J Schmidtke|W Stille - JoVE Visualize

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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.

Immunitat Und Infektion|July 1, 1992

[Enhanced lymphocyte proliferation in the presence of epidermal cells of HIV-infected patients in vitro]R P Kappus, S Berger, C A Thomas, 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)3pyca complexes for Mid-IR imaging applicationsBriana R Schrage, Baylee R Frisinger, Sarah J Schmidtke Sobeck, et al.

Human Genetics|June 1, 1991

A sterile male with 45,X0 and a Y;22 translocationJ Arnemann, S Schnittger, G K Hinkel, et al.

The Journal of Physical Chemistry. A|June 25, 2009

Structural and spectroscopic studies of the photophysical properties of benzophenone derivativesBrandi M Baughman, Elana Stennett, Rachel E Lipner, et al.

Biology of Reproduction|November 4, 2000

Immortalization of murine male germ cells at a discrete stage of differentiation by a novel directed promoter-based selection strategyS Tascou, K Nayernia, A Samani, et al.

Human Genetics|January 1, 1985

A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequenceJ Schmidtke, J Arnemann, M Schmid, et al.

European Journal of Clinical Pharmacology|May 17, 1978

Effect of aminoglycosides on proximal tubular membranes of the human kidneyA W Mondorf, J Breier, J Hendus, et al.

Journal of Medical Genetics|October 1, 1993

CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553XK Will, J Reiss, M Dean, et al.

Pageof 25

Showing results (171-180 of 246) with videos related to

Sort By:

Pageof 25

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.

Immunitat Und Infektion|July 1, 1992

[Enhanced lymphocyte proliferation in the presence of epidermal cells of HIV-infected patients in vitro]R P Kappus, S Berger, C A Thomas, 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)3pyca complexes for Mid-IR imaging applicationsBriana R Schrage, Baylee R Frisinger, Sarah J Schmidtke Sobeck, et al.

Human Genetics|June 1, 1991

A sterile male with 45,X0 and a Y;22 translocationJ Arnemann, S Schnittger, G K Hinkel, et al.

The Journal of Physical Chemistry. A|June 25, 2009

Structural and spectroscopic studies of the photophysical properties of benzophenone derivativesBrandi M Baughman, Elana Stennett, Rachel E Lipner, et al.

Biology of Reproduction|November 4, 2000

Immortalization of murine male germ cells at a discrete stage of differentiation by a novel directed promoter-based selection strategyS Tascou, K Nayernia, A Samani, et al.

Human Genetics|January 1, 1985

A male with a monocentric Yq isochromosome and presence of a Yp-specific DNA sequenceJ Schmidtke, J Arnemann, M Schmid, et al.

European Journal of Clinical Pharmacology|May 17, 1978

Effect of aminoglycosides on proximal tubular membranes of the human kidneyA W Mondorf, J Breier, J Hendus, et al.

Journal of Medical Genetics|October 1, 1993

CFTR transcripts are undetectable in lymphocytes and respiratory epithelial cells of a CF patient homozygous for the nonsense mutation R553XK Will, J Reiss, M Dean, et al.

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