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

Kozma, C; Chong, S S; Meck, J M

Kozma, C; Chong, S S; Meck, J M.

Affiliation

Kozma C; Child Development Center/Department of Pediatrics, Georgetown University Medical Center, Washington, DC 20007-3935, USA.

Am J Med Genet ; 86(4): 316-20, 1999 Oct 08.

Article in En | MEDLINE | ID: mdl-10494085

Subject(s)

Abnormalities, Multiple/genetics; Chromosome Deletion; Chromosomes, Human, Pair 4/genetics; Deafness/genetics; Tooth Abnormalities/genetics; Child; Humans; Intelligence; Male; Phenotype; Physical Chromosome Mapping; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Tooth Abnormalities / Abnormalities, Multiple / Chromosomes, Human, Pair 4 / Chromosome Deletion / Deafness Limits: Child / Humans / Male Language: En Journal: Am J Med Genet Year: 1999 Document type: Article

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