomes, Human, Pair 13 Comparative Genomic Hybridization Female Genetic Counseling Genetic Testing Humans Karyotype Live Birth Phenotype Predictive Value of Tests Pregnancy Prenatal Diagnosis - methods Reproducibility of Results
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