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Journal of Medical Genetics|July 5, 2005
Molecular genetics of autosomal dominant retinitis pigmentosa (ADRP): a comprehensive study of 43 Italian familiesC Ziviello, F Simonelli, F Testa, et al.Journal of Medical Genetics|July 5, 2005
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)P J Ferguson, S Chen, M K Tayeh, et al.Journal of Medical Genetics|July 5, 2005
Cloned fusion product from a rare t(15;19)(q13.2;p13.1) inhibit S phase in vitroN Haruki, K S Kawaguchi, S Eichenberger, et al.Journal of Medical Genetics|July 5, 2005
Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studiesA C Antoniou, P D P Pharoah, S Narod, et al.Journal of Medical Genetics|June 28, 2005
Breakpoints around the HOXD cluster result in various limb malformationsB Dlugaszewska, A Silahtaroglu, C Menzel, et al.Journal of Medical Genetics|June 28, 2005
Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parentsC Rosenberg, J Knijnenburg, E Bakker, et al.Journal of Medical Genetics|May 24, 2005
Survivin-directed RNA interference cocktail is a potent suppressor of tumour growth in vivoH Caldas, M P Holloway, B M Hall, et al.Journal of Medical Genetics|May 24, 2005
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasiaK A Kaiser-Rogers, D E McFadden, C A Livasy, et al.Journal of Medical Genetics|June 7, 2005
Genetics of familial intrahepatic cholestasis syndromesS W C van Mil, R H J Houwen, L W J KlompJournal of Medical Genetics|June 7, 2005
Murine candidate bleomycin induced pulmonary fibrosis susceptibility genes identified by gene expression and sequence analysis of linkage regionsC K Haston, T G Tomko, N Godin, et al.Pageof 649