Literature DB >> 2877935

Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus.

M H Hofker, G J van Ommen, E Bakker, M Burmeister, P L Pearson.   

Abstract

We have isolated 70kb of sequences surrounding probe 754 (DXS84), linked with Duchenne muscular dystrophy. In addition to the original PstI RFLP detected by 754, BglII and EcoRI RFLPs were detected with the single copy subclone 754.11 and a HindIII RFLP with the subclone 754.6. The BglII and HindIII and HindIII RFLPs both have minor allele frequencies of 40%, as in PstI polymorphism. The EcoRI polymorphism has a minor allele frequency of 23%. Since a linkage disequilbrium is observed between these RFLPs (P less than 0.001), the BglII and the HindIII RFLPs do not contribute to the heterozygosity. However, the minor allele of the EcoRI RFLP segregates exclusively with the major haplotype of the PstI-BglII-HindIII complex, and consequently 47% of the homozygotes for the haplotype become heterozygous. As a result, the overall heterozygote frequency of the DXS84 locus increases from 50% to 65%.

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Year:  1986        PMID: 2877935     DOI: 10.1007/bf00282547

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


  17 in total

1.  Complex glycerol kinase deficiency syndrome explained as X-chromosomal deletion.

Authors:  B Wieringa; T Hustinx; J Scheres; W Renier; B ter Haar
Journal:  Clin Genet       Date:  1985-05       Impact factor: 4.438

2.  Analysis of cosmids using linearization by phage lambda terminase.

Authors:  H R Rackwitz; G Zehetner; H Murialdo; H Delius; J H Chai; A Poustka; A Frischauf; H Lehrach
Journal:  Gene       Date:  1985       Impact factor: 3.688

3.  Selective isolation of cosmid clones by homologous recombination in Escherichia coli.

Authors:  A Poustka; H R Rackwitz; A M Frischauf; B Hohn; H Lehrach
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

4.  Separation of chromosomal DNA molecules from yeast by orthogonal-field-alternation gel electrophoresis.

Authors:  G F Carle; M V Olson
Journal:  Nucleic Acids Res       Date:  1984-07-25       Impact factor: 16.971

5.  Plasmid screening at high colony density.

Authors:  D Hanahan; M Meselson
Journal:  Gene       Date:  1980-06       Impact factor: 3.688

6.  Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.

Authors:  M H Hofker; M C Wapenaar; N Goor; E Bakker; G J van Ommen; P L Pearson
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

7.  Separation of yeast chromosome-sized DNAs by pulsed field gradient gel electrophoresis.

Authors:  D C Schwartz; C R Cantor
Journal:  Cell       Date:  1984-05       Impact factor: 41.582

8.  Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Authors:  U Francke; H D Ochs; B de Martinville; J Giacalone; V Lindgren; C Distèche; R A Pagon; M H Hofker; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

9.  Isolation of a random cosmid clone, cX5, which defines a new polymorphic locus DXS148 near the locus for Duchenne muscular dystrophy.

Authors:  M H Hofker; A A Bergen; M I Skraastad; E Bakker; U Francke; B Wieringa; J Bartley; G J van Ommen; P L Pearson
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

10.  DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Authors:  E Bakker; E J Bonten; L F De Lange; H Veenema; D Majoor-Krakauer; M H Hofker; G J Van Ommen; P L Pearson
Journal:  J Med Genet       Date:  1986-12       Impact factor: 6.318

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  19 in total

1.  Molecular analysis of aberrations of Xp and Yq.

Authors:  S D Cheng; R Gasparini; U Müller
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132

2.  Nance-Horan syndrome: localization within the region Xp21.1-Xp22.3 by linkage analysis.

Authors:  D Stambolian; R A Lewis; K Buetow; A Bond; R Nussbaum
Journal:  Am J Hum Genet       Date:  1990-07       Impact factor: 11.025

3.  Complete physical map of the human immunoglobulin heavy chain constant region gene complex.

Authors:  M H Hofker; M A Walter; D W Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1989-07       Impact factor: 11.205

4.  Physical linkage of a human immunoglobulin heavy chain variable region gene segment to diversity and joining region elements.

Authors:  H W Schroeder; M A Walter; M H Hofker; A Ebens; K Willems van Dijk; L C Liao; D W Cox; E C Milner; R M Perlmutter
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

5.  Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardation.

Authors:  M H Hofker; A A Bergen; M I Skraastad; N J Carpenter; H Veenema; J M Connor; E Bakker; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1987-04       Impact factor: 11.025

6.  Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.

Authors:  S E Bodrug; J R Roberson; L Weiss; P N Ray; R G Worton; D L Van Dyke
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

7.  Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.

Authors:  N T Bech-Hansen; W G Pearce
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

8.  Deficient repair of the transcribed strand of active genes in Cockayne's syndrome cells.

Authors:  A van Hoffen; A T Natarajan; L V Mayne; A A van Zeeland; L H Mullenders; J Venema
Journal:  Nucleic Acids Res       Date:  1993-12-25       Impact factor: 16.971

9.  The genetic defect in Cockayne syndrome is associated with a defect in repair of UV-induced DNA damage in transcriptionally active DNA.

Authors:  J Venema; L H Mullenders; A T Natarajan; A A van Zeeland; L V Mayne
Journal:  Proc Natl Acad Sci U S A       Date:  1990-06       Impact factor: 11.205

10.  Immunohistochemical studies show truncated dystrophins in the myotubes of three fetuses at risk for Duchenne muscular dystrophy.

Authors:  I B Ginjaar; E Bakker; M M van Paassen; J T den Dunnen; A Wessels; E E Zubrzycka-Gaarn; A F Moorman; G J van Ommen
Journal:  J Med Genet       Date:  1991-08       Impact factor: 6.318

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