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Showing results (11-20 of 16) with videos related to

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Annals of Burns and Fire Disasters|January 1, 2025
Burn hypertrophy scarring assessment based on patient and observer scar assessment scale (POSAS)M H Oley, M C Oley, F L F G Langi, et al.
American Journal of Medical Genetics|April 15, 1994
Nevoid basal cell carcinoma syndrome: review of 118 affected individualsS Shanley, J Ratcliffe, A Hockey, et al.
American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 17, 2007
Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutationsY W A Jeske, I N McGown, D M Cowley, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 geneM R Davis, E Haan, H Jungbluth, et al.
American Journal of Human Genetics|June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeD Beysen, J Raes, B P Leroy, et al.
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Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Annals of Burns and Fire Disasters|January 1, 2025
Burn hypertrophy scarring assessment based on patient and observer scar assessment scale (POSAS)M H Oley, M C Oley, F L F G Langi, et al.
American Journal of Medical Genetics|April 15, 1994
Nevoid basal cell carcinoma syndrome: review of 118 affected individualsS Shanley, J Ratcliffe, A Hockey, et al.
American Journal of Human Genetics|September 1, 1993
Further localization of the gene for nevoid basal cell carcinoma syndrome (NBCCS) in 15 Australasian families: linkage and loss of heterozygosityG Chenevix-Trench, C Wicking, J Berkman, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|October 17, 2007
Androgen receptor genotyping in a large Australasian cohort with androgen insensitivity syndrome; identification of four novel mutationsY W A Jeske, I N McGown, D M Cowley, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 geneM R Davis, E Haan, H Jungbluth, et al.
American Journal of Human Genetics|June 18, 2005
Deletions involving long-range conserved nongenic sequences upstream and downstream of FOXL2 as a novel disease-causing mechanism in blepharophimosis syndromeD Beysen, J Raes, B P Leroy, et al.
Pageof 2