Literature DB >> 2565870

A new polymorphic marker very closely linked to DXS52 in the q28 region of the human X chromosome.

A Vincent1, C Kretz, I Oberlé, J L Mandel.   

Abstract

We have isolated an X chromosome probe, St35.691 (DXS305), which detects two RFLPs with TaqI and PstI, whose combined heterozygosity is about 60%. This probe has been assigned to Xq28 by physical and genetic mapping and is very closely linked to DXS52, DXS15, and the coagulation factor VIII gene (F8C). The best estimate of the recombination fraction for the DXS52-DXS305 interval is 0.014, with a lod score of 50.1. Multipoint analysis places DXS305 on the same side of F8C as DXS52, but complete ordering of the three loci was not possible with our present data. This highly informative marker should be useful in the precise mapping of the many disease genes that have been assigned to the Xq28 band.

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Year:  1989        PMID： 2565870     DOI： 10.1007/BF00288280

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


  8 in total

1.  The gene for incontinentia pigmenti is assigned to Xq28.

Authors:  A Sefiani; L Abel; S Heuertz; D Sinnett; L Lavergne; D Labuda; M C Hors-Cayla
Journal:  Genomics       Date:  1989-04       Impact factor: 5.736

2.  Report of the committee on the genetic constitution of the X and Y chromosomes.

Authors:  K E Davies; J L Mandel; J Weissenbach; M Fellous
Journal:  Cytogenet Cell Genet       Date:  1987

3.  Genetic mapping of the Xq27-q28 region: new RFLP markers useful for diagnostic applications in fragile-X and hemophilia-B families.

Authors:  B Arveiler; I Oberlé; A Vincent; M H Hofker; P L Pearson; J L Mandel
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

4.  Mapping of DNA markers close to the fragile site on the human X chromosome at Xq27.3.

Authors:  M Patterson; S Kenwrick; S Thibodeau; K Faulk; M G Mattei; J F Mattei; K E Davies
Journal:  Nucleic Acids Res       Date:  1987-03-25       Impact factor: 16.971

Review 5.  From hemophilia B to hemophilia A via the fragile X locus: genes and recombination in the distal region of the human X chromosome long arm.

Authors:  I Oberlé; J L Mandel
Journal:  Horiz Biochem Biophys       Date:  1986

6.  Toward a physical map of the Xq28 region in man: linking color vision, G6PD, and coagulation factor VIII genes to an X-Y homology region.

Authors:  B Arveiler; A Vincent; J L Mandel
Journal:  Genomics       Date:  1989-05       Impact factor: 5.736

7.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Am J Hum Genet       Date:  1985-05       Impact factor: 11.025

8.  Physical mapping studies on the human X chromosome in the region Xq27-Xqter.

Authors:  M Patterson; C Schwartz; M Bell; S Sauer; M Hofker; B Trask; G van den Engh; K E Davies
Journal:  Genomics       Date:  1987-12       Impact factor: 5.736
  8 in total
  13 in total

1.  Fried syndrome is a distinct X linked mental retardation syndrome mapping to Xp22.

Authors:  L Strain; A F Wright; D T Bonthron
Journal:  J Med Genet       Date:  1997-07       Impact factor: 6.318

2.  Microdissection of the fragile X region.

Authors:  R N MacKinnon; M C Hirst; M V Bell; J E Watson; U Claussen; H J Ludecke; G Senger; B Horsthemke; K E Davies
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

3.  Physical linkage of a GABAA receptor subunit gene to the DXS374 locus in human Xq28.

Authors:  M V Bell; J Bloomfield; M McKinley; M N Patterson; M G Darlison; E A Barnard; K E Davies
Journal:  Am J Hum Genet       Date:  1989-12       Impact factor: 11.025

4.  Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers.

Authors:  A Sefiani; R M'rad; L Simard; A Vincent; C Julier; L Holvoet-Vermaut; S Heuertz; N Dahl; J F Stalder; M O Peter
Journal:  Hum Genet       Date:  1991-01       Impact factor: 4.132

5.  X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies.

Authors:  D G Bichet; G N Hendy; M Lonergan; M F Arthus; S Ligier; Z Pausova; R Kluge; H Zingg; P Saenger; E Oppenheimer
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

6.  Physical map of human Xq27-qter: localizing the region of the fragile X mutation.

Authors:  A Poustka; A Dietrich; G Langenstein; D Toniolo; S T Warren; H Lehrach
Journal:  Proc Natl Acad Sci U S A       Date:  1991-10-01       Impact factor: 11.205

7.  Three Finnish incontinentia pigmenti (IP) families with recombinations with the IP loci at Xq28 and Xp11.

Authors:  C Hydén-Granskog; R Salonen; H von Koskull
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

8.  X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).

Authors:  N Dahl; F Samson; N S Thomas; L J Hu; W Gong; G Herman; J Laporte; P Kioschis; A Poustka; J L Mandel
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

9.  Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.

Authors:  V Biancalana; B Le Marec; S Odent; J A van den Hurk; A Hanauer
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

10.  Myotubular myopathy in a girl with a deletion at Xq27-q28 and unbalanced X inactivation assigns the MTM1 gene to a 600-kb region.

Authors:  N Dahl; L J Hu; M Chery; M Fardeau; S Gilgenkrantz; A Nivelon-Chevallier; I Sidaner-Noisette; F Mugneret; J B Gouyon; A Gal
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025
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