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Literature DB >> 4134839

An analysis of the break points of structural rearrangements in man.

P A Jacobs, K E Buckton, C Cunningham, M Newton.

Abstract

Entities: Species

Mesh：

Year: 1974 PMID： 4134839 PMCID： PMC1013088 DOI： 10.1136/jmg.11.1.50

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

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12 in total

1. New technique for distinguishing between human chromosomes.

Authors: A T Sumner; H J Evans; R A Buckland
Journal: Nat New Biol Date: 1971-07-07

2. Distinguishing between the chromosomes involved in Down's syndrome (trisomy 21) and cronic myeloid leukaemia (Ph1) by fluorescence.

Authors: M L O'Riordan; J A Robinson; K E Buckton; H J Evans
Journal: Nature Date: 1971-03-19 Impact factor: 49.962

3. Incidence and mutation rates of structural rearrangements of the autosomes in man.

Authors: P A Jacobs; A Frackiewicz; P Law
Journal: Ann Hum Genet Date: 1972-03 Impact factor: 1.670

4. The chromosomal constitution of 165 human translocations involving D group chromosomes identified by autoradiography.

Authors: M M Cohen
Journal: Ann Genet Date: 1971-06

5. Radiation-induced non-random chromosome breakage.

Authors: T Caspersson; U Haglund; B Lindell; L Zech
Journal: Exp Cell Res Date: 1972-12 Impact factor: 3.905

6. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.

Authors: U Francke
Journal: Am J Hum Genet Date: 1972-03 Impact factor: 11.025

7. Patterns of D chromosome involvement in human (DqDq) and (DqGq) Robertsonian rearrangements.

Authors: F Hecht; W J Kimberling
Journal: Am J Hum Genet Date: 1971-07 Impact factor: 11.025

8. [Autoradiographic studies of human chromosomes. VII. 5 cases of familial t(DqDq)].

Authors: J de Grouchy; L Crippa; J German
Journal: Ann Genet Date: 1970-03

9. Possible non random selection of D group chromosomes involved in centric-fusion translocations.

Authors: J D Rowley; E Pergament
Journal: Ann Genet Date: 1969-09

10. Pericentric inversion of a group C autosome: a study of three families.

Authors: P A Jacobs; G Cruickshank; M J Faed; A Frackiewicz; E B Robson; H Harris; I Sutherland
Journal: Ann Hum Genet Date: 1968-01 Impact factor: 1.670

62 in total

1. Translocation (13q21q). Four generation family study with analysis of satellite associations, fluorescent markers, and prenatal diagnosis.

Authors: M Mikkelsen; A Hansson; P Jacobsen; N Hobolth
Journal: Humangenetik Date: 1975

2. Specific chromosome aberrations in ataxia telangiectasia.

Authors: J M Oxford; D G Harnden; J M Parrington; J D Delhanty
Journal: J Med Genet Date: 1975-09 Impact factor: 6.318

3. Association of pericentric inversion of chromosome 9 and reproductive failure in ten unrelated families.

Authors: J Boué; J L Taillemite; P Hazael-Massieux; C Léonard; A Boué
Journal: Humangenetik Date: 1975-09-20

4. Report of large kinship with familial translocation between chromosomes 21 and 22.

Authors: J E Brissenden; M T Costa; M H Roberts
Journal: Can Med Assoc J Date: 1977-12-17 Impact factor: 8.262

Review 5. The critical region on the human Xq.

Authors: E Therman; R Laxova; B Susman
Journal: Hum Genet Date: 1990-10 Impact factor: 4.132