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Annals of Human Genetics|January 1, 1996
From Asia to Europe: mitochondrial DNA sequence variability in Bulgarians and TurksF Calafell, P Underhill, A Tolun, et al.Human Mutation|January 4, 2001
Novel mutations in the GALK1 gene in patients with galactokinase deficiencyM Hunter, D Angelicheva, H L Levy, et al.European Journal of Human Genetics : EJHG|August 10, 1999
Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qterD Angelicheva, I Turnev, D Dye, et al.Human Molecular Genetics|July 1, 1995
Double mutant alleles: are they rare?A Savov, D Angelicheva, A Balassopoulou, et al.Neuromuscular Disorders : NMD|October 29, 2000
Hereditary motor and sensory neuropathy-Lom (HMSNL) in a Spanish family: clinical, electrophysiological, pathological and genetic studiesJ Colomer, C Iturriaga, L Kalaydjieva, et al.American Journal of Human Genetics|August 1, 2000
A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23T Rogers, D Chandler, D Angelicheva, et al.Annals of Neurology|July 13, 1999
Hereditary auditory, vestibular, motor, and sensory neuropathy in a Slovenian Roma (Gypsy) kindredD Butinar, J Zidar, L Leonardis, et al.Journal of Medical Genetics|December 6, 2005
A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypesR Gooding, J Colomer, R King, et al.Human Mutation|January 1, 1995
Pancreatic insufficiency and pulmonary disease in German and Slavic cystic fibrosis patients with the R347P mutationR Varon, M Stuhrmann, M Macek, et al.Human Mutation|January 1, 1997
SSCP analysis: a blind sensitivity trialA Jordanova, L Kalaydjieva, A Savov, et al.Pageof 3