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BMC Musculoskeletal Disorders|August 20, 2015
Understanding the information needs of women with rheumatoid arthritis concerning pregnancy, post-natal care and early parenting: A mixed-methods studyIlana N Ackerman, Joanne E Jordan, Sharon Van Doornum, et al.Genes, Chromosomes & Cancer|November 1, 1990
A chromosome jump crosses a translocation breakpoint in the von Recklinghausen neurofibromatosis regionM R Wallace, L B Andersen, J W Fountain, et al.American Journal of Human Genetics|July 1, 1995
Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancerJ P Struewing, L C Brody, M R Erdos, et al.Cancer|August 1, 1994
Familial breast cancer. Approaching the isolation of a susceptibility geneB L Weber, K J Abel, L C Brody, et al.Science (New York, N.Y.)|December 20, 1991
Chloride conductance expressed by delta F508 and other mutant CFTRs in Xenopus oocytesM L Drumm, D J Wilkinson, L S Smit, et al.Biophysical Journal|March 25, 1998
Cystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the poreM K Mansoura, S S Smith, A D Choi, et al.Proceedings of the National Academy of Sciences of the United States of America|November 1, 1990
Identification of mutations in regions corresponding to the two putative nucleotide (ATP)-binding folds of the cystic fibrosis geneB S Kerem, J Zielenski, D Markiewicz, et al.Blood|August 1, 1993
Identification of yeast artificial chromosomes containing the inversion 16 p-arm breakpoint associated with acute myelomonocytic leukemiaP Liu, D F Claxton, P Marlton, et al.Genomics|February 15, 1996
Isolation of tetranucleotide repeat polymorphisms flanking the BRCA1 geneP E Bennett-Baker, S Kiousis, S C Chandrasekharappa, et al.Nature Genetics|February 1, 1993
Mutations in the neurofibromatosis 1 gene in sporadic malignant melanoma cell linesL B Andersen, J W Fountain, D H Gutmann, et al.Pageof 87