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G R Stalder

Showing results (11-20 of 25) with videos related to

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Humangenetik|January 1, 1971
A strongly fluorescing abnormal chromosome in a malformed childE M Bühler, H Müller, G R Stalder, et al.
European Journal of Pediatrics|November 3, 1976
Trisomy 8 mosaicism. A case report and a proposed list of the clinical featuresG Kosztolànyi, E M Bühler, P Elmiger, et al.
Nature|December 10, 1971
Variant of the fluorescence pattern in an abnormal human Y chromosomeE M Bühler, H Miller, J Miller, et al.
Humangenetik|January 1, 1972
Cat-eye syndrome, a partial trisomy 22E M Bühler, K Méhes, H Müller, et al.
Schweizerische Medizinische Wochenschrift|August 14, 1971
[A new method of sex determination in leukocytes from dired blood stains]H Müller, E M Bühler, M G Voegelin, et al.
Humangenetik|January 1, 1975
Satellite DNA III and alkaline Geimsa stainingE M Bühler, T Tsuchimoto, L P Jurik, et al.
Helvetica Paediatrica Acta|November 1, 1974
Non-fluorescent Y-chromosomeE M Bühler, U K Bühler, T Tsuchimoto, et al.
Archiv Fur Genetik|January 1, 1974
[A rare structural anomaly of the Y chromosome: Y ring (author's transl)]E M Bühler, T Tsuchimoto, U K Bühler, et al.
Journal of Medical Genetics|December 1, 1972
Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliographyH Müller, E M Bühler, E Signer, et al.
Humangenetik|January 1, 1971
Fluorescence pattern of a dicentric YE M Bühler, R Frey, H Müller, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Humangenetik|January 1, 1971
A strongly fluorescing abnormal chromosome in a malformed childE M Bühler, H Müller, G R Stalder, et al.
European Journal of Pediatrics|November 3, 1976
Trisomy 8 mosaicism. A case report and a proposed list of the clinical featuresG Kosztolànyi, E M Bühler, P Elmiger, et al.
Nature|December 10, 1971
Variant of the fluorescence pattern in an abnormal human Y chromosomeE M Bühler, H Miller, J Miller, et al.
Humangenetik|January 1, 1972
Cat-eye syndrome, a partial trisomy 22E M Bühler, K Méhes, H Müller, et al.
Schweizerische Medizinische Wochenschrift|August 14, 1971
[A new method of sex determination in leukocytes from dired blood stains]H Müller, E M Bühler, M G Voegelin, et al.
Humangenetik|January 1, 1975
Satellite DNA III and alkaline Geimsa stainingE M Bühler, T Tsuchimoto, L P Jurik, et al.
Helvetica Paediatrica Acta|November 1, 1974
Non-fluorescent Y-chromosomeE M Bühler, U K Bühler, T Tsuchimoto, et al.
Archiv Fur Genetik|January 1, 1974
[A rare structural anomaly of the Y chromosome: Y ring (author's transl)]E M Bühler, T Tsuchimoto, U K Bühler, et al.
Journal of Medical Genetics|December 1, 1972
Trisomy-18 syndrome caused by translocation or isochromosome formation. A case report with bibliographyH Müller, E M Bühler, E Signer, et al.
Humangenetik|January 1, 1971
Fluorescence pattern of a dicentric YE M Bühler, R Frey, H Müller, et al.
Pageof 3