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Biochemical and Biophysical Research Communications|January 13, 1998
Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalizationF Toti, V Schindler, J F Riou, et al.Human Genetics|January 1, 1986
Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosomeI Oberlé, G Camerino, C Kloepfer, et al.Clinical Chemistry|August 14, 1998
Teaching the microscopic examination of urine sediment to second year medical students using the Urinalysis-Tutor computer programC Phillips, P J Henderson, L Mandel, et al.Genomics|January 1, 1989
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked markerR Fujita, Y Agid, P Trouillas, et al.Lancet (London, England)|March 23, 1985
Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPsE Bakker, M H Hofker, N Goor, et al.The Journal of Surgical Research|April 20, 2023
Feasibility of Postoperative Day One or Day Two Discharge After Robotic Cardiac SurgeryColin C Yost, Jake L Rosen, Jenna L Mandel, et al.Neurogenetics|March 25, 2000
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1C Ben Hamida, L Cavalier, S Belal, et al.Human Molecular Genetics|January 1, 1996
Deletions in Xq28 in two boys with myotubular myopathy and abnormal genital development define a new contiguous gene syndrome in a 430 kb regionL J Hu, J Laporte, W Kress, et al.Genomics|January 1, 1991
Genetic mapping of new RFLPs at Xq27-q28G K Suthers, I Oberlé, J Nancarrow, et al.Human Mutation|May 2, 2000
MTM1 mutations in X-linked myotubular myopathyJ Laporte, V Biancalana, S M Tanner, et al.Pageof 31