Literature DB >> 1847690

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

A Sefiani1, R M'rad, L Simard, A Vincent, C Julier, L Holvoet-Vermaut, S Heuertz, N Dahl, J F Stalder, M O Peter.   

Abstract

Linkage data for familial incontinentia pigmenti (IP2) and nine X chromosomal markers are reported. Previously found linkage between IP2 and the DXS52 locus is confirmed with the maximum lod score of 6.19 at a recombination fraction of 0.03. Linkage is also established with loci DXS134, DXS15 and DXS33. Multipoint analysis allows us to localize the IP2 locus outside a block of seven linked markers of the Xq28 region.

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Year:  1991        PMID： 1847690     DOI： 10.1007/bf00202414

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


  13 in total

1.  Incontinentia pigmenti.

Authors:  T Iancu; L Komlos; F Shabtay; E Elian; L Halbrecht; J A Böök
Journal:  Clin Genet       Date:  1975-02       Impact factor: 4.438

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

Authors:  A Vincent; C Kretz; I Oberlé; J L Mandel
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

3.  A polymorphic locus at Xq27-28 detected by the probe U6.2 [DXS304].

Authors:  N Dahl; K Hammarström-Heeroma; G B van Ommen; U Pettersson
Journal:  Nucleic Acids Res       Date:  1989-04-11       Impact factor: 16.971

4.  Report of the Committee on Methods of Linkage Analysis and Reporting.

Authors:  P M Conneally; J H Edwards; K K Kidd; J M Lalouel; N E Morton; J Ott; R White
Journal:  Cytogenet Cell Genet       Date:  1985

5.  Improved DNA markers for efficient analysis of fragile X families.

Authors:  R Heilig; I Oberlé; B Arveiler; A Hanauer; M Vidaud; J L Mandel
Journal:  Am J Med Genet       Date:  1988 May-Jun

6.  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

7.  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

8.  Incontinentia pigmenti: Xp breakpoint is not the same in a case of r(X) and in X/autosome translocations.

Authors:  A Sefiani; S Heuertz; C Turleau; D Thibaud; J de Grouchy; M C Hors-Cayla
Journal:  Ann Genet       Date:  1989

9.  Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11.

Authors:  A Sefiani; D Sinnett; L Abel; S Szpiro-Tapia; S Heuertz; I Craig; N Fraser; T A Kruse; M Frydman; M O Peter
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

10.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205
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  9 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Authors:  T A Angel; C J Faust; J C Gonzales; S Kenwrick; R A Lewis; G E Herman
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

3.  Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmenti.

Authors:  S Das; A Metzenberg; G S Pai; J Gitschier
Journal:  Am J Hum Genet       Date:  1994-05       Impact factor: 11.025

4.  Three patients with ring (X) chromosomes and a severe phenotype.

Authors:  N R Dennis; A L Collins; J A Crolla; A E Cockwell; A M Fisher; P A Jacobs
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

Review 5.  Incontinentia pigmenti nomenclature.

Authors:  V P Sybert
Journal:  Am J Hum Genet       Date:  1994-07       Impact factor: 11.025

6.  De novo mutation in three families with multigenerational incontinentia pigmenti.

Authors:  A Scheuerle; R A Lewis; M L Levy; D L Nelson
Journal:  Am J Hum Genet       Date:  1994-12       Impact factor: 11.025

7.  Interaction of incontinentia pigmenti and factor VIII mutations in a female with biased X inactivation, resulting in haemophilia.

Authors:  R Coleman; S A Genet; J I Harper; A O Wilkie
Journal:  J Med Genet       Date:  1993-06       Impact factor: 6.318

8.  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

9.  The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

Authors:  M Wijker; M J Ligtenberg; F Schoute; J C Defesche; G Pals; P A Bolhuis; H H Ropers; T J Hulsebos; F H Menko; B A van Oost
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025
  9 in total

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