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Journal of Cellular Physiology|October 1, 1982
Dissociation of hemoglobin accumulation and commitment during murine erythroleukemia cell differentiation by treatment with imidazoleJ F Gusella, A S Tsiftsoglou, V Volloch, et al.
Human Molecular Genetics|October 1, 1992
The genomic structure of the human skeletal muscle sodium channel geneA I McClatchey, C S Lin, J Wang, et al.
American Journal of Human Genetics|December 1, 1993
An index marker map of chromosome 9 provides strong evidence for positive interferenceD J Kwiatkowski, C Dib, S A Slaugenhaupt, et al.
DNA and Cell Biology|December 1, 1992
Complete human NF1 cDNA sequence: two alternatively spliced mRNAs and absence of expression in a neuroblastoma lineA Bernards, V H Haase, A E Murthy, et al.
Human Genetics|June 1, 1987
Localization of the ornithine aminotransferase gene and related sequences on two human chromosomesV Ramesh, R Eddy, G A Bruns, et al.
Genetic Epidemiology|January 1, 1987
Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysisP L Kramer, L Ozelius, J F Gusella, et al.
American Journal of Medical Genetics|November 20, 1995
Prenatal diagnosis of familial dysautonomia by analysis of linked CA-repeat polymorphisms on chromosome 9q31-q33C M Eng, S A Slaugenhaupt, A Blumenfeld, et al.
American Journal of Human Genetics|July 1, 1993
The normal Huntington disease (HD) allele, or a closely linked gene, influences age at onset of HDL A Farrer, L A Cupples, P Wiater, et al.
Neurogenetics|February 7, 2001
Allelic expression of the NF2 gene in neurofibromatosis 2 and schwannomatosisL B Jacoby, M MacCollin, D M Parry, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Different gene loci for hyperkalemic and hypokalemic periodic paralysisB Fontaine, J Trofatter, G A Rouleau, et al.
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