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Genetic Epidemiology|January 1, 1988
Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genesJ L Haines, L Ozelius, P St George-Hyslop, et al.Cancer Genetics and Cytogenetics|October 1, 1995
Neurofibromatosis 2 gene in human colorectal cancerA K Rustgi, L Xu, D Pinney, et al.Genomics|May 20, 1995
Mapping of the gene for the Mel1a-melatonin receptor to human chromosome 4 (MTNR1A) and mouse chromosome 8 (Mtnr1a)S A Slaugenhaupt, A L Roca, C B Liebert, et al.Genome Research|October 1, 1995
An expression-independent catalog of genes from human chromosome 22J A Trofatter, K R Long, J R Murrell, et al.American Journal of Medical Genetics|November 1, 1992
Molecular detection of a 4p deletion using PCR-based polymorphisms: a technique for the rapid detection of the Wolf-Hirschhorn syndromeM R Altherr, J F Gusella, J J Wasmuth, et al.Gene|November 1, 1979
The organization of a nuclear DNA sequence from a higher plant: molecular cloning and characterization of soybean ribosomal DNAA Varsanyi-Breiner, J F Gusella, C Keys, et al.Nature|February 11, 1988
Protease inhibitor domain encoded by an amyloid protein precursor mRNA associated with Alzheimer's diseaseR E Tanzi, A I McClatchey, E D Lamperti, et al.American Journal of Human Genetics|April 1, 1988
Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomesM Münke, B Foellmer, P C Watkins, et al.American Journal of Human Genetics|November 1, 1990
Equal parental origin of chromosome 22 losses in human sporadic meningioma: no evidence for genomic imprintingB Fontaine, G A Rouleau, B Seizinger, et al.Genomics|December 1, 1991
A gene encoding a fibroblast growth factor receptor isolated from the Huntington disease gene region of human chromosome 4L M Thompson, S Plummer, M Schalling, et al.Pageof 29