Literature DB >> 7774955

The CEPH consortium linkage map of human chromosome 16.

H M Kozman1, T P Keith, H Donis-Keller, R L White, J Weissenbach, M Dean, G Vergnaud, K Kidd, J Gusella, N J Royle.   

Abstract

A Centre d'Etude du Polymorphisme Humain (CEPH) consortium map of human chromosome 16 has been constructed. The map contains 158 loci defined by 191 different probe/restriction enzyme combinations or primer pairs. The marker genotypes, contributed by 9 collaborating laboratories, originated from the CEPH families DNA. A total of 60 loci, with an average heterozygosity of 68%, have been placed on the framework genetic map. The genetic map contains 7 genes. The length of the sex-averaged map is 165 cM, with a mean genetic distance between loci of 2.8 cM; the median distance between markers is 2.0 cM. The male map length is 136 cM, and the female map length is 197 cM. The map covers virtually the entire chromosome, from D16S85, within 170 to 430 kb of the 16p telomere, to D16S303 at 16qter. The markers included in the linkage map have been physically mapped on a partial human chromosome 16 somatic cell hybrid panel, thus anchoring the genetic map to the cytogenetic-based physical map.

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Year:  1995        PMID: 7774955     DOI: 10.1016/0888-7543(95)80108-x

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  8 in total

1.  Linkage disequilibrium mapping places the gene causing familial Mediterranean fever close to D16S246.

Authors:  E N Levy; Y Shen; A Kupelian; L Kruglyak; I Aksentijevich; E Pras; J E Balow; B Linzer; X Chen; D A Shelton; D Gumucio; M Pras; M Shohat; J I Rotter; N Fischel-Ghodsian; R I Richards; D L Kastner
Journal:  Am J Hum Genet       Date:  1996-03       Impact factor: 11.025

2.  Report of a critical recombination further narrowing the TSC1 region.

Authors:  K S Au; J Murrell; A Buckler; S H Blanton; H Northrup
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

3.  Genetic heterogeneity in familial acute myelogenous leukemia: evidence for a second locus at chromosome 16q21-23.2.

Authors:  M Horwitz; K F Benson; F Q Li; J Wolff; M F Leppert; L Hobson; M Mangelsdorf; S Yu; D Hewett; R I Richards; W H Raskind
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

4.  Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16.

Authors:  P Szepetowski; J Rochette; P Berquin; C Piussan; G M Lathrop; A P Monaco
Journal:  Am J Hum Genet       Date:  1997-10       Impact factor: 11.025

5.  Localization of a breast cancer tumour-suppressor gene to a 3-cM interval within chromosomal region 16q22.

Authors:  A Iida; R Isobe; M Yoshimoto; F Kasumi; Y Nakamura; M Emi
Journal:  Br J Cancer       Date:  1997       Impact factor: 7.640

6.  Allelic loss of chromosome 16q in endometrial cancer: correlation with poor prognosis of patients and less differentiated histology.

Authors:  T Kihana; N Yano; S Murao; H Iketani; K Hamada; J Yano; S Murao; H Iketani; K Hamada; J Yano; S Matsuura
Journal:  Jpn J Cancer Res       Date:  1996-11

7.  Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour.

Authors:  R G Grundy; J Pritchard; P Scambler; J K Cowell
Journal:  Br J Cancer       Date:  1998-11       Impact factor: 7.640

8.  Association of replication error positive phenotype with lymphocyte infiltration in endometrial cancers.

Authors:  T Kihana; T Fujioka; K Hamada; K Kito; A Takahashi; C Tsukayama; M Ito
Journal:  Jpn J Cancer Res       Date:  1998-09
  8 in total

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