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Neurology|January 24, 2002
Genetic identity of Marinesco-Sjögren/myoglobinuria and CCFDN syndromesL Merlini, R Gooding, H Lochmüller, et al.Human Mutation|January 1, 1994
Cystic fibrosis patients from the Black Sea region: the 1677delTA mutationD Angelicheva, K Boteva, A Jordanova, et al.Human Genetics|April 1, 1997
Cystic fibrosis mutations and associated haplotypes in Bulgaria - a comparative population genetic studyD Angelicheva, F Calafell, A Savov, et al.European Journal of Human Genetics : EJHG|April 21, 2001
Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineagesL Kalaydjieva, F Calafell, M A Jobling, et al.Clinical Genetics|June 10, 2008
Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in GypsiesP Sivadorai, S Cherninkova, S Bouwer, et al.American Journal of Human Genetics|June 1, 2000
N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-LomL Kalaydjieva, D Gresham, R Gooding, et al.Annals of Neurology|October 17, 2001
Hereditary motor and sensory neuropathy-russe: new autosomal recessive neuropathy in Balkan GypsiesP K Thomas, L Kalaydjieva, B Youl, et al.American Journal of Human Genetics|October 16, 1999
A founder mutation in the GK1 gene is responsible for galactokinase deficiency in Roma (Gypsies)L Kalaydjieva, A Perez-Lezaun, D Angelicheva, et al.American Journal of Human Genetics|November 13, 2001
Origins and divergence of the Roma (gypsies)D Gresham, B Morar, P A Underhill, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2001
Angiotensin-converting enzyme activity and the ACE Alu polymorphism in autosomal dominant polycystic kidney diseaseT Schiavello, V Burke, N Bogdanova, et al.Pageof 3