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J Schmidtke

Showing results (131-140 of 214) with videos related to

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Prenatal Diagnosis|August 12, 2004
Prenatal exclusion without involving the putative fathers of an incestuous father-daughter parenthoodJ Schmidtke, W Kühnau, D Wand, et al.
Human Molecular Genetics|November 1, 1996
Testis-specific protein, Y-encoded (TSPY) expression in testicular tissuesF Schnieders, T Dörk, J Arnemann, et al.
Lancet (London, England)|April 30, 1991
Genetic influences in the formation of nasal polypsJ Bürger, M Macek, M Stuhrmann, et al.
The Journal of Endocrinology|June 1, 1977
Binding of human chorionic gonadotrophin to rat ovary during developmentJ W Siebers, F Peters, M T Zenzes, et al.
Human Mutation|July 29, 1999
Identification of 9 novel FBN1 mutations in German patients with Marfan syndromeA A El-Aleem, M Karck, A Haverich, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Characterization of rearranged Y chromosomes in human testicular tumor cell linesJ Arnemann, G Gradl, J Casper, et al.
Human Mutation|April 29, 1998
A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.
Human Genetics|February 1, 1991
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenitaM Stuhrmann, H Heilbronner, A Reis, et al.
Human Genetics|January 1, 1985
An estimate of unique DNA sequence heterozygosity in the human genomeD N Cooper, B A Smith, H J Cooke, et al.
Dalton Transactions (Cambridge, England : 2003)|December 28, 2020
Lipophilic Re(CO)<sub>3</sub>pyca complexes for Mid-IR imaging applicationsBriana R Schrage, Baylee R Frisinger, Sarah J Schmidtke Sobeck, et al.
Pageof 22

Showing results (131-140 of 214) with videos related to

Sort By:
Pageof 22
Prenatal Diagnosis|August 12, 2004
Prenatal exclusion without involving the putative fathers of an incestuous father-daughter parenthoodJ Schmidtke, W Kühnau, D Wand, et al.
Human Molecular Genetics|November 1, 1996
Testis-specific protein, Y-encoded (TSPY) expression in testicular tissuesF Schnieders, T Dörk, J Arnemann, et al.
Lancet (London, England)|April 30, 1991
Genetic influences in the formation of nasal polypsJ Bürger, M Macek, M Stuhrmann, et al.
The Journal of Endocrinology|June 1, 1977
Binding of human chorionic gonadotrophin to rat ovary during developmentJ W Siebers, F Peters, M T Zenzes, et al.
Human Mutation|July 29, 1999
Identification of 9 novel FBN1 mutations in German patients with Marfan syndromeA A El-Aleem, M Karck, A Haverich, et al.
Cancer Genetics and Cytogenetics|February 1, 1989
Characterization of rearranged Y chromosomes in human testicular tumor cell linesJ Arnemann, G Gradl, J Casper, et al.
Human Mutation|April 29, 1998
A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.
Human Genetics|February 1, 1991
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenitaM Stuhrmann, H Heilbronner, A Reis, et al.
Human Genetics|January 1, 1985
An estimate of unique DNA sequence heterozygosity in the human genomeD N Cooper, B A Smith, H J Cooke, et al.
Dalton Transactions (Cambridge, England : 2003)|December 28, 2020
Lipophilic Re(CO)<sub>3</sub>pyca complexes for Mid-IR imaging applicationsBriana R Schrage, Baylee R Frisinger, Sarah J Schmidtke Sobeck, et al.
Pageof 22