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Clinical Genetics
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May 23, 2006
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12
S Malik, A A Abbasi, M Ansar, et al.
Molecular and Cellular Biology
|
May 29, 2008
Sox12 deletion in the mouse reveals nonreciprocal redundancy with the related Sox4 and Sox11 transcription factors
Melanie Hoser, Michaela R Potzner, Julia M C Koch, et al.
American Journal of Medical Genetics
|
October 21, 1999
Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)
K Stegmann, A Ziegler, E T Ngo, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 1, 1996
Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome
L Károlyi, A Ziegler, M Pollak, et al.
Neurology
|
August 1, 1994
Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts
K Ricker, M C Koch, F Lehmann-Horn, et al.
Der Pathologe
|
October 21, 2015
[S3 guidelines on diagnostics and treatment of cervical cancer: Demands on pathology]
L-C Horn, M W Beckmann, M Follmann, et al.
Vox Sanguinis
|
May 22, 1998
Routine screening of blood donations for HCV RNA
F M Araújo, M C Koch, I Henriques, et al.
Transfusion
|
June 16, 2001
The first case of HCV seroconversion in Portugal after the introduction of HCV NAT screening
F M Araújo, I Henriques, F Monteiro, et al.
Journal of Medical Genetics
|
November 1, 1993
Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker)
M C Koch, K Ricker, M Otto, et al.
Der Nervenarzt
|
June 1, 1995
[Myotonic dystrophy: magnetic resonance tomography and clinico-genetic correlations]
M S Damian, M C Koch, G Bachmann, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 59) with videos related to
Sort By:
Page
of 6
Clinical Genetics
|
May 23, 2006
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12
S Malik, A A Abbasi, M Ansar, et al.
Molecular and Cellular Biology
|
May 29, 2008
Sox12 deletion in the mouse reveals nonreciprocal redundancy with the related Sox4 and Sox11 transcription factors
Melanie Hoser, Michaela R Potzner, Julia M C Koch, et al.
American Journal of Medical Genetics
|
October 21, 1999
Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD)
K Stegmann, A Ziegler, E T Ngo, et al.
Pediatric Nephrology (Berlin, Germany)
|
October 1, 1996
Gitelman's syndrome is genetically distinct from other forms of Bartter's syndrome
L Károlyi, A Ziegler, M Pollak, et al.
Neurology
|
August 1, 1994
Proximal myotonic myopathy: a new dominant disorder with myotonia, muscle weakness, and cataracts
K Ricker, M C Koch, F Lehmann-Horn, et al.
Der Pathologe
|
October 21, 2015
[S3 guidelines on diagnostics and treatment of cervical cancer: Demands on pathology]
L-C Horn, M W Beckmann, M Follmann, et al.
Vox Sanguinis
|
May 22, 1998
Routine screening of blood donations for HCV RNA
F M Araújo, M C Koch, I Henriques, et al.
Transfusion
|
June 16, 2001
The first case of HCV seroconversion in Portugal after the introduction of HCV NAT screening
F M Araújo, I Henriques, F Monteiro, et al.
Journal of Medical Genetics
|
November 1, 1993
Evidence for genetic homogeneity in autosomal recessive generalised myotonia (Becker)
M C Koch, K Ricker, M Otto, et al.
Der Nervenarzt
|
June 1, 1995
[Myotonic dystrophy: magnetic resonance tomography and clinico-genetic correlations]
M S Damian, M C Koch, G Bachmann, et al.
Page
of 6