Works matching IS 09646906 AND DT 1996 AND VI 5 AND IP 8
Results: 17
Differential Expression of Dystrophin Isoforms in Strains of mdx Mice with Different Mutations.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1149
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- Article
A Second Locus (GLC3B) for Primary Congenital Glaucoma (Buphthalmos) Maps to the 1p36 Region.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1199, doi. 10.1093/hmg/5.8.1199
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- Article
Biallelic Expression of the IGF2 Gene in Human Breast Disease.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1123, doi. 10.1093/hmg/5.8.1123
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- Article
The Kallmann Syndrome Gene Product Expressed in COS Cells is Cleaved on the Cell Surface to Yield a Diffusible Component.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1109, doi. 10.1093/hmg/5.8.1109
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- Article
Chromosomal Stabilisation by a Subtelomeric Rearrangement Involving Two Closely Related Alu Elements.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1163, doi. 10.1093/hmg/5.8.1163
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- Article
Human Usher 1B/Mouse shaker-1: The Retinal Phenotype Discrepancy Explained By The Presence/Absence of Myosin VIIA in The Photoreceptor Cells.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1171, doi. 10.1093/hmg/5.8.1171
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- Article
The Fragile X Mental Retardation Protein is a Ribonucleoprotein Containing Both Nuclear Localization and Nuclear Export Signals.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1083, doi. 10.1093/hmg/5.8.1083
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- Article
Mouse/Human Sequence Divergence in a Region with a Paternal-Specific Methylation Imprint at the Human H19 Locus.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1155, doi. 10.1093/hmg/5.8.1155
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- Article
Identification of a Novel Sarcoglycan Gene at 5q33 Encoding a Sarcolemmal 35 kDa Glycoprotein.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1179, doi. 10.1093/hmg/5.8.1179
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- Article
Further Evidence for an Imprinted Gene for Neonatal Diabetes Localised to Chromosome 6q22–q23.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1117, doi. 10.1093/hmg/5.8.1117
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- Article
Chromosome 11p15.5 Regional Imprinting: Comparative Analysis of KIP2 and H19 in Human Tissues and Wilms' Tumors.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1101, doi. 10.1093/hmg/5.8.1101
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- Article
Association between Atopic Asthma and a Coding Variant of FcεRIβ in a Japanese Population.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1129, doi. 10.1093/hmg/5.8.1129
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- Article
Identification of a New Locus for Autosomal Dominant Non-Syndromic Hearing Impairment (DFNA7) in a Large Norwegian Family.
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- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1187, doi. 10.1093/hmg/5.8.1187
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- Article
A Fine-Scale Comparison of the Human and Chimpanzee Genomes: Linkage, Linkage Disequilibrium and Sequence Analysis.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1131, doi. 10.1093/hmg/5.8.1131
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- Publication type:
- Article
Ott, a Mouse X-Linked Multigene Family Expressed Specifically During Meiosis.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1139, doi. 10.1093/hmg/5.8.1139
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- Article
A Ninth Locus (RP18) for Autosomal Dominant Retinitis Pigmentosa Maps in the Pericentromeric Region of Chromosome 1.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1193
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- Publication type:
- Article
Subcellular Localization of the Huntington's Disease Gene Product in Cell Lines by Immunofluorescence and Biochemical Subcellular Fractionation.
- Published in:
- Human Molecular Genetics, 1996, v. 5, n. 8, p. 1093, doi. 10.1093/hmg/5.8.1093
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- Article