Works matching IS 14345161 AND DT 1998 AND VI 43 AND IP 1
Results: 16
Human autoimmune lymphoproliferative syndrome, a defect in the apoptosis-inducing Fas receptor: A lesson from the mouse model.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 2, doi. 10.1007/s100380050029
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Identification by differential display of eight known genes induced during in vivo intimal hyperplasia.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 9, doi. 10.1007/s100380050030
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An HLA-binding-motif-aided peptide epitope library: A novel library design for the screening of HLA-DR4-restricted antigenic peptides recognized by CD4[sup +] T cells.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 14, doi. 10.1007/s100380050031
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Refinement of the gene locus for autosomal recessive juvenile parkinsonism (AR-JP) on chromosome 6q25.2-27 and identification of markers exhibiting linkage disequilibrium.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 22, doi. 10.1007/s100380050032
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The gene for mesomelic dysplasia Kantaputra type is mapped to chromosome 2q24-q32.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 32, doi. 10.1007/s100380050033
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-6A Promoter variant of angiotensinogen and blood pressure variation in Canadian Oji-Cree.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 37, doi. 10.1007/s100380050034
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High proportion of missense mutations of the BRCA1 and BRCA2 genes in Japanese breast cancer families.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 42, doi. 10.1007/s100380050035
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In situ detection of insulin-like growth factor II (IGF2) and H19 gene expression in hepatocellular carcinoma.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 49, doi. 10.1007/s100380050036
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Expression analysis of two mutant human ornithine transcarbamylases in COS-7 cells.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 54, doi. 10.1007/s100380050037
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New radiological finding by magnetic resonance imaging examination of the brain in Coffin-Lowry syndrome.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 59, doi. 10.1007/s100380050038
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A severe case of Moebius syndrome with calcification on the fourth ventricular floor.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 62, doi. 10.1007/s100380050039
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A case of craniofacial dysmorphism, congenital heart defects, coccygeal skin folds, generalized skeletal alterations, and hemihypertrophy with linear skin hypopigmentation: A new syndrome?
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 65, doi. 10.1007/s100380050040
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A SacII polymorphism in the human ASCL2 (HASH2) gene region.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 69, doi. 10.1007/s100380050041
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Isolation and mapping of a polymorphic CA repeat sequence at the human interleukin 6 locus.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 71, doi. 10.1007/s100380050042
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Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human estrogen receptor β locus.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 73, doi. 10.1007/s100380050043
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Isolation and radiation hybrid mapping of dinucleotide repeat polymorphism at the human matrix Gla protein (MGP) locus.
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- Journal of Human Genetics, 1998, v. 43, n. 1, p. 75, doi. 10.1007/s100380050044
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