Works matching IS 14345161 AND DT 2002 AND VI 47 AND IP 5
Results: 10
Variability of the human aryl hydrocarbon receptor nuclear translocator (ARNT) gene.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 217, doi. 10.1007/s100380200028
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Identification of lamin A/C (LMNA) gene mutations in Korean patients with autosomal dominant Emery-Dreifuss muscular dystrophy and limb-girdle muscular dystrophy 1B.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 225, doi. 10.1007/s100380200029
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Novel missense mutation (R94S) in the TAZ (G4.5) gene in a Japanese patient with Barth syndrome.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 229
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Allelic structures at hypervariable minisatellite B6.7 in Japanese show population specificity.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 232, doi. 10.1007/s100380200031
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The CpG island in intron 22 of the factor VIII gene is predominantly methylated on the X chromosome of human males.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 239, doi. 10.1007/s100380200032
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Association of a polymorphism of the transforming growth factor-β1 gene with blood pressure in Japanese individuals.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 243, doi. 10.1007/s100380200033
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Contribution of Sp1 to initiation of transcription of angiotensinogen.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 249, doi. 10.1007/s100380200034
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Microdeletions of a Y-specific marker, Yfm1, and implications for a role in spermatogenesis.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 257, doi. 10.1007/s100380200035
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Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 262, doi. 10.1007/s100380200036
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A novel human gene whose product shares homology with bovine brain-specific protein p25 is expressed in fetal brain but not in adult brain.
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- Journal of Human Genetics, 2002, v. 47, n. 5, p. 266, doi. 10.1007/s100380200037
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- Article