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K Zerres

Showing results (151-160 of 174) with videos related to

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Genetic Testing|August 28, 1999
Mutations in the SLC3A1 gene in cystinuric patients: frequencies and identification of a novel mutationA Albers, S Lahme, C Wagner, et al.
Genes & Development|August 1, 1997
Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2betaM Moser, A Pscherer, C Roth, et al.
American Journal of Medical Genetics|December 23, 1999
Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6pC Hallermann, G Mücher, N Kohlschmidt, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 21, 2003
The interleukin-6 promoter polymorphism is associated with elevated leukocyte, lymphocyte, and monocyte counts and reduced physical fitness in young healthy smokersJ R Ortlepp, J Metrikat, K Vesper, et al.
American Journal of Human Genetics|December 1, 1994
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophyC J DiDonato, K Morgan, J D Carpten, et al.
Lancet (London, England)|July 5, 1986
Prenatal diagnosis of autosomal dominant polycystic kidney disease with a DNA probeS T Reeders, K Zerres, A Gal, et al.
Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.
Annals of Neurology|October 23, 1997
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy regionR Korinthenberg, M Sauer, U P Ketelsen, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney diseaseY Hofmann, J Becker, F Wright, et al.
Genomics|March 21, 1998
Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2 beta, and GSTA1 at 6p21.1-p12G Mücher, J Becker, M Knapp, et al.
Pageof 18

Showing results (151-160 of 174) with videos related to

Sort By:
Pageof 18
Genetic Testing|August 28, 1999
Mutations in the SLC3A1 gene in cystinuric patients: frequencies and identification of a novel mutationA Albers, S Lahme, C Wagner, et al.
Genes & Development|August 1, 1997
Enhanced apoptotic cell death of renal epithelial cells in mice lacking transcription factor AP-2betaM Moser, A Pscherer, C Roth, et al.
American Journal of Medical Genetics|December 23, 1999
Syndrome of autosomal recessive polycystic kidneys with skeletal and facial anomalies is not linked to the ARPKD gene locus on chromosome 6pC Hallermann, G Mücher, N Kohlschmidt, et al.
Journal of Molecular Medicine (Berlin, Germany)|August 21, 2003
The interleukin-6 promoter polymorphism is associated with elevated leukocyte, lymphocyte, and monocyte counts and reduced physical fitness in young healthy smokersJ R Ortlepp, J Metrikat, K Vesper, et al.
American Journal of Human Genetics|December 1, 1994
Association between Ag1-CA alleles and severity of autosomal recessive proximal spinal muscular atrophyC J DiDonato, K Morgan, J D Carpten, et al.
Lancet (London, England)|July 5, 1986
Prenatal diagnosis of autosomal dominant polycystic kidney disease with a DNA probeS T Reeders, K Zerres, A Gal, et al.
Genomics|February 1, 1992
Linkage analysis of spinal muscular atrophyR J Daniels, N H Thomas, R N MacKinnon, et al.
Annals of Neurology|October 23, 1997
Congenital axonal neuropathy caused by deletions in the spinal muscular atrophy regionR Korinthenberg, M Sauer, U P Ketelsen, et al.
European Journal of Human Genetics : EJHG|April 26, 2000
Genomic structure of the gene for the human P1 protein (MCM3) and its exclusion as a candidate for autosomal recessive polycystic kidney diseaseY Hofmann, J Becker, F Wright, et al.
Genomics|March 21, 1998
Fine mapping of the autosomal recessive polycystic kidney disease locus (PKHD1) and the genes MUT, RDS, CSNK2 beta, and GSTA1 at 6p21.1-p12G Mücher, J Becker, M Knapp, et al.
Pageof 18