Interstitial deletion of 4p15.32p16.3 in a boy with minor anomalies, hearing loss, borderline intelligence, and oligodontia

American Journal of Medical Genetics

Volumn 86, Issue 4, 1999, Pages 316-320

  Kozma, Chahira ^a   Chong, Samuel S ^a   Meek, Jeanne M ^a  

^a GEORGETOWN UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

Chromosome 4; Hearing loss; Interstitial deletion; Oligodontia; Wolf Hirschhorn syndrome

Indexed keywords

AMBLYOPIA; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 4P; CHROMOSOME DELETION 4; HEARING LOSS; HUMAN; MALE; MENTAL DEFICIENCY; OLIGODONTIA; PRIORITY JOURNAL; SHORT STATURE; WOLF HIRSCHHORN SYNDROME;

ABNORMALITIES, MULTIPLE; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 4; DEAFNESS; HUMANS; INTELLIGENCE; MALE; PHENOTYPE; PHYSICAL CHROMOSOME MAPPING; SYNDROME; TOOTH ABNORMALITIES;

CANIS;

EID: 0032848996     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19991008)86:4<316::AID-AJMG3>3.0.CO;2-1     Document Type: Article

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