Prenatal diagnosis of 22q11 microdeletion

Prenatal Diagnosis

Volumn 17, Issue 11, 1997, Pages 1033-1037

  Levy Mozziconacci, Annie ^a   Piquet, Caroline ^a   Heurtevin, Pierre Christophe ^a   Philip, Nicole ^a  

^a TIMONE HOSPITAL   (France)

Author keywords

22q11 deletion; Congenital heart defects; DiGeorge syndrome; Prenatal diagnosis

Indexed keywords

AMNION CELL; ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CLINICAL ARTICLE; DIGEORGE SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PREGNANCY; PRENATAL DIAGNOSIS; ULTRASONOGRAPHY, PRENATAL;

EID: 0030669175     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-0223(199711)17:11<1033::AID-PD190>3.0.CO;2-2     Document Type: Article

References (24)

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