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K Zerres

Showing results (31-40 of 174) with videos related to

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Geburtshilfe Und Frauenheilkunde|October 1, 1988
[Trisomy 22--prenatal findings in various developmental stages]K Zerres, M Niesen, G Schwanitz, et al.
Klinische Padiatrie|May 1, 1996
[X-chromosomal recessive hydrocephalus internus: a separate disease picture? 2 further case reports and review of the literature]F Haverkamp, A Krämer, H Fahnenstich, et al.
Prenatal Diagnosis|March 1, 1986
Mosaicism of isochromosome 18p. Cytogenetic and morphological findings in a male fetus at 21 weeksH Göcke, I Muradow, K Zerres, et al.
Prenatal Diagnosis|March 1, 1988
Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosisK Zerres, M Hansmann, R Mallmann, et al.
Human Genetics|January 1, 1985
Prenatal diagnosis of genetically determined early manifestation of autosomal dominant polycystic kidney disease?K Zerres, M Hansmann, G Knöpfle, et al.
Der Nervenarzt|September 12, 2003
[Psychiatric and ethical aspects of genetic diagnosis exemplified by Huntington chorea]U Meincke, Ch Kosinski, K Zerres, et al.
Human Heredity|September 1, 1996
A HhaI polymorphism in the human MEP1A gene encoding the alpha subunit of the metalloendopeptidase meprinG Dewald, H U Schildhaus, G Mücher, et al.
Neurology|October 1, 1993
Pregnancy and delivery in Charcot-Marie-Tooth disease type 1S Rudnik-Schöneborn, D Röhrig, G Nicholson, et al.
Klinische Padiatrie|May 1, 1996
[Indirect genotype analysis in 2 families with early manifestation of autosome dominant polycystic nephropathy]V Schuster, S Uhlhaas, A E Horwitz, et al.
Journal of Neurology|January 1, 1992
Pregnancy and spinal muscular atrophyS Rudnik-Schöneborn, K Zerres, J Ignatius, et al.
Pageof 18

Showing results (31-40 of 174) with videos related to

Sort By:
Pageof 18
Geburtshilfe Und Frauenheilkunde|October 1, 1988
[Trisomy 22--prenatal findings in various developmental stages]K Zerres, M Niesen, G Schwanitz, et al.
Klinische Padiatrie|May 1, 1996
[X-chromosomal recessive hydrocephalus internus: a separate disease picture? 2 further case reports and review of the literature]F Haverkamp, A Krämer, H Fahnenstich, et al.
Prenatal Diagnosis|March 1, 1986
Mosaicism of isochromosome 18p. Cytogenetic and morphological findings in a male fetus at 21 weeksH Göcke, I Muradow, K Zerres, et al.
Prenatal Diagnosis|March 1, 1988
Autosomal recessive polycystic kidney disease. Problems of prenatal diagnosisK Zerres, M Hansmann, R Mallmann, et al.
Human Genetics|January 1, 1985
Prenatal diagnosis of genetically determined early manifestation of autosomal dominant polycystic kidney disease?K Zerres, M Hansmann, G Knöpfle, et al.
Der Nervenarzt|September 12, 2003
[Psychiatric and ethical aspects of genetic diagnosis exemplified by Huntington chorea]U Meincke, Ch Kosinski, K Zerres, et al.
Human Heredity|September 1, 1996
A HhaI polymorphism in the human MEP1A gene encoding the alpha subunit of the metalloendopeptidase meprinG Dewald, H U Schildhaus, G Mücher, et al.
Neurology|October 1, 1993
Pregnancy and delivery in Charcot-Marie-Tooth disease type 1S Rudnik-Schöneborn, D Röhrig, G Nicholson, et al.
Klinische Padiatrie|May 1, 1996
[Indirect genotype analysis in 2 families with early manifestation of autosome dominant polycystic nephropathy]V Schuster, S Uhlhaas, A E Horwitz, et al.
Journal of Neurology|January 1, 1992
Pregnancy and spinal muscular atrophyS Rudnik-Schöneborn, K Zerres, J Ignatius, et al.
Pageof 18