Cytogenetic and clinical findings in a patient with a deletion of 16q23.1: First report of bilateral cataracts and a 16q deletion

American Journal of Medical Genetics

Volumn 73, Issue 2, 1997, Pages 180-183

  Monaghan, Kristin G ^a   Van Dyke, Daniel L ^a   Wiktor, Anne ^a   Feldman, Gerald L ^a  

^a HENRY FORD HOSPITAL   (United States)

Author keywords

16q23.1; Cataracts; Deletion syndrome

Indexed keywords

ARTICLE; CASE REPORT; CATARACT; CHILD; CHROMOSOME 16Q; CRANIOFACIAL MALFORMATION; CYTOGENETICS; GENE DELETION; GENE ISOLATION; HUMAN; HYPERTELORISM; IRIS COLOBOMA; LOW SET EAR; MALE; MUSCLE HYPOTONIA; MUSCULOSKELETAL SYSTEM MALFORMATION; PALPEBRAL FISSURE ANOMALY; PES EQUINOVARUS; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; AUTISTIC DISORDER; CATARACT; CHILD, PRESCHOOL; CHROMOSOME ABERRATIONS; CHROMOSOME DELETION; CHROMOSOME DISORDERS; CHROMOSOMES, HUMAN, PAIR 16; COLOBOMA; CRANIOFACIAL ABNORMALITIES; GROWTH DISORDERS; HUMANS; IRIS; MALE; MUSCLE HYPOTONIA; PSYCHOMOTOR DISORDERS;

EID: 0030734494     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(1997)73:2<180::AID-AJMG13>3.0.CO;2-Q     Document Type: Article

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