Literature DB >> 6336311

Genetic mapping: X chromosome.

B Keats.   

Abstract

Starting with the male chiasma distribution for chromosome 2, a significantly better fit is obtained to lod scores for the X chromosome if terminalization of distal chiasmata is assumed. The linkage data are not consistent with a uniform distribution of chiasmata, absence of terminalization, or restriction of terminalization to the distal band. As information about the genetic map of the X chromosome increases, the map will be freed from assumptions about chiasma distribution. At present, however, even fragmentary data on the male are useful to construct a genetic map that, by converting physical assignments to equivalent genetic recombinations, has no inconsistencies between genetic and physical map orders.

Mesh:

Substances:

Year:  1983        PMID: 6336311     DOI: 10.1007/bf00289474

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  22 in total

1.  A new estimate of the linkage between the genes for colourblindness and haemophilia in man.

Authors:  J B S HALDANE; C A B SMITH
Journal:  Ann Eugen       Date:  1947-10

2.  Linkage relations of X-borne ichthyosis to the Xg blood groups and to other markers of the X in Israelis.

Authors:  A Adam; L Ziprkowski; A Feinstein; R Sanger; P Tippett; J Gavin; R R Race
Journal:  Ann Hum Genet       Date:  1969-05       Impact factor: 1.670

3.  A chiasma map of man.

Authors:  N E Morton; D C Rao; J Lindsten; M Hultén; S Yee
Journal:  Hum Hered       Date:  1977       Impact factor: 0.444

4.  Chiasma frequency and distribution in a sample of human males: chromosomes 1, 2, and 9.

Authors:  D A Laurie; M Hultén; G H Jones
Journal:  Cytogenet Cell Genet       Date:  1981

5.  X-linkage and genetic heterogeneity in bipolar-related major affective illness: reanalysis of linkage data.

Authors:  N Risch; M Baron
Journal:  Ann Hum Genet       Date:  1982-05       Impact factor: 1.670

6.  Genetic mapping: chromosomes 2-5.

Authors:  B Keats
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

7.  Familial X-linked mental retardation with an X chromosome abnormality.

Authors:  J Harvey; C Judge; S Wiener
Journal:  J Med Genet       Date:  1977-02       Impact factor: 6.318

8.  Adrenoleukodystrophy: evidence for X linkage, inactivation, and selection favoring the mutant allele in heterozygous cells.

Authors:  B R Migeon; H W Moser; A B Moser; J Axelman; D Sillence; R A Norum
Journal:  Proc Natl Acad Sci U S A       Date:  1981-08       Impact factor: 11.205

9.  An international system for human cytogenetic nomenclature--high-resolution banding (1981). ISCN (1981). Report of the Standing Committee on Human Cytogenetic Nomenclature.

Authors: 
Journal:  Cytogenet Cell Genet       Date:  1981

10.  Localization of loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase and biochemical evidence of nonrandom X chromosome expression from studies of a human X-autosome translocation.

Authors:  G S Pai; J A Sprenkle; T T Do; C E Mareni; B R Migeon
Journal:  Proc Natl Acad Sci U S A       Date:  1980-05       Impact factor: 11.205

View more
  9 in total

1.  The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Authors:  I Oberlé; D Drayna; G Camerino; R White; J L Mandel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

2.  X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Authors:  U Friedrich; M Warburg; P Wieacker; T F Wienker; A Gal; H H Ropers
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

3.  Emery-Dreifuss muscular dystrophy: localisation to Xq27.3----qter confirmed by linkage to the factor VIII gene.

Authors:  J R Yates; N A Affara; D M Jamieson; M A Ferguson-Smith; I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; A W Johnston; K Kelly
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

4.  Linkage analysis using multiple Xq DNA polymorphisms in normal families, families with the fragile X syndrome, and other families with X linked conditions.

Authors:  J M Connor; L A Pirrit; J R Yates; J A Crossley; S J Imrie; J M Colgan
Journal:  J Med Genet       Date:  1987-01       Impact factor: 6.318

Review 5.  On the genetic length of the short arm of the human X chromosome.

Authors:  H H Ropers; P Wieacker; T F Wienker; K Davies; R Williamson
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Genetic mapping of DNA segments relative to the locus for the fragile-X syndrome at Xq27.3.

Authors:  L M Mulligan; M A Phillips; C J Forster-Gibson; J Beckett; M W Partington; N E Simpson; J J Holden; B N White
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

7.  Assignment of the gene for dyskeratosis congenita to Xq28.

Authors:  J M Connor; D Gatherer; F C Gray; L A Pirrit; N A Affara
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

8.  Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm.

Authors:  M Purrello; R Nussbaum; A Rinaldi; G Filippi; S Traccis; B Latte; M Siniscalco
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

9.  Incontinentia pigmenti and X-autosome translocations. Non-isotopic in situ hybridization with an X-centromere-specific probe (pSV2X5) reveals a possible X-centromeric breakpoint in one of five published cases.

Authors:  J A Crolla; S Gilgenkrantz; J de Grouchy; T Kajii; M Bobrow
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.