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D Weil

Showing results (141-150 of 203) with videos related to

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The British Journal of Ophthalmology|October 19, 2004
Treatment of thyroid associated ophthalmopathy with periocular injections of triamcinoloneR Ebner, M H Devoto, D Weil, et al.
Nature Genetics|June 1, 1997
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA geneD Weil, P Küssel, S Blanchard, et al.
The Journal of Biological Chemistry|October 5, 1989
Temperature-dependent expression of a collagen splicing defect in the fibroblasts of a patient with Ehlers-Danlos syndrome type VIID Weil, M D'Alessio, F Ramirez, et al.
The Journal of Biological Chemistry|November 25, 1987
Organization of the human pro-alpha 2(I) collagen geneW de Wet, M Bernard, V Benson-Chanda, et al.
Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.
American Journal of Human Genetics|July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2I Henry, G Uzan, D Weil, et al.
American Journal of Human Genetics|October 23, 1997
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse originsA Adato, D Weil, H Kalinski, et al.
Regenerative Medicine|June 17, 2017
An integrated experimental and economic evaluation of cell therapy affinity purification technologiesBenjamin D Weil, Michael J Jenkins, Siddique Uddin, et al.
Human Genetics|January 1, 1980
Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16V C Nguyen, D Weil, M C Hors-Cayla, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|May 11, 2006
Technical problems and complications of a transanal pull-through for Hirschsprung's diseaseG Podevin, H Lardy, O Azzis, et al.
Pageof 21

Showing results (141-150 of 203) with videos related to

Sort By:
Pageof 21
The British Journal of Ophthalmology|October 19, 2004
Treatment of thyroid associated ophthalmopathy with periocular injections of triamcinoloneR Ebner, M H Devoto, D Weil, et al.
Nature Genetics|June 1, 1997
The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA geneD Weil, P Küssel, S Blanchard, et al.
The Journal of Biological Chemistry|October 5, 1989
Temperature-dependent expression of a collagen splicing defect in the fibroblasts of a patient with Ehlers-Danlos syndrome type VIID Weil, M D'Alessio, F Ramirez, et al.
The Journal of Biological Chemistry|November 25, 1987
Organization of the human pro-alpha 2(I) collagen geneW de Wet, M Bernard, V Benson-Chanda, et al.
Genomics|February 18, 1998
Sequence characterization of a newly identified human alpha-tubulin gene (TUBA2)C Dodé, D Weil, J Levilliers, et al.
American Journal of Human Genetics|July 1, 1984
The genes coding for A alpha-, B beta-, and gamma-chains of fibrinogen map to 4q2I Henry, G Uzan, D Weil, et al.
American Journal of Human Genetics|October 23, 1997
Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, in Usher 1B families from diverse originsA Adato, D Weil, H Kalinski, et al.
Regenerative Medicine|June 17, 2017
An integrated experimental and economic evaluation of cell therapy affinity purification technologiesBenjamin D Weil, Michael J Jenkins, Siddique Uddin, et al.
Human Genetics|January 1, 1980
Assignment of the genes for human lysosomal acid lipases A and B to chromosomes 10 and 16V C Nguyen, D Weil, M C Hors-Cayla, et al.
European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|May 11, 2006
Technical problems and complications of a transanal pull-through for Hirschsprung's diseaseG Podevin, H Lardy, O Azzis, et al.
Pageof 21