Works matching IS 14345161 AND DT 2003 AND VI 48 AND IP 7
Results: 12
Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 397, doi. 10.1007/s10038-003-0049-8
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STR polymorphisms of "forensic loci" in the northern Han Chinese population.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 337, doi. 10.1007/s10038-003-0034-2
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Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testis.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 393, doi. 10.1007/s10038-003-0033-3
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A mutation analysis of the BRCA1 gene in 140 families from southeast France with a history of breast and/or ovarian cancer.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 362, doi. 10.1007/s10038-003-0038-y
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Leber's hereditary optic neuropathy with 14484 mutation in Central Java, Indonesia.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 385
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Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 352, doi. 10.1007/s10038-003-0037-z
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Complete absence of bile and pancreatic ducts in a newborn: a new entity of congenital anomaly in hepato-pancreatic development.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 380, doi. 10.1007/s10038-003-0041-3
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Linkage analysis suggests a locus of ichthyosis vulgaris on 1q22.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 390, doi. 10.1007/s10038-003-0043-1
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CpG dinucleotide methylation patterns in the human androgen receptor gene and X-chromosome inactivation in peripheral blood leukocytes of phenotypically normal women.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 374, doi. 10.1007/s10038-003-0040-4
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Effect of the factor VII R353Q missense mutation on plasma apolipoprotein B levels: impact of visceral obesity.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 367, doi. 10.1007/s10038-003-0039-x
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Extreme androgen resistance in a kindred with a novel insertion/deletion mutation in exon 5 of the androgen receptor gene.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 346, doi. 10.1007/s10038-003-0036-0
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Association of genetic variation of the RIL gene, encoding a PDZ-LIM domain protein and localized in 5q31.1, with low bone mineral density in adult Japanese women.
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- Journal of Human Genetics, 2003, v. 48, n. 7, p. 342, doi. 10.1007/s10038-003-0035-1
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