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G Tromp

Showing results (61-70 of 80) with videos related to

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Nucleic Acids Research|October 25, 1990
G to A polymorphism in exon 31 of the COL3A1 geneK Zafarullah, C Kleinert, G Tromp, et al.
Journal of Child Neurology|June 8, 2001
A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autismE Asano, H Kuivaniemi, A H Huq, et al.
Current Medical Imaging|February 29, 2020
Colored Video Analysis in Wireless Capsule Endoscopy: A Survey of State-of-the-ArtAmira S Ashour, Nilanjan Dey, Waleed S Mohamed, et al.
Nucleic Acids Research|August 11, 1991
A to G polymorphism in ELN geneG Tromp, A Christiano, N Goldstein, et al.
Clinical Medicine & Research|July 5, 2023
A Cross-Sectional Study of the Physical and Mental Well-Being of Long COVID Patients in ArubaVeronika Duwel, Jaclyn M L de Kort, Caroline M Becker, et al.
Pediatric Research|July 1, 1995
Obesity after successful treatment of acute lymphoblastic leukemia in childhoodJ E Van Dongen-Melman, A C Hokken-Koelega, K Hählen, et al.
Ciba Foundation Symposium|January 1, 1988
Expression of type I procollagen genesD J Prockop, K E Kadler, Y Hojima, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
American Journal of Medical Genetics|September 1, 1989
Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissueD J Prockop, C D Constantinou, K E Dombrowski, et al.
Applied Clinical Informatics|April 16, 2014
A rigorous algorithm to detect and clean inaccurate adult height records within EHR systemsA Muthalagu, J A Pacheco, S Aufox, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|October 25, 1990
G to A polymorphism in exon 31 of the COL3A1 geneK Zafarullah, C Kleinert, G Tromp, et al.
Journal of Child Neurology|June 8, 2001
A study of novel polymorphisms in the upstream region of vasoactive intestinal peptide receptor type 2 gene in autismE Asano, H Kuivaniemi, A H Huq, et al.
Current Medical Imaging|February 29, 2020
Colored Video Analysis in Wireless Capsule Endoscopy: A Survey of State-of-the-ArtAmira S Ashour, Nilanjan Dey, Waleed S Mohamed, et al.
Nucleic Acids Research|August 11, 1991
A to G polymorphism in ELN geneG Tromp, A Christiano, N Goldstein, et al.
Clinical Medicine & Research|July 5, 2023
A Cross-Sectional Study of the Physical and Mental Well-Being of Long COVID Patients in ArubaVeronika Duwel, Jaclyn M L de Kort, Caroline M Becker, et al.
Pediatric Research|July 1, 1995
Obesity after successful treatment of acute lymphoblastic leukemia in childhoodJ E Van Dongen-Melman, A C Hokken-Koelega, K Hählen, et al.
Ciba Foundation Symposium|January 1, 1988
Expression of type I procollagen genesD J Prockop, K E Kadler, Y Hojima, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
American Journal of Medical Genetics|September 1, 1989
Type I procollagen: the gene-protein system that harbors most of the mutations causing osteogenesis imperfecta and probably more common heritable disorders of connective tissueD J Prockop, C D Constantinou, K E Dombrowski, et al.
Applied Clinical Informatics|April 16, 2014
A rigorous algorithm to detect and clean inaccurate adult height records within EHR systemsA Muthalagu, J A Pacheco, S Aufox, et al.
Pageof 8