Literature DB >> 8325627

A linkage map of human chromosome 21:43 PCR markers at average intervals of 2.5 cM.

M G McInnis1, A Chakravarti, J Blaschak, M B Petersen, V Sharma, D Avramopoulos, J L Blouin, U König, C Brahe, T C Matise.   

Abstract

A genetic linkage map of human chromosome 21q (HC21q) containing 43 markers genotyped by the polymerase chain reaction in the CEPH pedigrees is presented. The markers placed on this map are highly polymorphic with an average heterozygosity of 61%. The average interval size of the markers localized at 1000:1 odds is 2.5 cM. The map has a total length of 65.5 cM, with male and female lengths of 47.7 and 83.3 cM, respectively. The genotypes used in the construction of this map were subjected to rigorous error checking, which is reflected in the shorter map length compared to previous maps; the estimated error rate in genotyping is less than 0.04%. As noted in previous linkage maps there is increased recombination in females on proximal HC 21q and in the male in a region near the telomere. This map of HC 21 represents a highly informative and dense meiotic linkage map and will be useful in linking disease phenotypes to loci on this chromosome.

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Year:  1993        PMID: 8325627     DOI: 10.1006/geno.1993.1231

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


  20 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.  Cloning of the cDNA for a human homologue of the Drosophila white gene and mapping to chromosome 21q22.3.

Authors:  H Chen; C Rossier; M D Lalioti; A Lynn; A Chakravarti; G Perrin; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

3.  The human lanosterol synthase gene maps to chromosome 21q22.3.

Authors:  M Young; H Chen; M D Lalioti; S E Antonarakis
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

4.  Down syndrome: characterisation of a case with partial trisomy of chromosome 21 owing to a paternal balanced translocation (15;21) (q26;q22.1) by FISH.

Authors:  M Nadal; S Moreno; M Pritchard; M A Preciado; X Estivill; M A Ramos-Arroyo
Journal:  J Med Genet       Date:  1997-01       Impact factor: 6.318

5.  Molecular mapping of 21 features associated with partial monosomy 21: involvement of the APP-SOD1 region.

Authors:  Z Chettouh; M F Croquette; B Delobel; S Gilgenkrants; C Leonard; C Maunoury; M Prieur; M O Rethoré; P M Sinet; M Chery
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

6.  Double non-disjunction in maternal meiosis II giving rise to a fetus with 48,XXX,+21.

Authors:  V M Park; R R Bravo; L P Shulman
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

7.  Characterisation of three microsatellite polymorphisms (D21S1262, D21S1419 and D21S1421) from band 21q22.1.

Authors:  A Bosch; J Guimerà; D Patterson; X Estivill
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

8.  Physical structure of human chromosome 21: an analysis of YACs spanning 21q.

Authors:  H Ochman; L A Buckholtz
Journal:  Mamm Genome       Date:  1995-02       Impact factor: 2.957

9.  Statistical analysis of crossover interference using the chi-square model.

Authors:  H Zhao; T P Speed; M S McPeek
Journal:  Genetics       Date:  1995-02       Impact factor: 4.562

10.  Normal phenotype with paternal uniparental isodisomy for chromosome 21.

Authors:  J L Blouin; D Avramopoulos; C Pangalos; S E Antonarakis
Journal:  Am J Hum Genet       Date:  1993-11       Impact factor: 11.025

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