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European Journal of Paediatric Dentistry
|
June 20, 2022
Ectodermal dysplasia: important role of complex dental care in its interdisciplinary management
L Kratochvilova, T Dostalova, M Schwarz, et al.
Human Mutation
|
January 11, 1992
Identification of a novel nonsense mutation (L88X) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene in a native Korean cystic fibrosis chromosome
M Macek, A Hamosh, S Kiesewetter, et al.
Ceskoslovenska Pediatrie
|
November 1, 1987
[The fragile X chromosome syndrome]
E Seemanová, A Schmidt, I Subrt, et al.
Ceska Gynekologie
|
October 20, 2000
[Fetal nucleated erythrocytes in the peripheral circulation of pregnant women as a noninvasive method of fetal sex determination]
I Hromadíková, S Karamanov, M Mrstinová, et al.
Ceskoslovenska Pediatrie
|
March 1, 1988
[Changes in gamma-glutamyltransferase activity of the amniotic fluid in fetuses with severe disorders of prenatal development]
M Macek, H Tomásová, J Hronková, et al.
Sbornik Lekarsky
|
January 1, 1997
The invasive prenatal diagnosis in perinatal centre
Z Hájek, T Koleska, P Drbohlav, et al.
Casopis Lekaru Ceskych
|
December 24, 2003
[Chromosome Y microdeletions in Czech men with severe reproductive disorders]
M Machatková, A Krebsová, I Smetanová, et al.
Casopis Lekaru Ceskych
|
May 29, 1987
[Initial experience with the diagnosis of hemophilia A using molecular genetics]
Z Sedlácek, M Macek, S Malcolm, et al.
Casopis Lekaru Ceskych
|
June 7, 2012
[Prenatal diagnosis of lysosomal enzymopathies in the Czech Republic]
H Poupetová, J Ledvinová, D Chudoba, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1975
Cytochemical and cytogenetic findings in five human leukocyte long-term cultures (LAHL) of different origin
V Pössnerová, M Macek, F Hermanský, et al.
Page
of 22
Search research articles
Search
Showing results (131-140 of 217) with videos related to
Sort By:
Page
of 22
European Journal of Paediatric Dentistry
|
June 20, 2022
Ectodermal dysplasia: important role of complex dental care in its interdisciplinary management
L Kratochvilova, T Dostalova, M Schwarz, et al.
Human Mutation
|
January 11, 1992
Identification of a novel nonsense mutation (L88X) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene in a native Korean cystic fibrosis chromosome
M Macek, A Hamosh, S Kiesewetter, et al.
Ceskoslovenska Pediatrie
|
November 1, 1987
[The fragile X chromosome syndrome]
E Seemanová, A Schmidt, I Subrt, et al.
Ceska Gynekologie
|
October 20, 2000
[Fetal nucleated erythrocytes in the peripheral circulation of pregnant women as a noninvasive method of fetal sex determination]
I Hromadíková, S Karamanov, M Mrstinová, et al.
Ceskoslovenska Pediatrie
|
March 1, 1988
[Changes in gamma-glutamyltransferase activity of the amniotic fluid in fetuses with severe disorders of prenatal development]
M Macek, H Tomásová, J Hronková, et al.
Sbornik Lekarsky
|
January 1, 1997
The invasive prenatal diagnosis in perinatal centre
Z Hájek, T Koleska, P Drbohlav, et al.
Casopis Lekaru Ceskych
|
December 24, 2003
[Chromosome Y microdeletions in Czech men with severe reproductive disorders]
M Machatková, A Krebsová, I Smetanová, et al.
Casopis Lekaru Ceskych
|
May 29, 1987
[Initial experience with the diagnosis of hemophilia A using molecular genetics]
Z Sedlácek, M Macek, S Malcolm, et al.
Casopis Lekaru Ceskych
|
June 7, 2012
[Prenatal diagnosis of lysosomal enzymopathies in the Czech Republic]
H Poupetová, J Ledvinová, D Chudoba, et al.
Advances in Experimental Medicine and Biology
|
January 1, 1975
Cytochemical and cytogenetic findings in five human leukocyte long-term cultures (LAHL) of different origin
V Pössnerová, M Macek, F Hermanský, et al.
Page
of 22