Literature DB >> 3192215

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

A Sefiani1, D Sinnett, L Abel, S Szpiro-Tapia, S Heuertz, I Craig, N Fraser, T A Kruse, M Frydman, M O Peter.   

Abstract

Linkage studies have been performed in 5 incontinentia pigmenti (IP) families totaling 29 potentially informative meioses. Ten probes of the Xp arm were used, six of them were precisely localized on the X chromosome, using hamster X human somatic cell hybrids containing a broken X chromosome derived from an incontinentia pigmenti patient carrying an X;9 translocation [46,XX,t(X;9)(p11.21;q34)]. The following order for probes is proposed: pter - (DXS7, DXS146, DXS255) - IP1 - (DXS14, DXS90) - DXS106 - qter. The negative lod scores obtained exclude the possibility that in the families studied, the gene for IP is located in Xp11 or in the major part of the Xp arm.

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Year:  1988        PMID： 3192215     DOI： 10.1007/bf01790098

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


  23 in total

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Journal:  Nucleic Acids Res       Date:  1986-02-25       Impact factor: 16.971

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Journal:  Proc Natl Acad Sci U S A       Date:  1977-03       Impact factor: 11.205

Review 5.  Investigation of genetic linkage in human families.

Authors:  R White; J M Lalouel
Journal:  Adv Hum Genet       Date:  1987

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Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

7.  Two cases of X/autosome translocation in females with incontinentia pigmenti.

Authors:  S V Hodgson; B Neville; R W Jones; C Fear; M Bobrow
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Gene for incontinentia pigmenti maps to band Xp11 with an (X;10) (p11;q22) translocation.

Authors:  L A Cannizzaro; F Hecht
Journal:  Clin Genet       Date:  1987-07       Impact factor: 4.438

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Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
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10.  Loss of human genetic markers in man--Chinese hamster somatic cell hybrids.

Authors:  A Westerveld; R P Visser; P Meera Khan; D Bootsma
Journal:  Nat New Biol       Date:  1971-11-03
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  12 in total

1.  X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.

Authors:  A Harris; J Collins; D Vetrie; C Cole; M Bobrow
Journal:  J Med Genet       Date:  1992-09       Impact factor: 6.318

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

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

Review 3.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

Review 4.  Mapping dysmorphic syndromes with the aid of the human/mouse homology map.

Authors:  R P Erickson
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

Review 5.  Hypomelanosis of Ito and X;autosome translocations: a unifying hypothesis.

Authors:  E Hatchwell
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

6.  X inactivation analysis in a female with hypomelanosis of Ito associated with a balanced X;17 translocation: evidence for functional disomy of Xp.

Authors:  E Hatchwell; D Robinson; J A Crolla; A E Cockwell
Journal:  J Med Genet       Date:  1996-03       Impact factor: 6.318

7.  Possible genetic heterogeneity in X linked hypohidrotic ectodermal dysplasia.

Authors:  J Goodship; S Malcolm; A Clarke; M E Pembrey
Journal:  J Med Genet       Date:  1990-07       Impact factor: 6.318

8.  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

9.  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

10.  Partial inversion of gene order within a homologous segment on the X chromosome.

Authors:  S H Laval; Y Boyd
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957
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