Contiguous gene syndromes: A component of recognizable syndromes

The Journal of Pediatrics

Volumn 109, Issue 2, 1986, Pages 231-241

  Schmickel, Roy D ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AASE SYNDROME; ANIRIDIA; BECKWITH WIEDEMANN SYNDROME; CHILD; CHONDRODYSPLASIA; CHROMOSOME DELETION; CHROMOSOME DUPLICATION; CHROMOSOME TRANSLOCATION; CLASSIFICATION; CONGENITAL DISORDER; DIAGNOSIS; DIGEORGE SYNDROME; ETIOLOGY; GENE DELETION; GONADOBLASTOMA; HEREDITY; HISTOLOGY; HUMAN; KIDNEY; MALFORMATION SYNDROME; MENTAL DEFICIENCY; MENTAL RETARDATION MALFORMATION SYNDROME; MILLER DIEKER SYNDROME; NEPHROBLASTOMA; PARTIAL MONOSOMY; PRADER WILLI SYNDROME; PRIORITY JOURNAL; RETINOBLASTOMA; REVIEW; RUBINSTEIN SYNDROME; URINARY TRACT; UROGENITAL TRACT MALFORMATION; VISUAL SYSTEM;

ABNORMALITIES; BECKWITH-WIEDEMANN SYNDROME; CHILD; CHROMOSOME ABERRATIONS; CHROMOSOME DISORDERS; CHROMOSOME MAPPING; DIGEORGE SYNDROME; GENETIC DISEASES, INBORN; HUMAN; IRIS; KIDNEY NEOPLASMS; NEPHROBLASTOMA; PRADER-WILLI SYNDROME; RETINOBLASTOMA; SYNDROME; VARIATION (GENETICS);

EID: 0022916035     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(86)80377-8     Document Type: Article

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