Literature DB >> 2095701

An expanded mouse-human hybrid cell panel for mapping human chromosome 16.

D F Callen1, E Baker, H J Eyre, S A Lane.   

Abstract

A mouse/human hybrid cell panel of human chromosome 16 has been extended to a total of 31 hybrids. These hybrids were derived from constitutional translocations and deletions ascertained during clinical cytogenetic studies. This panel of hybrids, together with four fragile sites, have the potential to divide chromosome 16 into 38 regions. Rapid detailed physical mapping of gene probes or anonymous DNA probes is possible using this hybrid panel. This hybrid cell panel also allows the physical mapping of other chromosomes with three breakpoints on chromosomes 1, 4, 11 and 13 and two on chromosomes 3, 10 and 18.

Entities:  

Mesh：

Year:  1990        PMID： 2095701

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  6 in total

1.  The gene for the human IgA Fc receptor maps to 19q13.4.

Authors:  E J Kremer; V Kalatzis; E Baker; D F Callen; G R Sutherland; C R Maliszewski
Journal:  Hum Genet       Date:  1992-04       Impact factor: 4.132

2.  Dinucleotide repeat polymorphism at the D16S288 locus.

Authors:  Y Shen; K Holman; A Thompson; H Kozman; D F Callen; G R Sutherland; R I Richards
Journal:  Nucleic Acids Res       Date:  1991-10-11       Impact factor: 16.971

3.  An STS at the D16S290 locus.

Authors:  L Z Chen; Y Shen; K Holman; A Thompson; S Lane; R I Richards; G R Sutherland; D F Callen
Journal:  Nucleic Acids Res       Date:  1991-10-25       Impact factor: 16.971

4.  Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24.

Authors:  M A Pritchard; E Baker; D F Callen; G R Sutherland; A F Wilks
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

5.  Rubinstein-Taybi syndrome caused by submicroscopic deletions within 16p13.3.

Authors:  M H Breuning; H G Dauwerse; G Fugazza; J J Saris; L Spruit; H Wijnen; N Tommerup; C B van der Hagen; K Imaizumi; Y Kuroki; M J van den Boogaard; J M de Pater; E C Mariman; B C Hamel; H Himmelbauer; A M Frischauf; R Stallings; G C Beverstock; G J van Ommen; R C Hennekam
Journal:  Am J Hum Genet       Date:  1993-02       Impact factor: 11.025

6.  Isolation of a human DNA sequence which spans the fragile X.

Authors:  E J Kremer; S Yu; M Pritchard; R Nagaraja; D Heitz; M Lynch; E Baker; V J Hyland; R D Little; M Wada
Journal:  Am J Hum Genet       Date:  1991-09       Impact factor: 11.025
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.