Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D M Parry

Showing results (61-70 of 79) with videos related to

Pageof 8
Sort By:
Neurogenetics|February 7, 2001
Allelic expression of the NF2 gene in neurofibromatosis 2 and schwannomatosisL B Jacoby, M MacCollin, D M Parry, et al.
Journal of the National Cancer Institute|April 1, 1982
Carotid body tumors in humans: genetics and epidemiologyD M Parry, F P Li, L C Strong, et al.
Neurogenetics|November 21, 2000
The parental origin of new mutations in neurofibromatosis 2L Kluwe, V Mautner, D M Parry, et al.
The Journal of Endocrinology|July 1, 1989
Photoperiodic control of the development of the LHRH neurosecretory system of European starlings (Sturnus vulgaris) during puberty and the onset of photorefractorinessA R Goldsmith, W E Ivings, A S Pearce-Kelly, et al.
American Journal of Human Genetics|September 1, 1996
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalitiesD M Parry, M M MacCollin, M I Kaiser-Kupfer, et al.
Journal of Medical Genetics|October 1, 1983
Linkage analysis of neurofibromatosis (von Recklinghausen disease)M A Spence, J L Bader, D M Parry, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 1994
In vitro radiosensitivity of fibroblasts from thyroid and skin cancer patients treated with X-rays for tinea capitisE Ron, R E Tarone, B Modan, et al.
American Journal of Human Genetics|September 1, 1992
Neurofibromatosis type 2 appears to be a genetically homogeneous diseaseS A Narod, D M Parry, J Parboosingh, et al.
Somatic Cell and Molecular Genetics|January 27, 1999
Genetic variation in the 3' untranslated region of the neurofibromatosis 1 gene: application to unequal allelic expressionG S Cowley, A E Murthy, D M Parry, et al.
Neurology|September 1, 1993
Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markersM H Ruttledge, S A Narod, J P Dumanski, et al.
Pageof 8

Showing results (61-70 of 79) with videos related to

Sort By:
Pageof 8
Neurogenetics|February 7, 2001
Allelic expression of the NF2 gene in neurofibromatosis 2 and schwannomatosisL B Jacoby, M MacCollin, D M Parry, et al.
Journal of the National Cancer Institute|April 1, 1982
Carotid body tumors in humans: genetics and epidemiologyD M Parry, F P Li, L C Strong, et al.
Neurogenetics|November 21, 2000
The parental origin of new mutations in neurofibromatosis 2L Kluwe, V Mautner, D M Parry, et al.
The Journal of Endocrinology|July 1, 1989
Photoperiodic control of the development of the LHRH neurosecretory system of European starlings (Sturnus vulgaris) during puberty and the onset of photorefractorinessA R Goldsmith, W E Ivings, A S Pearce-Kelly, et al.
American Journal of Human Genetics|September 1, 1996
Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalitiesD M Parry, M M MacCollin, M I Kaiser-Kupfer, et al.
Journal of Medical Genetics|October 1, 1983
Linkage analysis of neurofibromatosis (von Recklinghausen disease)M A Spence, J L Bader, D M Parry, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|April 1, 1994
In vitro radiosensitivity of fibroblasts from thyroid and skin cancer patients treated with X-rays for tinea capitisE Ron, R E Tarone, B Modan, et al.
American Journal of Human Genetics|September 1, 1992
Neurofibromatosis type 2 appears to be a genetically homogeneous diseaseS A Narod, D M Parry, J Parboosingh, et al.
Somatic Cell and Molecular Genetics|January 27, 1999
Genetic variation in the 3' untranslated region of the neurofibromatosis 1 gene: application to unequal allelic expressionG S Cowley, A E Murthy, D M Parry, et al.
Neurology|September 1, 1993
Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markersM H Ruttledge, S A Narod, J P Dumanski, et al.
Pageof 8