Literature DB >> 2127363

Chiasma-based genetic maps of chromosome 21.

M Hultén1, N M Lawrie, D A Laurie.   

Abstract

The available cytogenetic data on meiotic chiasmata have been used to construct sex-specific genetic maps, showing the genetic distances and recombination fractions along the length of 21q. The male maps are based on direct observations of spermatocytes, while the female maps are derivations related to the increased chromosome length in oocytes. The male chiasma data have also been used as a frame of reference for ordering and positioning loci on the physical map with D21S110 as a fixed point.

Mesh:

Year:  1990        PMID: 2127363     DOI: 10.1002/ajmg.1320370730

Source DB:  PubMed          Journal:  Am J Med Genet Suppl        ISSN: 1040-3787


  7 in total

1.  Characterization of human crossover interference.

Authors:  K W Broman; J L Weber
Journal:  Am J Hum Genet       Date:  2000-05-08       Impact factor: 11.025

2.  Crossover distribution in barley analysed through RFLP linkage data.

Authors:  T Säll; N O Nilsson
Journal:  Theor Appl Genet       Date:  1994-10       Impact factor: 5.699

3.  Estimating meiotic exchange patterns from recombination data: an application to humans.

Authors:  N E Lamb; E Feingold; S L Sherman
Journal:  Genetics       Date:  1997-07       Impact factor: 4.562

4.  Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat-polymorphism linkage map of chromosome 19.

Authors:  J L Weber; Z Wang; K Hansen; M Stephenson; C Kappel; S Salzman; P J Wilkie; B Keats; N C Dracopoli; B F Brandriff
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

5.  Chiasma-based genetic map of the mouse X chromosome.

Authors:  M A Hultén; C Tease; N M Lawrie
Journal:  Chromosoma       Date:  1995-11       Impact factor: 4.316

6.  On the origin of crossover interference: A chromosome oscillatory movement (COM) model.

Authors:  Maj A Hultén
Journal:  Mol Cytogenet       Date:  2011-04-08       Impact factor: 2.009

7.  Meiotic crossing-over in nondisjoined chromosomes of children with trisomy 21 and a congenital heart defect.

Authors:  C M Howard; G E Davies; M J Farrer; L M Cullen; M M Coleman; R Williamson; R K Wyse; R Palmer; A M Kessling
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025

  7 in total

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