JOHN BELMONT to X Chromosome
This is a "connection" page, showing publications JOHN BELMONT has written about X Chromosome.
Connection Strength
0.874
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Genetic control of X inactivation and processes leading to X-inactivation skewing. Am J Hum Genet. 1996 Jun; 58(6):1101-8.
Score: 0.123
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Insights into lymphocyte development from X-linked immune deficiencies. Trends Genet. 1995 Mar; 11(3):112-6.
Score: 0.113
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Application of carrier testing to genetic counseling for X-linked agammaglobulinemia. Am J Hum Genet. 1994 Jan; 54(1):25-35.
Score: 0.104
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Trinucleotide repeat polymorphism at DXS101. Hum Mol Genet. 1993 Sep; 2(9):1508.
Score: 0.102
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Dinucleotide repeat polymorphism in the human CD40 ligand gene. Hum Mol Genet. 1993 Jun; 2(6):828.
Score: 0.100
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Dinucleotide repeat polymorphism at the DXS178 locus. Hum Mol Genet. 1992 Jun; 1(3):216.
Score: 0.093
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A single strand conformation polymorphism study of CD40 ligand. Efficient mutation analysis and carrier detection for X-linked hyper IgM syndrome. J Clin Invest. 1996 Jan 01; 97(1):196-201.
Score: 0.030
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Sixty-nine kilobases of contiguous human genomic sequence containing the alpha-galactosidase A and Bruton's tyrosine kinase loci. Mamm Genome. 1995 May; 6(5):334-8.
Score: 0.029
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Mild phenotypic effects of a de novo deletion Xpter-->Xp22.3 and duplication 3pter-->3p23. Am J Med Genet. 1995 Mar 13; 56(1):16-21.
Score: 0.028
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Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase elk to a 200-kilobasepair region in human chromosome Xq12. Genomics. 1995 Jan 01; 25(1):334-5.
Score: 0.028
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Parental origin of the extra chromosomes in polysomy X. Hum Genet. 1994 Oct; 94(4):423-6.
Score: 0.027
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The genomic structure of human BTK, the defective gene in X-linked agammaglobulinemia. Immunogenetics. 1994; 40(5):319-24.
Score: 0.026
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The biology of the human ligand for CD40. J Clin Immunol. 1993 Nov; 13(6):373-80.
Score: 0.026
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Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22. Genomics. 1993 Feb; 15(2):342-9.
Score: 0.024
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A complex syndrome of left-right axis, central nervous system and axial skeleton defects in Zic3 mutant mice. Development. 2002 May; 129(9):2293-302.
Score: 0.012
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Further associations of congenital heart disease and genetic syndromes: report of a case of tetralogy of Fallot and Fabry's disease. Pediatr Cardiol. 1999 May-Jun; 20(3):236-7.
Score: 0.009