The introduction of arrays in prenatal diagnosis: A special challenge

Human Mutation

Volumn 33, Issue 6, 2012, Pages 923-929

  Vetro, Annalisa ^a   Bouman, Katelijne ^b   Hastings, Ros ^c   McMullan, Dominic J ^d   Vermeesch, Joris R ^e   Miller, Konstantin ^f   Sikkema Raddatz, Birgit ^b   Ledbetter, David H ^g   Zuffardi, Orsetta ^a,h   van Ravenswaaij Arts, Conny M A ^a,b  

^a UNIVERSITY OF PAVIA   (Italy)

^b UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^c JOHN RADCLIFFE HOSPITAL   (United Kingdom)

^d BIRMINGHAM CHILDREN S HOSPITAL NHS FOUNDATION TRUST   (United Kingdom)

^e UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^f HANNOVER MEDICAL SCHOOL   (Germany)

^g GEISINGER HEALTH SYSTEM   (United States)

^h C MONDINO NATIONAL NEUROLOGICAL INSTITUTE   (Italy)

Author keywords

Genome wide array analysis; Guidelines; Prenatal diagnosis

Indexed keywords

OLIGONUCLEOTIDE;

ANEUPLOIDY; ARTICLE; CLINICAL PROTOCOL; COMPARATIVE GENOMIC HYBRIDIZATION; CONSENSUS DEVELOPMENT; CONTROLLED STUDY; COPY NUMBER VARIATION; CYTOGENETICS; DNA MICROARRAY; DOWN SYNDROME; FETUS; FETUS MALFORMATION; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC COUNSELING; HISTOPATHOLOGY; HUMAN; KARYOTYPING; LABORATORY TEST; METAPHASE; MICROARRAY ANALYSIS; MONOSOMY X; MOSAICISM; MULTIPLEX LIGATION DEPENDENT PROBE AMPLIFICATION; PATHOLOGIST; PHYSICIAN; POLYMERASE CHAIN REACTION; PRACTICE GUIDELINE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK FACTOR; SCREENING TEST; SINGLE NUCLEOTIDE POLYMORPHISM;

COMPARATIVE GENOMIC HYBRIDIZATION; DNA COPY NUMBER VARIATIONS; FEMALE; GENETIC COUNSELING; GUIDELINES AS TOPIC; HUMANS; INFORMED CONSENT; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 84865195385     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.22050     Document Type: Article

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