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Genomics|September 1, 1993
A radiation hybrid map of the BRCA1 region of chromosome 17q12-q21K J Abel, M Boehnke, M Prahalad, et al.
Genomics|December 1, 1987
Linkage studies with chromosome 17 DNA markers in 45 neurofibromatosis 1 familiesK Stephens, V M Riccardi, M Rising, et al.
American Journal of Human Genetics|January 1, 1989
Genetic analysis of eight loci tightly linked to neurofibromatosis 1K Stephens, P Green, V M Riccardi, et al.
Human Molecular Genetics|August 1, 1993
Molecular basis of defective anion transport in L cells expressing recombinant forms of CFTRY Yang, D C Devor, J F Engelhardt, et al.
Genomics|May 1, 1992
Sequence-tagged sites (STSs) spanning 4p16.3 and the Huntington disease candidate regionJ F Gusella, M R Altherr, A I McClatchey, et al.
Blood|February 1, 1995
Molecular characterization of 16p deletions associated with inversion 16 defines the critical fusion for leukemogenesisP Marlton, D F Claxton, P Liu, et al.
Somatic Cell and Molecular Genetics|September 1, 1995
Localization of the human homolog of the yeast cell division control 27 gene (CDC27) proximal to ITGB3 on human chromosome 17q21.3P P Ho, F J Couch, L C Brody, et al.
The EMBO Journal|March 1, 1992
Transfection of wild-type CFTR into cystic fibrosis lymphocytes restores chloride conductance at G1 of the cell cycleR D Krauss, J K Bubien, M L Drumm, et al.
Molecular and Cellular Biology|November 1, 1992
Phylogenetic footprinting reveals a nuclear protein which binds to silencer sequences in the human gamma and epsilon globin genesD L Gumucio, H Heilstedt-Williamson, T A Gray, et al.
Blood|February 1, 1986
Concordance of a point mutation 5' to the A gamma-globin gene with A gamma beta + hereditary persistence of fetal hemoglobin in GreeksP G Waber, M A Bender, R E Gelinas, et al.
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