The Wiskott-Aldrich syndrome: refinement of the localization on Xp and identification of another closely linked marker locus, OATL1

[1]  J. Puck,et al.  The gene encoding human TFE3, a transcription factor that binds the immunoglobulin heavy-chain enhancer, maps to Xp11.22. , 1991, Genomics.

[2]  H. Willard,et al.  An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders. , 1991, Genomics.

[3]  H. Willard,et al.  A highly polymorphic dinucleotide repeat on the proximal short arm of the human X chromosome: linkage mapping of the synapsin I/A-raf-1 genes. , 1991, American journal of human genetics.

[4]  J. Ott,et al.  Localization of the gene for the Wiskott-Aldrich syndrome between two flanking markers, TIMP and DXS255, on Xp11.22-Xp11.3. , 1991, Genomics.

[5]  H. Willard,et al.  Ornithine aminotransferase-related sequences map to two nonadjacent intervals on the human X chromosome short arm. , 1991, Genomics.

[6]  J. Dennis,et al.  Aberrant O-linked oligosaccharide biosynthesis in lymphocytes and platelets from patients with the Wiskott-Aldrich syndrome. , 1991, The Journal of biological chemistry.

[7]  K. Siminovitch,et al.  Linkage relationships of the Wiskott-Aldrich syndrome to 10 loci in the pericentromeric region of the human X chromosome. , 1990, Genomics.

[8]  H. Willard,et al.  Linkage studies of the Wiskott-Aldrich syndrome: polymorphisms at TIMP and the X chromosome centromere are informative markers for genetic prediction , 1989, Human Genetics.

[9]  J. Dennis,et al.  Altered expression of leucocyte sialoglycoprotein in Wiskott-Aldrich syndrome is associated with a specific defect in O-glycosylation. , 1989, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[10]  D. Page,et al.  Genetic mapping of the Wiskott-Aldrich syndrome with two highly-linked polymorphic DNA markers. , 1988, Genomics.

[11]  H. Willard,et al.  A primary genetic map of the pericentromeric region of the human X chromosome. , 1988, Genomics.

[12]  D. J. Barrett,et al.  Chromosomal localization of human ornithine aminotransferase gene sequences to 10q26 and Xp11.2. , 1987, Investigative ophthalmology & visual science.

[13]  R. Eddy,et al.  Localization of the ornithine aminotransferase gene and related sequences on two human chromosomes , 1987, Human Genetics.

[14]  K. Siminovitch,et al.  Linkage of the Wiskott-Aldrich syndrome with polymorphic DNA sequences from the human X chromosome. , 1987, Proceedings of the National Academy of Sciences of the United States of America.

[15]  J. Gusella,et al.  Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase. , 1986, DNA.

[16]  J. Mandel,et al.  The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979). , 1980, The Journal of pediatrics.

[17]  J. Ott.  Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. , 1974, American journal of human genetics.

[18]  M. Cooper,et al.  Wiskott-Aldrich syndrome: An immunologic deficiency disease involving the afferent limb of immunity , 1968 .

[19]  D. C. Campbell,et al.  Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. , 1954, Pediatrics.

[20]  Aldrich Ra,et al.  Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea. , 1954 .

[21]  G. Lathrop,et al.  Construction of human linkage maps: Likelihood calculations for multilocus linkage analysis , 1986, Genetic epidemiology.