Array-based approaches in prenatal diagnosis

Methods in Molecular Biology

Volumn 838, Issue , 2012, Pages 151-171

  Brady, Paul D ^a   Devriendt, Koenraad ^a   Deprest, Jan ^b   Vermeesch, Joris R ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

Author keywords

Array CGH; CNV; Copy number variation; Incidental findings; Miscarriage; PGD; POC; Prenatal diagnosis; Unclassified variants

Indexed keywords

ARTICLE; CHROMOSOME ABERRATION; COMPARATIVE GENOMIC HYBRIDIZATION; COPY NUMBER VARIATION; DNA MICROARRAY; FEMALE; GENETIC POLYMORPHISM; GENETICS; HUMAN; INTELLECTUAL IMPAIRMENT; KARYOTYPING; MALE; METHODOLOGY; MULTIPLE MALFORMATION SYNDROME; PREGNANCY; PRENATAL DIAGNOSIS; SPONTANEOUS ABORTION;

ABNORMALITIES, MULTIPLE; ABORTION, SPONTANEOUS; CHROMOSOME ABERRATIONS; COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; FEMALE; HUMANS; INTELLECTUAL DISABILITY; KARYOTYPING; MALE; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, GENETIC; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84856244930     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-61779-507-7_7     Document Type: Article

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