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Interstitial deletion 11q. Case report and review of the literature.
De Pater, J M; Ippel, P F; Bijlsma, J B; Van Nieuwenhuizen, O.
Affiliation
  • De Pater JM; Clinical Genetics Centre, Wilhelmina Children's Hospital, Utrecht.
Genet Couns ; 8(4): 335-9, 1997.
Article in En | MEDLINE | ID: mdl-9457504
ABSTRACT
A mildly retarded male with a unique interstitial deletion 11 (pter-->q22.3q23.2-->qter) is described. To the best of our knowledge this patient is the first case with this specific type of deletion. The clinical features and cytogenetic findings of this patient are compared with those of previously reported cases with interstitial deletions 11q and patients with terminal deletions involving band 11q24.1 (leading to the so-called Jacobsen syndrome).
Subject(s)
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Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 11 / Chromosome Deletion / Intellectual Disability / Monosomy Limits: Humans / Male Language: En Year: 1997 Type: Article
Search on Google
Database: MEDLINE Main subject: Abnormalities, Multiple / Chromosomes, Human, Pair 11 / Chromosome Deletion / Intellectual Disability / Monosomy Limits: Humans / Male Language: En Year: 1997 Type: Article