Literature DB >> 7726164

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

M Wijker1, 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.   

Abstract

Bullous dystrophy, hereditary macular type (McKusick 302000), is an X-linked disorder and was originally described in a single kindred in the Netherlands by Mendes da Costa and Van der Valk in 1908. To determine the location of the bullous dystrophy gene, segregation studies were performed in this family and in a recently described Italian family. Using informative polymorphic markers, the gene could initially be localized on the Xq27-q28 region. No recombinants were noted with loci in Xq27.3-q28. Fine mapping places the bullous dystrophy locus distal to DXS102 (Xq26.3) in the Italian family and distal to DXS998 (Xq27.3) in the Dutch family.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7726164      PMCID: PMC1801474     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  12 in total

1.  Rapid PCR analysis of the St14 (DXS52) VNTR.

Authors:  B Richards; R Heilig; I Oberlé; L Storjohann; G T Horn
Journal:  Nucleic Acids Res       Date:  1991-04-25       Impact factor: 16.971

2.  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

Review 3.  Hereditary epidermolysis bullosa.

Authors:  R M Haber; W Hanna; C A Ramsay; L B Boxall
Journal:  J Am Acad Dermatol       Date:  1985-08       Impact factor: 11.527

4.  Report and abstracts of the Fourth International Workshop on Human X Chromosome Mapping 1993. St. Louis, Missouri, May 9-12, 1993.

Authors:  D Schlessinger; J L Mandel; A P Monaco; D L Nelson; H F Willard
Journal:  Cytogenet Cell Genet       Date:  1993

5.  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

6.  Dystrophia bullosa hereditaria, typus maculatus (Mendes da Costa-van der Valk): a rare genodermatosis [proceedings].

Authors:  J H Hassing; H M Doeglas
Journal:  Br J Dermatol       Date:  1980-04       Impact factor: 9.302

7.  Easy calculations of lod scores and genetic risks on small computers.

Authors:  G M Lathrop; J M Lalouel
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

8.  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

Review 9.  X-linked mental retardation, microcephaly, and growth delay associated with hereditary bullous dystrophy macular type: report of a second family.

Authors:  M S Lungarotti; C Martello; G Barboni; D Mezzetti; G Mariotti; A Calabro
Journal:  Am J Med Genet       Date:  1994-07-15

10.  Human biglycan gene. Putative promoter, intron-exon junctions, and chromosomal localization.

Authors:  L W Fisher; A M Heegaard; U Vetter; W Vogel; W Just; J D Termine; M F Young
Journal:  J Biol Chem       Date:  1991-08-05       Impact factor: 5.157

View more
  1 in total

1.  X linked severe mental retardation, craniofacial dysmorphology, epilepsy, ophthalmoplegia, and cerebellar atrophy in a large South African kindred is localised to Xq24-q27.

Authors:  A L Christianson; R E Stevenson; C H van der Meyden; J Pelser; F W Theron; P L van Rensburg; M Chandler; C E Schwartz
Journal:  J Med Genet       Date:  1999-10       Impact factor: 6.318

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.