Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

Journal of Medical Genetics

Volumn 47, Issue 9, 2010, Pages 586-594

  Faas, Brigitte H W ^a   Van Der Burgt, I ^a   Kooper, A J A ^a   Pfundt, R ^a   Hehir Kwa, J Y ^a   Smits, A P T ^a   De Leeuw, N ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME ABERRATION; CHROMOSOME IDENTIFICATION; CLINICAL ARTICLE; CONTROLLED STUDY; DNA ISOLATION; FETUS; FETUS DEATH; FETUS ECHOGRAPHY; FETUS MALFORMATION; HUMAN; KARYOTYPE; MICROARRAY ANALYSIS; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; UNIPARENTAL DISOMY;

BASE PAIRING; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN; DNA COPY NUMBER VARIATIONS; FEMALE; FETUS; GENOME, HUMAN; HOMOZYGOTE; HUMANS; INFANT, NEWBORN; OLIGONUCLEOTIDE ARRAY SEQUENCE ANALYSIS; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; ULTRASONOGRAPHY, PRENATAL; UNIPARENTAL DISOMY;

EID: 77956117452     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2009.075853     Document Type: Article

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