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de la CHAPELLE

Showing results (71-80 of 603) with videos related to

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Annales De Genetique|March 1, 1978
A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three casesB Kaluzewski, A Jokinen, H Hortling, et al.
American Journal of Medical Genetics|January 1, 1980
Dicentric Y chromosome arising via tandem translocationR Herva, I Saarinen, H Savikurki, et al.
Human Genetics|January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndromeA de la Chapelle, R Herva, M Koivisto, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Diastrophic dysplasia gene maps to the distal long arm of chromosome 5J Hästbacka, I Kaitila, P Sistonen, et al.
Biosensors|September 27, 2023
Recent Progresses in Optical Biosensors for Interleukin 6 DetectionMarjan Majdinasab, Marc Lamy de la Chapelle, Jean Louis Marty
Scandinavian Journal of Haematology|October 1, 1980
Higher frequency of 51--clone in bone marrow mitoses after culture than by a direct methodS Knuutila, P Vuopio, G H Borgström, et al.
Nature|January 12, 1984
Genetic evidence of X-Y interchange in a human XX maleA de la Chapelle, P A Tippett, G Wetterstrand, et al.
FEBS Letters|December 10, 1990
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin geneC P Maury, J Kere, R Tolvanen, et al.
Human Genetics|October 1, 1993
Genetic mapping of the erythropoietin receptor geneP Sistonen, A L Träskelin, H Lehväslaiho, et al.
Nucleic Acids Research|May 25, 1991
Refinement of human chromosome 7 map around the pro alpha 2(I)collagen gene by long-range restriction mappingJ Kere, R Tolvanen, H Donis-Keller, et al.
Pageof 61

Showing results (71-80 of 603) with videos related to

Sort By:
Pageof 61
Annales De Genetique|March 1, 1978
A theory explaining the abnormality in 45,X/46,XY mosaicism with non-fluorescent Y chromosome. presentation of three casesB Kaluzewski, A Jokinen, H Hortling, et al.
American Journal of Medical Genetics|January 1, 1980
Dicentric Y chromosome arising via tandem translocationR Herva, I Saarinen, H Savikurki, et al.
Human Genetics|January 1, 1981
A deletion in chromosome 22 can cause DiGeorge syndromeA de la Chapelle, R Herva, M Koivisto, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 1, 1990
Diastrophic dysplasia gene maps to the distal long arm of chromosome 5J Hästbacka, I Kaitila, P Sistonen, et al.
Biosensors|September 27, 2023
Recent Progresses in Optical Biosensors for Interleukin 6 DetectionMarjan Majdinasab, Marc Lamy de la Chapelle, Jean Louis Marty
Scandinavian Journal of Haematology|October 1, 1980
Higher frequency of 51--clone in bone marrow mitoses after culture than by a direct methodS Knuutila, P Vuopio, G H Borgström, et al.
Nature|January 12, 1984
Genetic evidence of X-Y interchange in a human XX maleA de la Chapelle, P A Tippett, G Wetterstrand, et al.
FEBS Letters|December 10, 1990
Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin geneC P Maury, J Kere, R Tolvanen, et al.
Human Genetics|October 1, 1993
Genetic mapping of the erythropoietin receptor geneP Sistonen, A L Träskelin, H Lehväslaiho, et al.
Nucleic Acids Research|May 25, 1991
Refinement of human chromosome 7 map around the pro alpha 2(I)collagen gene by long-range restriction mappingJ Kere, R Tolvanen, H Donis-Keller, et al.
Pageof 61