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M Irving

Showing results (361-370 of 563) with videos related to

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Clinical Genetics|April 27, 2012
Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutationP Kannu, M Nour, M Irving, et al.
Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.
Neuropharmacology|March 20, 2021
Repeated binge ethanol drinking enhances electrical activity of central amygdala corticotropin releasing factor neurons in vivoSonia Aroni, Rosa A M Marino, Kasey S Girven, et al.
Biophysical Journal|July 30, 2003
The conformation of myosin head domains in rigor muscle determined by X-ray interferenceM Reconditi, N Koubassova, M Linari, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
Interference fine structure and sarcomere length dependence of the axial x-ray pattern from active single muscle fibersM Linari, G Piazzesi, I Dobbie, et al.
Journal of Consulting and Clinical Psychology|May 16, 1998
Treatment decision making and adjustment to breast cancer: a longitudinal studyA L Stanton, M A Estes, N C Estes, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|November 23, 2000
Factors predictive of adolescents' intentions to use birth control pills, condoms, and birth control pills in combination with condomsD M Craig, K E Wade, K R Allison, et al.
Biophysical Journal|February 27, 1999
Model-independent analysis of the orientation of fluorescent probes with restricted mobility in muscle fibersR E Dale, S C Hopkins, U A an der Heide, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 1993
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuromaR M Irving, D A Moffat, D G Hardy, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type IaD Coman, D Bostock, M Hunter, et al.
Pageof 57

Showing results (361-370 of 563) with videos related to

Sort By:
Pageof 57
Clinical Genetics|April 27, 2012
Paraspinal ganglioneuroma in the proband of a large family with mild cutaneous manifestations of NF1, carrying a deep NF1 intronic mutationP Kannu, M Nour, M Irving, et al.
Human Molecular Genetics|February 1, 1994
Somatic NF2 gene mutations in familial and non-familial vestibular schwannomaR M Irving, D A Moffat, D G Hardy, et al.
Neuropharmacology|March 20, 2021
Repeated binge ethanol drinking enhances electrical activity of central amygdala corticotropin releasing factor neurons in vivoSonia Aroni, Rosa A M Marino, Kasey S Girven, et al.
Biophysical Journal|July 30, 2003
The conformation of myosin head domains in rigor muscle determined by X-ray interferenceM Reconditi, N Koubassova, M Linari, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 22, 2000
Interference fine structure and sarcomere length dependence of the axial x-ray pattern from active single muscle fibersM Linari, G Piazzesi, I Dobbie, et al.
Journal of Consulting and Clinical Psychology|May 16, 1998
Treatment decision making and adjustment to breast cancer: a longitudinal studyA L Stanton, M A Estes, N C Estes, et al.
Canadian Journal of Public Health = Revue Canadienne De Sante Publique|November 23, 2000
Factors predictive of adolescents' intentions to use birth control pills, condoms, and birth control pills in combination with condomsD M Craig, K E Wade, K R Allison, et al.
Biophysical Journal|February 27, 1999
Model-independent analysis of the orientation of fluorescent probes with restricted mobility in muscle fibersR E Dale, S C Hopkins, U A an der Heide, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 1, 1993
Molecular genetic analysis of the mechanism of tumorigenesis in acoustic neuromaR M Irving, D A Moffat, D G Hardy, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Primary skeletal dysplasia as a major manifesting feature in an infant with congenital disorder of glycosylation type IaD Coman, D Bostock, M Hunter, et al.
Pageof 57