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Journal of Medical Genetics|December 1, 1994
Genetic heterogeneity in hereditary haemorrhagic telangiectasiaM E Porteous, A Curtis, O Williams, et al.Investigative Ophthalmology & Visual Science|December 1, 2001
Expression of Drosophila omb-related T-box genes in the developing human and mouse neural retinaJ C Sowden, J K Holt, M Meins, et al.Journal of Medical Genetics|September 11, 1998
Further refinement of the Usher 2A locus at 1q41D A Bessant, A M Payne, C Plant, et al.The Indian Journal of Medical Research|May 1, 1990
Susceptibility pattern of bacterial isolates to lomefloxacinM K Lalitha, A K Nisha, S S Bhattacharya, et al.Investigative Ophthalmology & Visual Science|August 1, 1997
Genomic organization of the human TIMP-1 gene. Investigation of a causative role in the pathogenesis of X-linked retinitis pigmentosa 2A J Hardcastle, D L Thiselton, M Nayudu, et al.Journal of Medical Genetics|February 1, 1993
Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani familyA Curtis, R J Richardson, J Boohene, et al.American Journal of Physical Anthropology|January 1, 1976
A survey of glucose-6-phosphate-dehydrogenase deficiency in the North Central Province of Sri Lanka (formerly Ceylon)K P Abeyaratne, S Premawansa, L Rajapakse, et al.Annals of the Rheumatic Diseases|February 1, 1992
Contribution of inherited factors to rheumatoid arthritisC M Deighton, J Wentzel, G Cavanagh, et al.American Journal of Physical Anthropology|June 1, 1986
Anthropometry and the biological structure of the Hvar populationP Rudan, D F Roberts, B Janicijevic, et al.Clinical Chemistry|October 1, 1984
Serum copper concentration significantly less in abnormal pregnanciesP K Buamah, M Russell, A Milford-Ward, et al.Pageof 37