Found: 23
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Genetic Control of Serum IgE Levels and Asthma: Linkage and Linkage Disequilibrium Studies in an Isolated Population.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2069, doi. 10.1093/hmg/6.12.2069
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- Article
Isolation of a Candidate Human Telomerase Catalytic Subunit Gene, Which Reveals Complex Splicing Patterns in Different Cell Types.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2011, doi. 10.1093/hmg/6.12.2011
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- Article
Recurrent Mutations in a Single Exon Encoding the Evolutionarily Conserved Olfactomedin-Homology Domain of TIGR in Familial Open-Angle Glaucoma.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2091, doi. 10.1093/hmg/6.12.2091
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- Article
Evidence for Uniparental, Paternal Expression of the Human GABAA Receptor Subunit Genes, Using Microcell-Mediated Chromosome Transfer.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2127, doi. 10.1093/hmg/6.12.2127
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- Article
Distortion of Allelic Expression of Apolipoprotein E in Alzheimer's Disease.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2151, doi. 10.1093/hmg/6.12.2151
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- Article
Rethinking Genotype and Phenotype Correlations in Polyglutamine Expansion Disorders.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2005, doi. 10.1093/hmg/6.12.2005
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- Article
Aberrant Processing of the Fugu HD (FrHD) mRNA in Mouse Cells and in Transgenic Mice.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2141, doi. 10.1093/hmg/6.12.2141
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- Article
A New Pathogenic Mutation in the APP Gene (I716V) Increases the Relative Proportion of Aβ42(43).
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2087, doi. 10.1093/hmg/6.12.2087
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- Publication type:
- Article
Molecular Genetic and Phenotypic Analysis Reveals Differences between TSC1 and TSC2 Associated Familial and Sporadic Tuberous Sclerosis.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2155, doi. 10.1093/hmg/6.12.2155
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- Article
Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2173, doi. 10.1093/hmg/6.12.2173
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- Article
Genetic Susceptibility for Human Familial Essential Hypertension in a Region of Homology with Blood Pressure Linkage on Rat Chromosome 10.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2077, doi. 10.1093/hmg/6.12.2077
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- Publication type:
- Article
cDNA Cloning and Chromosomal mapping of a Predicted Coiled-Coil Proline-Rich Protein Immunogenic in Meningioma Patients.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2031, doi. 10.1093/hmg/6.12.2031
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- Publication type:
- Article
IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2179, doi. 10.1093/hmg/6.12.2179
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- Article
Isolation of a New Homeobox Gene Belonging to the Pitx/Rieg Family: Expression During Lens Development and Mapping to the Aphakia Region on Mouse Chromosome 19.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2109, doi. 10.1093/hmg/6.12.2109
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- Article
Germline Mutations of the CDKN2 Gene in UK Melanoma Families.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2061, doi. 10.1093/hmg/6.12.2061
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- Article
Increased Trinucleotide Repeat Instability with Advanced Maternal Age.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2135, doi. 10.1093/hmg/6.12.2135
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- Article
The Human GARS-AIRS-GART Gene Encodes Two Proteins Which Are Differentially Expressed during Human Brain Development and Temporally Overexpressed in Cerebellum of Individuals with Down Dyndrome.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2043, doi. 10.1093/hmg/6.12.2043
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- Article
Mammalian Telomerase: Catalytic Subunit and Knockout Mice.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 1999, doi. 10.1093/hmg/6.12.1999
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- Article
Higher Proportion of Intact Exon 9 CFTR mRNA in Nasal Epithelium Compared with Vas Deferens.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2099, doi. 10.1093/hmg/6.12.2099
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- Publication type:
- Article
Two Different Connexin 26 Mutations in an Inbred Kindred Segregating Non-Syndromic Recessive Deafness: Implications for Genetic Studies in Isolated Populations.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2163, doi. 10.1093/hmg/6.12.2163
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- Publication type:
- Article
The IPL Gene on Chromosome 11p15.5 is Imprinted in Humans and Mice and is Similar to TDAG51, Implicated in Fas Expression and Apoptosis.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2021, doi. 10.1093/hmg/6.12.2021
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- Article
Identification and Characterization of Human Genes Encoding Hprp3p and Hprp4p, Interacting Components of the Spliceosome.
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- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2117, doi. 10.1093/hmg/6.12.2117
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- Article
Structural and Functional Characterization of the Human FMR1 Promoter Reveals Similarities with the hnRNP-A2 Promoter Region.
- Published in:
- Human Molecular Genetics, 1997, v. 6, n. 12, p. 2051, doi. 10.1093/hmg/6.12.2051
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- Publication type:
- Article