Literature DB >> 2906042

Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers.

S P Kwan1, L A Sandkuyl, M Blaese, L M Kunkel, G Bruns, R Parmley, S Skarshaug, D C Page, J Ott, F S Rosen.   

Abstract

The Wiskott-Aldrich syndrome (WAS) is an X-linked recessive genetic disease in which the molecular defect is unknown. In 15 families with WAS, seven restriction fragment length polymorphic loci from the X chromosome were used to map the disease locus. Of the eight intervals studied, the likelihood of the WAS gene lying between DXS7 (Xp11.3) and DXS14 (Xp11) was at least 128 times higher than that for any other interval. The most likely gene order is DXS84-OTC-DXS7-WAS-DXS14-DXS1-PGK-DXYS1. Close genetic linkage to DXS7 and DXS14 permits accurate prenatal diagnosis and carrier detection with greater than 98% confidence in fully informative WAS families.

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Year:  1988        PMID: 2906042     DOI: 10.1016/0888-7543(88)90156-5

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  15 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Germ-line mosaicism simulates genetic heterogeneity in Wiskott-Aldrich syndrome.

Authors:  B Arveiler; G de Saint-Basile; A Fischer; C Griscelli; J L Mandel
Journal:  Am J Hum Genet       Date:  1990-05       Impact factor: 11.025

Review 4.  The Wiskott-Aldrich syndrome.

Authors:  H D Ochs
Journal:  Springer Semin Immunopathol       Date:  1998

5.  Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction.

Authors:  W L Greer; M M Mahtani; P C Kwong; L A Rubin; M Peacocke; H F Willard; K A Siminovitch
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

6.  Haplotype and multipoint linkage analysis in Finnish choroideremia families.

Authors:  E M Sankila; T Lehner; A W Eriksson; H Forsius; J Kärnä; D Page; J Ott; A de la Chapelle
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

7.  Analysis of X-chromosome inactivation and presumptive expression of the Wiskott-Aldrich syndrome (WAS) gene in hematopoietic cell lineages of a thrombocytopenic carrier female of WAS.

Authors:  L D Notarangelo; O Parolini; F Porta; F Locatelli; A Lanfranchi; M Marconi; L Nespoli; A Albertini; I W Craig; A G Ugazio
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

8.  Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene.

Authors:  S P Kwan; T L Hagemann; B E Radtke; R M Blaese; F S Rosen
Journal:  Proc Natl Acad Sci U S A       Date:  1995-05-09       Impact factor: 11.205

9.  Linkage of Wiskott-Aldrich syndrome with three marker loci, DXS426, SYP and TFE3, which map to the Xp11.3-p11.22 region.

Authors:  S M Cremin; W L Greer; R Bodok-Nutzati; M Schwartz; M Peacocke; K A Siminovitch
Journal:  Hum Genet       Date:  1993-10-01       Impact factor: 4.132

10.  Addison disease 10 years after bone marrow transplantation for Wiskott-Aldrich syndrome.

Authors:  B Latal Hajnal; U Lips; W Friedrich; M Zachmann; F Berthet
Journal:  Eur J Pediatr       Date:  1995-09       Impact factor: 3.183

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