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Clinical Genetics|February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosisO M'hamdi, C Redin, C Stoetzel, et al.Journal of Cardiac Surgery|November 24, 2022
Routine endoscopic robotic cardiac tumor resection using an 8-mm working port and percutaneous cannulationJake L Rosen, Colin C Yost, Daniella H Wong, et al.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.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.Molecular Psychiatry|March 24, 1999
Polyglutamine-containing proteins in schizophreniaR Joober, C Benkelfat, M Jannatipour, et al.Pageof 32