Literature DB >> 6595199

Localisation of genetic markers and orientation of the linkage group on chromosome 19.

J D Brook, D J Shaw, L Meredith, G A Bruns, P S Harper.   

Abstract

A panel of human-rodent somatic cell hybrids containing translocation derivatives of human chromosome 19 has been used to assign the markers peptidase D, complement component 3, lysosomal mannosidase, lysosomal DNAase, chorionic gonadotropin beta-subunit, and a new polymorphic DNA sequence, to specific regions of chromosome 19. This has allowed the relative orientations of the genetic and physical maps to be established, and provides the framework for a search for the genes responsible for inherited disorders on chromosome 19, such as myotonic dystrophy and neurofibromatosis.

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Year:  1984        PMID: 6595199     DOI: 10.1007/bf00292584

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


  16 in total

1.  Confirmation of linkage of the loci for myotonic dystrophy and ABH secretion.

Authors:  J H Renwick; S E Bundey; M A Ferguson-Smith; M M Izatt
Journal:  J Med Genet       Date:  1971-12       Impact factor: 6.318

2.  Linkage between familial hypercholesterolemia with xanthomatosis and the C3 polymorphism confirmed.

Authors:  K Berg; A Heiberg
Journal:  Cytogenet Cell Genet       Date:  1978

Review 3.  Report of the Committee on the Genetic Constitution of Chromosomes 18, 19, 20, 21, and 22.

Authors:  A Westerveld; S Naylor
Journal:  Cytogenet Cell Genet       Date:  1984

4.  Assignment of the structural gene for the third component of human complement to chromosome 19.

Authors:  A S Whitehead; E Solomon; S Chambers; W F Bodmer; S Povey; G Fey
Journal:  Proc Natl Acad Sci U S A       Date:  1982-08       Impact factor: 11.205

5.  Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.

Authors:  K E Davies; J Jackson; R Williamson; P S Harper; S Ball; M Sarfarazi; L Meredith; G Fey
Journal:  J Med Genet       Date:  1983-08       Impact factor: 6.318

6.  Chromosome assignments in man of the genes for two hexosephosphate isomerases.

Authors:  F A McMorris; T R Chen; F Ricciuti; J Tischfield; R Creagan; F Ruddle
Journal:  Science       Date:  1973-03-16       Impact factor: 47.728

7.  Genetic evidence that a Y-linked gene in man is homologous to a gene on the X chromosome.

Authors:  P Goodfellow; G Banting; D Sheer; H H Ropers; A Caine; M A Ferguson-Smith; S Povey; R Voss
Journal:  Nature       Date:  1983 Mar 24-30       Impact factor: 49.962

8.  Coincidence of neurofibromatosis and myotonic dystrophy in a kindred.

Authors:  K Ichikawa; C J Crosley; A Culebras; L Weitkamp
Journal:  J Med Genet       Date:  1981-04       Impact factor: 6.318

9.  Expression of an X-linked gene from an inactive human X chromosome in mouse-human hybrid cells: further evidence for the noninactivation of the steroid sulfatase locus in man.

Authors:  T Mohandas; R S Sparkes; B Hellkuhl; K H Grzeschik; L J Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1980-11       Impact factor: 11.205

10.  The cDNA for the beta-subunit of human chorionic gonadotropin suggests evolution of a gene by readthrough into the 3'-untranslated region.

Authors:  J C Fiddes; H M Goodman
Journal:  Nature       Date:  1980-08-14       Impact factor: 49.962

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  27 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

2.  The physical map of chromosome arm 19q: some new assignments, confirmations and re-assessments.

Authors:  J D Brook; S J Knight; S H Roberts; H G Harley; K V Walsh; S A Rundle; K Freyne; M C Koch; N D Epstein; B Wieringa
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

3.  Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q.

Authors:  H G Harley; K V Walsh; S Rundle; J D Brook; M Sarfarazi; M C Koch; J L Floyd; P S Harper; D J Shaw
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

4.  Diagnosis of susceptibility to malignant hyperthermia with flanking DNA markers.

Authors:  S J Healy; J J Heffron; M Lehane; D G Bradley; K Johnson; T V McCarthy
Journal:  BMJ       Date:  1991-11-16

Review 5.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

6.  Absence of a single repeat from the coding region of the human involucrin gene leading to RFLP.

Authors:  M Simon; M Phillips; H Green; H Stroh; K Glatt; G Burns; S A Latt
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

7.  The 35 kd pulmonary surfactant-associated protein is encoded on chromosome 10.

Authors:  G Bruns; H Stroh; G M Veldman; S A Latt; J Floros
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

8.  A highly polymorphic locus in human DNA revealed by probes from cosmid 1-5 maps to chromosome 2q35----37.

Authors:  M Litt; G A Bruns; R Sheehy; R E Magenis
Journal:  Am J Hum Genet       Date:  1986-03       Impact factor: 11.025

9.  Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.

Authors:  L Bufton; G A Bruns; R E Magenis; D Tomar; D Shaw; D Brook; M Litt
Journal:  Am J Hum Genet       Date:  1986-04       Impact factor: 11.025

10.  Exclusion of the Friedreich ataxia gene from chromosome 19.

Authors:  S Chamberlain; C S Worrall; S South; J Shaw; M Farrall; R Williamson
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

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