Case Reports
[Del(1)(q22-q25) syndrome. Cytogenetics and phenotype]
[Article in
Russian]
- PMID: 3617217
Item in Clipboard
Case Reports
[Del(1)(q22-q25) syndrome. Cytogenetics and phenotype]
[Article in
Russian]
Tsitol Genet.
1987 May-Jun.
Abstract
A male infant is described with dysmorphology of the head and face, neck, extremities and genitalia, as well as growth and mental retardation and with the de novo interstitial deletion of the proximal segment of the long arm of chromosome 1-del (1) (q22-q25). Comparison of the phenotypic characteristics of this patient with those of previously described patients with similar deletion confirms the existence of the proximal 1q deletion syndrome.
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