Literature DB >> 1427835

Genetic and physical maps of human chromosome 4 based on dinucleotide repeats.

K A Mills1, K H Buetow, Y Xu, J L Weber, M R Altherr, J J Wasmuth, J C Murray.   

Abstract

Characterization of inherited variations within tandem arrays of dinucleotide repeats has substantially advanced the construction of genetic maps using linkage approaches over the last several years. Using a backbone of 10 newly identified microsatellite repeats on human chromosome 4 and 6 previously identified short tandem repeat element polymorphisms, we have constructed several genetic maps and a physical map of human chromosome 4. The genetic and physical maps are in complete concordance with each other. The genetic maps include a 15-locus microsatellite-based linkage map, a framework map of high support incorporating a total of 39 independent loci, a 25-locus high-heterozygosity, easily used index map, and a gene-based comprehensive map that provides the best genetic location for 35 genes mapped to chromosome 4. The 16 microsatellite markers are each localized to one of nine regions of chromosome 4, delineated by a panel of somatic cell hybrids. These results demonstrate the utility of PCR-based repeat elements for the construction of genetic maps and provide a valuable resource for continued high-resolution mapping of chromosome 4 and of genetic disorders to this chromosome.

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Year:  1992        PMID: 1427835     DOI: 10.1016/s0888-7543(05)80208-3

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


  19 in total

1.  Identification and genetic mapping of a homeobox gene to the 4p16.1 region of human chromosome 4.

Authors:  H S Stadler; B J Padanilam; K Buetow; J C Murray; M Solursh
Journal:  Proc Natl Acad Sci U S A       Date:  1992-12-01       Impact factor: 11.205

2.  The Ant1 gene maps near Klk3 on proximal mouse chromosome 8.

Authors:  K A Mills; J W Ellison; K D Mathews
Journal:  Mamm Genome       Date:  1996-09       Impact factor: 2.957

3.  Autosomal dominant polycystic kidney disease: evidence for the existence of a third locus in a Portuguese family.

Authors:  S de Almeida; E de Almeida; D Peters; J R Pinto; I Távora; J Lavinha; M Breuning; M M Prata
Journal:  Hum Genet       Date:  1995-07       Impact factor: 4.132

4.  Genetic heterogeneity of polycystic kidney disease in Bulgaria.

Authors:  N Bogdanova; B Dworniczak; D Dragova; V Todorov; D Dimitrakov; K Kalinov; J Hallmayer; J Horst; L Kalaydjieva
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

5.  A syntrophin gene maps to mouse chromosome 8 and is not the myodystrophy gene.

Authors:  K A Mills; Y Sunada; K P Campbell; K D Mathews
Journal:  Mamm Genome       Date:  1995-09       Impact factor: 2.957

6.  Polymorphism and phylogeny of dinucleotide repeats in human T-cell receptor Vb6 genes.

Authors:  P Charmley; P Concannon
Journal:  Immunogenetics       Date:  1993       Impact factor: 2.846

Review 7.  Toward the complete genomic map and molecular pathology of human chromosome 4.

Authors:  O Riess; B Winkelmann; J T Epplen
Journal:  Hum Genet       Date:  1994-07       Impact factor: 4.132

8.  Genetic heterogeneity in adult dominant polycystic kidney disease in Cypriot families.

Authors:  C D Constantinou-Deltas; E Papageorgiou; K Boteva; K Christodoulou; M H Breuning; D J Peter; A Pierides
Journal:  Hum Genet       Date:  1995-04       Impact factor: 4.132

9.  Genetic mapping near the myd locus on mouse chromosome 8.

Authors:  K A Mills; K D Mathews; T Scherpbier-Heddema; R L Schelper; R Schmalzel; H L Bailey; J H Nadeau; K H Buetow; J C Murray
Journal:  Mamm Genome       Date:  1995-04       Impact factor: 2.957

10.  Detection of maternal cell contamination in amniotic fluid cell cultures using fluorescent labelled microsatellites.

Authors:  G W Smith; C A Graham; J Nevin; N C Nevin
Journal:  J Med Genet       Date:  1995-01       Impact factor: 6.318

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