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M Bisko

Showing results (1-10 of 13) with videos related to

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Medycyna Wieku Rozwojowego|July 27, 2000
[Germline mosaicism in a family with Duchenne muscular dystrophy]J G Zimowski, M Bisko, J Zaremba
European Journal of Human Genetics : EJHG|January 1, 1996
Arylsulfatase A pseudodeficiency--incidence in PolandB Czartoryska, J G Zimowski, M Bisko, et al.
Neurologia I Neurochirurgia Polska|May 3, 2000
[Carrier's detection in families affected by Duchenne/Becker muscular dystrophy in which DNA from affected individuals is not available]M Bisko, J G Zimowski, E Fidziańska, et al.
Neurologia I Neurochirurgia Polska|January 1, 1994
[Separation of dystrophinopathies from the group previously classified as limb-girdle muscular dystrophies]M Kozłowska, K Bushby, M Bisko, et al.
Neurologia I Neurochirurgia Polska|May 3, 2000
[Detecting carriers of a deletion in the dystrophin gene in families with a single case of Duchenne/Becker muscular dystrophy]M Bisko, J G Zimowski, D Hoffman-Zacharska, et al.
European Journal of Human Genetics : EJHG|January 1, 1997
Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Poland--a study on the 563 and 1311 mutations of the G6PD geneE Jabłońska-Skwiecińska, J G Zimowski, J Kłopocka, et al.
Acta Biochimica Polonica|January 1, 1994
Evolutionary conservation of the transcribed spacer sequences of the rDNA repeat unit in three species of the genus AspergillusP Borsuk, M Gniadkowski, R Kucharski, et al.
European Neurology|August 31, 2000
Prevalence of arylsulfatase A pseudodeficiency allele in metachromatic leukodystrophy patients from PolandA Lugowska, B Czartoryska, A Tylki-Szymańska, et al.
Neurologia I Neurochirurgia Polska|March 1, 1996
[Detection of dystrophin gene mutation carrier state]M Bisko, J G Zimowski, E Fidziańska, et al.
Dementia and Geriatric Cognitive Disorders|March 8, 2000
Apolipoprotein E genotype and lipid and lipoprotein levels in dementiaH Wehr, T Parnowski, S Puzyński, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Medycyna Wieku Rozwojowego|July 27, 2000
[Germline mosaicism in a family with Duchenne muscular dystrophy]J G Zimowski, M Bisko, J Zaremba
European Journal of Human Genetics : EJHG|January 1, 1996
Arylsulfatase A pseudodeficiency--incidence in PolandB Czartoryska, J G Zimowski, M Bisko, et al.
Neurologia I Neurochirurgia Polska|May 3, 2000
[Carrier's detection in families affected by Duchenne/Becker muscular dystrophy in which DNA from affected individuals is not available]M Bisko, J G Zimowski, E Fidziańska, et al.
Neurologia I Neurochirurgia Polska|January 1, 1994
[Separation of dystrophinopathies from the group previously classified as limb-girdle muscular dystrophies]M Kozłowska, K Bushby, M Bisko, et al.
Neurologia I Neurochirurgia Polska|May 3, 2000
[Detecting carriers of a deletion in the dystrophin gene in families with a single case of Duchenne/Becker muscular dystrophy]M Bisko, J G Zimowski, D Hoffman-Zacharska, et al.
European Journal of Human Genetics : EJHG|January 1, 1997
Erythrocyte glucose-6-phosphate dehydrogenase deficiency in Poland--a study on the 563 and 1311 mutations of the G6PD geneE Jabłońska-Skwiecińska, J G Zimowski, J Kłopocka, et al.
Acta Biochimica Polonica|January 1, 1994
Evolutionary conservation of the transcribed spacer sequences of the rDNA repeat unit in three species of the genus AspergillusP Borsuk, M Gniadkowski, R Kucharski, et al.
European Neurology|August 31, 2000
Prevalence of arylsulfatase A pseudodeficiency allele in metachromatic leukodystrophy patients from PolandA Lugowska, B Czartoryska, A Tylki-Szymańska, et al.
Neurologia I Neurochirurgia Polska|March 1, 1996
[Detection of dystrophin gene mutation carrier state]M Bisko, J G Zimowski, E Fidziańska, et al.
Dementia and Geriatric Cognitive Disorders|March 8, 2000
Apolipoprotein E genotype and lipid and lipoprotein levels in dementiaH Wehr, T Parnowski, S Puzyński, et al.
Pageof 2