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Literature DB >> 3290488

Genetic markers on chromosome 7.

Abstract

Chromosome 7 is frequently associated with chromosome aberrations, rearrangements, and deletions. It also contains many important genes, gene families, and disease loci. This brief review attempts to summarise these and other interesting aspects of chromosome 7. With the rapid accumulation of cloned genes and polymorphic DNA fragments, this chromosome has become an excellent substrate for molecular genetic studies.

Mesh：

Substances：
Genetic Markers

Year: 1988 PMID： 3290488 PMCID： PMC1050454 DOI： 10.1136/jmg.25.5.294

Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318

243 in total

1. Partial trisomy of 7q resulting from a familial translocation.

Authors: E Grace; G R Sutherland; G D Stark; A D Bain
Journal: Ann Genet Date: 1973-03

2. Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

Authors: M S Newton; C Cunningham; P A Jacobs; W H Price; I A Fraser
Journal: Clin Genet Date: 1972 Impact factor: 4.438

3. [Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation].

Authors: S Carpentier; M O Rethoré; J Lejeune
Journal: Ann Genet Date: 1972-12

4. Partial trisomy of the long arm of chromosome No. 7.

Authors: O S Alfi; G N Donnell; S L Kramer
Journal: J Med Genet Date: 1973-06 Impact factor: 6.318

5. [Structural and numerical chromosome abnormalities in human malignant melanoma cell lines (author's transl)].

Authors: S Bertrand; E Lefthériotis; J F Doré
Journal: C R Seances Acad Sci III Date: 1982-03-15

6. Ring chromosome 7 with variable phenotypic expression.

Authors: E H Zackai; W R Breg
Journal: Cytogenet Cell Genet Date: 1973

7. Chromosome 7 in ataxia-telangiectasia.

Authors: J M Scheres; T W Hustinx; C M Weemaes
Journal: J Pediatr Date: 1980-09 Impact factor: 4.406

8. Genetics of cell surface receptors for bioactive polypeptides: binding of epidermal growth factor is associated with the presence of human chromosome 7 in human-mouse cell hybrids.

Authors: N Shimizu; M A Behzadian; Y Shimizu
Journal: Proc Natl Acad Sci U S A Date: 1980-06 Impact factor: 11.205

Genetic markers on chromosome 7.

1. Partial trisomy of 7q resulting from a familial translocation.

2. Chromosome survey of a hospital for the mentally subnormal. 2. Autosome abnormalities.

3. [Partial 7q trisomy due to t(7;12) (q22;q24) familial translocation].

4. Partial trisomy of the long arm of chromosome No. 7.

5. [Structural and numerical chromosome abnormalities in human malignant melanoma cell lines (author's transl)].

6. Ring chromosome 7 with variable phenotypic expression.

7. Chromosome 7 in ataxia-telangiectasia.

8. Genetics of cell surface receptors for bioactive polypeptides: binding of epidermal growth factor is associated with the presence of human chromosome 7 in human-mouse cell hybrids.

9. A case of a paracentric inversion inv(7)(q11q22). Prenatal detection and counselling.

10. Evidence for a structural mutation of procollagen type I in a patient with the Ehlers-Danlos syndrome type VII.

1. Mortality from leukaemia among relatives of patients with cystic fibrosis.

2. In situ mapping of the muscle-specific form of phosphoglycerate mutase gene to human chromosome 7p12-7p13.

3. Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10.