Targeted array comparative genomic hybridisation (array CGH) identifies genomic imbalances associated with isolated congenital diaphragmatic hernia (CDH)

Prenatal Diagnosis

Volumn 30, Issue 12-13, 2010, Pages 1198-1206

  Srisupundit, Kasemsri ^a,b,c   Brady, Paul D ^a   Devriendt, Koenraad ^a   Fryns, Jean Pierre ^a   Cruz Martinez, Rogelio ^d   Gratacos, Eduard ^d   Deprest, Jan A ^b   Vermeesch, Joris R ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

^b UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^c Faculty of Medicine Chiang Mai University   (Thailand)

^d UNIVERSITY OF BARCELONA   (Spain)

Author keywords

8p deletions; Array CGH; Congenital diaphragmatic hernia; EFNB1; Isolated CDH; Mosaic trisomy 2; Prenatal diagnosis

Indexed keywords

EPHRIN B1;

ARTICLE; CHROMOSOME 8P; CHROMOSOME DUPLICATION; CHROMOSOME XQ; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL DIAPHRAGM HERNIA; COPY NUMBER VARIATION; FETUS; GENE DELETION; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MOSAICISM; PRIORITY JOURNAL; TRISOMY; TRISOMY 2;

ALLELIC IMBALANCE; AMNIOTIC FLUID; CASE-CONTROL STUDIES; CELLS, CULTURED; CHROMOSOME ABERRATIONS; COMPARATIVE GENOMIC HYBRIDIZATION; FEMALE; HERNIA, DIAPHRAGMATIC; HUMANS; MALE; MASS SCREENING; PREGNANCY; PRENATAL DIAGNOSIS;

EID: 78649655581     PISSN: 01973851     EISSN: 10970223     Source Type: Journal    
DOI: 10.1002/pd.2651     Document Type: Article

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