Velo-cardio-facial and partial DiGeorge phenotype in a child with interstitial deletion at 10p13-implications for cytogenetics and molecular biology

American Journal of Medical Genetics

Volumn 65, Issue 4, 1996, Pages 304-308

  Lipson, Anthony ^a   Fagan, Kerry ^b   Colley, Alison ^c,d   Colley, Peter ^b   Sholler, Gary ^a   Issacs, David ^a   Oates, R Kim ^a  

^a CHILDREN S HOSPITAL AT WESTMEAD   (Australia)

^b JOHN HUNTER HOSPITAL   (Australia)

^c Hunter Genetics   (Australia)

^d LIVERPOOL HOSPITAL   (Australia)

Author keywords

chromosome 10; chromosome 22; DiGeorge; interstitial deletion; velo cardio facial

Indexed keywords

ARTICLE; CASE REPORT; CHROMOSOME 10P; CHROMOSOME 22; CHROMOSOME ANALYSIS; CLEFT PALATE; DEVELOPMENTAL DISORDER; DIGEORGE SYNDROME; FEMALE; HEART VENTRICLE SEPTUM DEFECT; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; INTERSTITIAL CHROMOSOME DELETION; JOINT CONTRACTURE; MANDIBLE HYPOPLASIA; MAXILLA HYPOPLASIA; MICROTIA; NOSE MALFORMATION; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; SWALLOWING; T LYMPHOCYTE SUBPOPULATION;

ABNORMALITIES, MULTIPLE; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 10; DIGEORGE SYNDROME; EAR; FACE; FEMALE; GENE DELETION; HUMANS; INFANT; PHENOTYPE;

MICROTIA;

EID: 0029835883     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961111)65:4<304::AID-AJMG11>3.0.CO;2-Y     Document Type: Article

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