Literature DB >> 422198

Translocation C:D involving chromosomes 11 and 14.

M H Callow, A R Boon, E V Davison.   

Abstract

A translocation of material from chromosome 11 to chromosome 14 was identified in a 7-month-old male with microcephaly and developmental delay. The break-points appear to be on the long arm of chromosome 11, close to the centromere, and on the short arm of the 14.

Entities:  

Mesh：

Year:  1979        PMID： 422198     DOI： 10.1007/bf00291915

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  7 in total

1.  Ring chromosome 13 syndrome.

Authors:  K Fried; M Rosenblatt; G Mundel; R Krikler
Journal:  Clin Genet       Date:  1975-03       Impact factor: 4.438

2.  Chromosome preparations of leukocytes cultured from human peripheral blood.

Authors:  P S MOORHEAD; P C NOWELL; W J MELLMAN; D M BATTIPS; D A HUNGERFORD
Journal:  Exp Cell Res       Date:  1960-09       Impact factor: 3.905

3.  Microcephaly, mental retardation and hypertelorism in chromosome deletion studies.

Authors:  J Q Miller
Journal:  Neurology       Date:  1973-11       Impact factor: 9.910

4.  Developmental abnormalities associated with a ring chromosome 6.

Authors:  C M Moore; R H Heller; G H Thomas
Journal:  J Med Genet       Date:  1973-09       Impact factor: 6.318

5.  A family with a chromosome 14 short arm deletion.

Authors:  J Nielsen; A B Hreidarsson; T Brynjolfsson; V Holm; A M Madsen; G B Petersen; L Lamm; P Saldańa-Garcia
Journal:  Hereditas       Date:  1978       Impact factor: 3.271

6.  A ring-20 chromosome.

Authors:  L Atkins; W L Miller; M Salam
Journal:  J Med Genet       Date:  1972-09       Impact factor: 6.318

Review 7.  Autosomal reciprocal translocations and 13/14 translocations: a population study.

Authors:  J Nielsen; K Rasmussen
Journal:  Clin Genet       Date:  1976-09       Impact factor: 4.438
  7 in total

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