Chromosome 22q11 deletions in patients with selected outflow tract malformations

Genetic Counseling

Volumn 10, Issue 1, 1999, Pages 35-41

  Frohn Mulder, I M E ^a   Swaay, E Wesby V ^b   Bouwhuis, C ^b   Van Hemel, J O ^b   Gerritsma, E ^b   Niermeyer, M F ^b   Hess, J ^b  

^a SOPHIA CHILDREN S HOSPITAL   (Netherlands)

^b NONE

Author keywords

22q11 deletion; Conotruncal heart defects; Velocardiofacial syndrome; Velopharyngeal insufficiency

Indexed keywords

ADOLESCENT; AORTA ARCH; ARTERIAL TRUNK; CHILD; CHROMOSOME 22Q; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CONFERENCE PAPER; CONGENITAL HEART DISEASE; CONGENITAL HEART MALFORMATION; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC COUNSELING; GREAT VESSELS TRANSPOSITION; HEART RIGHT VENTRICLE DOUBLE OUTLET; HUMAN; HUMAN CELL; INFANT; LUNG ATRESIA; MAJOR CLINICAL STUDY; MALE; NEWBORN; PHENOTYPE; PRESCHOOL CHILD; SCHOOL CHILD; SUBCLAVIAN ARTERY; TERATOLOGY; VELOCARDIOFACIAL SYNDROME;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; MALE; PHENOTYPE; PROSPECTIVE STUDIES; RETROSPECTIVE STUDIES; TRANSPOSITION OF GREAT VESSELS; VELOPHARYNGEAL INSUFFICIENCY;

EID: 0345059228     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (27)

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