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Journal of Medical Screening
|
October 27, 2001
Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience
C Zekanowski, M Nowacka, B Radomyska, et al.
Neurobiology of Aging
|
August 31, 2016
Parkinson's disease-related gene variants influence pre-mRNA splicing processes
K Gaweda-Walerych, F Mohagheghi, C Zekanowski, et al.
Genetic Testing
|
September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemia
C Zekanowski, M Nowacka, M Gizewska, et al.
Klinika Oczna
|
July 6, 2000
[The attempt to identify mutations in TIGR gene in Polish patients with primary open angle glaucoma]
J Szaflik, A M Ambroziak, J Bal, et al.
Molecular and Cellular Probes
|
August 1, 1994
Frequencies of the most common mutations responsible for phenylketonuria in Poland
C Zekanowski, M Nowacka, M Zgulska, et al.
Dermatology (Basel, Switzerland)
|
September 6, 2000
Parakeratosis variegata: a possible role of environmental hazards?
T T Rogoziński, C Zekanowski, L Kaldan, et al.
Journal of Intellectual Disability Research : JIDR
|
January 25, 2003
Different presentations of late-detected phenylketonuria in two brothers with the same R408W/R111X genotype in the PAH gene
M Gizewska, B Cabalska, L Cyrytowski, et al.
Medycyna Wieku Rozwojowego
|
July 27, 2000
[Mutations causing hereditary hyperphenylalaninemia]
C Zekanowski, M Nowacka, B Cabalska, et al.
Scandinavian Journal of Medicine & Science in Sports
|
May 4, 2016
Genetic variants associated with physical and mental characteristics of the elite athletes in the Polish population
B Peplonska, J G Adamczyk, M Siewierski, et al.
Journal of Inherited Metabolic Disease
|
March 27, 2009
Maternal tetrahydrobiopterin deficiency: the course of two pregnancies and follow-up of two children in a mother with 6-pyruvoyl-tetrahydropterin synthase deficiency
M Giżewska, G Hnatyszyn, L Sagan, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Journal of Medical Screening
|
October 27, 2001
Should newborn mutation scanning for hyperphenylalaninaemia and galactosaemia be implemented? A Polish experience
C Zekanowski, M Nowacka, B Radomyska, et al.
Neurobiology of Aging
|
August 31, 2016
Parkinson's disease-related gene variants influence pre-mRNA splicing processes
K Gaweda-Walerych, F Mohagheghi, C Zekanowski, et al.
Genetic Testing
|
September 25, 1999
Mutations in exon 3 of the PAH gene causing mild hyperphenylalaninemia
C Zekanowski, M Nowacka, M Gizewska, et al.
Klinika Oczna
|
July 6, 2000
[The attempt to identify mutations in TIGR gene in Polish patients with primary open angle glaucoma]
J Szaflik, A M Ambroziak, J Bal, et al.
Molecular and Cellular Probes
|
August 1, 1994
Frequencies of the most common mutations responsible for phenylketonuria in Poland
C Zekanowski, M Nowacka, M Zgulska, et al.
Dermatology (Basel, Switzerland)
|
September 6, 2000
Parakeratosis variegata: a possible role of environmental hazards?
T T Rogoziński, C Zekanowski, L Kaldan, et al.
Journal of Intellectual Disability Research : JIDR
|
January 25, 2003
Different presentations of late-detected phenylketonuria in two brothers with the same R408W/R111X genotype in the PAH gene
M Gizewska, B Cabalska, L Cyrytowski, et al.
Medycyna Wieku Rozwojowego
|
July 27, 2000
[Mutations causing hereditary hyperphenylalaninemia]
C Zekanowski, M Nowacka, B Cabalska, et al.
Scandinavian Journal of Medicine & Science in Sports
|
May 4, 2016
Genetic variants associated with physical and mental characteristics of the elite athletes in the Polish population
B Peplonska, J G Adamczyk, M Siewierski, et al.
Journal of Inherited Metabolic Disease
|
March 27, 2009
Maternal tetrahydrobiopterin deficiency: the course of two pregnancies and follow-up of two children in a mother with 6-pyruvoyl-tetrahydropterin synthase deficiency
M Giżewska, G Hnatyszyn, L Sagan, et al.
Page
of 3