Human Molecular Genetics

ARTICLES:

DE Eberhart, HE Malter, Y Feng, and ST Warren

The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals
Hum. Mol. Genet. 1996 5: 1083-1091; doi:10.1093/hmg/5.8.1083 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

KE De Rooij, JC Dorsman, MA Smoor, JT Den Dunnen, and GJ Van Ommen

Subcellular localization of the Huntington's disease gene product in cell lines by immunofluorescence and biochemical subcellular fractionation
Hum. Mol. Genet. 1996 5: 1093-1099; doi:10.1093/hmg/5.8.1093 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

WY Chung, L Yuan, L Feng, T Hensle, and B Tycko

Chromosome 11p15.5 regional imprinting: comparative analysis of KIP2 and H19 in human tissues and Wilms' tumors
Hum. Mol. Genet. 1996 5: 1101-1108; doi:10.1093/hmg/5.8.1101 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

EI Rugarli, C Ghezzi, V Valsecchi, and A Ballabio

The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component
Hum. Mol. Genet. 1996 5: 1109-1115; doi:10.1093/hmg/5.8.1109 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

IK Temple, RJ Gardner, DO Robinson, MS Kibirige, AW Ferguson, JD Baum, JC Barber, RS James, and JP Shield

Further evidence for an imprinted gene for neonatal diabetes localised to chromosome 6q22-q23
Hum. Mol. Genet. 1996 5: 1117-1121; doi:10.1093/hmg/5.8.1117 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

AH McCann, N Miller, A O'Meara, I Pedersen, K Keogh, T Gorey, and PA Dervan

Biallelic expression of the IGF2 gene in human breast disease
Hum. Mol. Genet. 1996 5: 1123-1127; doi:10.1093/hmg/5.8.1123 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

T Shirakawa, XQ Mao, S Sasaki, T Enomoto, M Kawai, K Morimoto, and J Hopkin

Association between atopic asthma and a coding variant of Fc epsilon RI beta in a Japanese population [published erratum appears in Hum Mol Genet 1996 Dec;5(12):2068]
Hum. Mol. Genet. 1996 5: 1129-1130; doi:10.1093/hmg/5.8.1129 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

B Crouau-Roy, S Service, M Slatkin, and N Freimer

A fine-scale comparison of the human and chimpanzee genomes: linkage, linkage disequilibrium and sequence analysis
Hum. Mol. Genet. 1996 5: 1131-1137; doi:10.1093/hmg/5.8.1131 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

SM Kerr, MH Taggart, M Lee, and HJ Cooke

Ott, a mouse X-linked multigene family expressed specifically during meiosis
Hum. Mol. Genet. 1996 5: 1139-1148; doi:10.1093/hmg/5.8.1139 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

WB Im, SF Phelps, EH Copen, EG Adams, JL Slightom, and JS Chamberlain

Differential expression of dystrophin isoforms in strains of mdx mice with different mutations
Hum. Mol. Genet. 1996 5: 1149-1153; doi:10.1093/hmg/5.8.1149 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

Y Jinno, K Sengoku, M Nakao, K Tamate, T Miyamoto, T Matsuzaka, JS Sutcliffe, T Anan, N Takuma, K Nishiwaki, Y Ikeda, T Ishimaru, M Ishikawa, and N Niikawa

Mouse/human sequence divergence in a region with a paternal-specific methylation imprint at the human H19 locus
Hum. Mol. Genet. 1996 5: 1155-1161; doi:10.1093/hmg/5.8.1155 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

J Flint, J Rochette, CF Craddock, C Dode, B Vignes, SW Horsley, L Kearney, VJ Buckle, H Ayyub, and DR Higgs

Chromosomal stabilisation by a subtelomeric rearrangement involving two closely related Alu elements
Hum. Mol. Genet. 1996 5: 1163-1169; doi:10.1093/hmg/5.8.1163 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

A el-Amraoui, I Sahly, S Picaud, J Sahel, M Abitbol, and C Petit

Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells
Hum. Mol. Genet. 1996 5: 1171-1178; doi:10.1093/hmg/5.8.1171 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

V Nigro, G Piluso, A Belsito, L Politano, AA Puca, S Papparella, E Rossi, G Viglietto, MG Esposito, C Abbondanza, N Medici, AM Molinari, G Nigro, and GA Puca

Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein
Hum. Mol. Genet. 1996 5: 1179-1186; doi:10.1093/hmg/5.8.1179 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

T Fagerheim, O Nilssen, P Raeymaekers, V Brox, T Moum, HH Elverland, E Teig, HH Omland, GK Fostad, and L Tranebjaerg

Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family
Hum. Mol. Genet. 1996 5: 1187-1191; doi:10.1093/hmg/5.8.1187 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

SY Xu, M Schwartz, T Rosenberg, and A Gal

A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1
Hum. Mol. Genet. 1996 5: 1193-1197; doi:10.1093/hmg/5.8.1193 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

AN Akarsu, ME Turacli, SG Aktan, M Barsoum-Homsy, L Chevrette, BS Sayli, and M Sarfarazi

A second locus (GLC3B) for primary congenital glaucoma (Buphthalmos) maps to the 1p36 region
Hum. Mol. Genet. 1996 5: 1199-1203; doi:10.1093/hmg/5.8.1199 [Abstract] [FREE Full Text] [PDF] [Request Permissions]  

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