Polyhydramnios as a prenatal symptom of the DiGeorge/velo-cardio-facial syndrome

Prenatal Diagnosis

Volumn 18, Issue 1, 1998, Pages 68-72

  Devriendt, Koenraad ^a,b   Van Schoubroeck, Dominique ^a   Eyskens, Benedicte ^a   Vantrappen, Greet ^a   Swillen, Ann ^a   Gewillig, Marc ^a   Dumoulin, Monique ^a   Moerman, Philippe ^a   Vandenberghe, Kamiel ^a   Fryns, Jean Pierre ^a  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b CENTER FOR HUMAN GENETICS   (Belgium)

Author keywords

Deletion 22q11; DiGeorge syndrome; Polyhydramnios; Velo cardio facial syndrome

Indexed keywords

AMNIOCENTESIS; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; FEMALE; FETUS; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HYDRAMNIOS; HYDRONEPHROSIS; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

AMNIOCENTESIS; CHROMOSOMES, HUMAN, PAIR 22; CRANIOFACIAL ABNORMALITIES; FATAL OUTCOME; FEMALE; GENE DELETION; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT, NEWBORN; KARYOTYPING; POLYHYDRAMNIOS; PREGNANCY; PRENATAL DIAGNOSIS; SYNDROME; TETRALOGY OF FALLOT; TRUNCUS ARTERIOSUS, PERSISTENT; ULTRASONOGRAPHY, PRENATAL;

EID: 0031984325     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199801)18:1<68::AID-PD211>3.0.CO;2-I     Document Type: Article

References (25)

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