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J G Zimowski

Showing results (1-10 of 14) 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.
Biochimica Et Biophysica Acta|October 11, 1979
Specificity of sterol-glucosylating enzymes from Sinapis alba and Physarum polycephalumZ A Wojciechowski, J Zimowski, J G Zimowski, et al.
Clinical Genetics|January 11, 2016
First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplificationJ G Zimowski, D Massalska, M Pawelec, 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.
Human Mutation|November 26, 1999
Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favismE Jablonska-Skwiecinska, I Lewandowska, D Plochocka, 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.
Clinical Genetics|May 21, 2016
Prenatal diagnosis of congenital myopathies and muscular dystrophiesD Massalska, J G Zimowski, J Bijok, et al.
Pageof 2

Showing results (1-10 of 14) 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.
Biochimica Et Biophysica Acta|October 11, 1979
Specificity of sterol-glucosylating enzymes from Sinapis alba and Physarum polycephalumZ A Wojciechowski, J Zimowski, J G Zimowski, et al.
Clinical Genetics|January 11, 2016
First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplificationJ G Zimowski, D Massalska, M Pawelec, 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.
Human Mutation|November 26, 1999
Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favismE Jablonska-Skwiecinska, I Lewandowska, D Plochocka, 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.
Clinical Genetics|May 21, 2016
Prenatal diagnosis of congenital myopathies and muscular dystrophiesD Massalska, J G Zimowski, J Bijok, et al.
Pageof 2