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JID Innovations : Skin Science From Molecules to Population Health|December 19, 2024
Identifying Subsets of Cancer Patients with an Increased Risk of Developing Cutaneous Melanoma: A Surveillance, Epidemiology, and End Results-Based AnalysisThomas Z Rohan, Jenna L Mandel, Henry Y Yang, et al.
American Journal of Human Genetics|December 1, 1992
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locusS Belal, K Panayides, G Sirugo, et al.
Human Genetics|March 1, 1988
Multilocus analysis of the fragile X syndromeW T Brown, A Gross, C Chan, et al.
Journal of Medical Genetics|December 1, 1994
X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684)N Dahl, F Samson, N S Thomas, et al.
Journal of Inherited Metabolic Disease|January 1, 1996
ALDP expression in fibroblasts of patients with X-linked adrenoleukodystrophyS Kemp, P A Mooyer, P A Bolhuis, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblastsN Cartier, J Lopez, P Moullier, et al.
Human Genetics|January 1, 1985
Segregation analysis of a marker localised Xp21.2-Xp21.3 in Duchenne and Becker muscular dystrophy familiesH Dorkins, C Junien, J L Mandel, et al.
The Journal of Clinical Investigation|May 1, 1984
Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX geneL Grunebaum, J P Cazenave, G Camerino, et al.
Neurology|November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian familiesM Ben Hamida, S Belal, G Sirugo, et al.
American Journal of Medical Genetics|February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA intervalI Oberlé, A Vincent, N Abbadi, et al.
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