Literature DB >> 2037294

The CEPH consortium linkage map of human chromosome 1.

N C Dracopoli1, P O'Connell, T I Elsner, J M Lalouel, R L White, K H Buetow, D Y Nishimura, J C Murray, C Helms, S K Mishra.   

Abstract

This paper describes the Centre d'Etude du Polymorphisme Humain (CEPH) consortium linkage map of human chromosome 1. The map contains 101 loci defined by genotypes generated from CEPH family DNAs with 146 different contributions from 11 laboratories. A total of 58 loci are uniquely placed on the map with likelihood support of at least 1000:1. The map extends from loci in the terminal bands of both chromosome arms (locus D1Z2 in 1p36.3 and D1S68 in 1q44) and is anchored at the centromere by the D1Z5 alpha-satellite polymorphism. With the exception of a single locus, the remaining loci are arrayed on the fixed map in short intervals and their possible locations are indicated. Multipoint linkage analyses provided estimates that the male, female, and sex-averaged maps extend for 308, 478, and 390 cM, respectively. The sex-averaged map contains only four intervals greater than 15 cM, and the mean genetic distance between the 58 uniquely placed loci is 6.7 cM.

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Year:  1991        PMID: 2037294     DOI: 10.1016/0888-7543(91)90362-i

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


  24 in total

1.  A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.

Authors:  J A Douglas; M Boehnke; K Lange
Journal:  Am J Hum Genet       Date:  2000-03-28       Impact factor: 11.025

2.  Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I.

Authors:  N G Laing; B T Majda; P A Akkari; M G Layton; J C Mulley; H Phillips; E A Haan; S J White; A H Beggs; L M Kunkel
Journal:  Am J Hum Genet       Date:  1992-03       Impact factor: 11.025

3.  Integration of gene maps: chromosome 1.

Authors:  A Collins; B J Keats; N Dracopoli; D C Shields; N E Morton
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205

4.  Influence of aberrant observations on high-resolution linkage analysis outcomes.

Authors:  K H Buetow
Journal:  Am J Hum Genet       Date:  1991-11       Impact factor: 11.025

5.  Error filtration, interference, and the human linkage map.

Authors:  D C Shields; A Collins; K H Buetow; N E Morton
Journal:  Proc Natl Acad Sci U S A       Date:  1991-08-01       Impact factor: 11.205

6.  Radiation hybrid mapping.

Authors:  S Lawrence; N E Morton; D R Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1991-09-01       Impact factor: 11.205

7.  Fragile-X syndrome: unique genetics of the heritable unstable element.

Authors:  S Yu; J Mulley; D Loesch; G Turner; A Donnelly; A Gedeon; D Hillen; E Kremer; M Lynch; M Pritchard
Journal:  Am J Hum Genet       Date:  1992-05       Impact factor: 11.025

Review 8.  Tear lipocalin and the eye's front line of defence.

Authors:  A M Gachon; E Lacazette
Journal:  Br J Ophthalmol       Date:  1998-04       Impact factor: 4.638

Review 9.  Red blood cell polymorphism and susceptibility to Plasmodium vivax.

Authors:  Peter A Zimmerman; Marcelo U Ferreira; Rosalind E Howes; Odile Mercereau-Puijalon
Journal:  Adv Parasitol       Date:  2013       Impact factor: 3.870

10.  Recurrent 1;17 translocations in human neuroblastoma reveal nonhomologous mitotic recombination during the S/G2 phase as a novel mechanism for loss of heterozygosity.

Authors:  H Caron; P van Sluis; N van Roy; J de Kraker; F Speleman; P A Voûte; A Westerveld; R Slater; R Versteeg
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

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