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D M Parry

Showing results (51-60 of 79) with videos related to

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American Journal of Human Genetics|July 14, 2001
Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33M J Kelley, J F Korczak, E Sheridan, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndromeA E Bale, S J Bale, H Murli, et al.
Archives of Internal Medicine|September 9, 1996
Multiple schwannomas and meningiomas associated with irradiation in childhoodL Sznajder, C Abrahams, D M Parry, et al.
American Journal of Medical Genetics|October 1, 1994
Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneityD M Parry, R Eldridge, M I Kaiser-Kupfer, et al.
American Journal of Medical Genetics|August 1, 1986
SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanomaD M Parry, J J Mulvihill, S E Tsai, et al.
Radiology|February 13, 2001
Intramedullary and spinal canal tumors in patients with neurofibromatosis 2: MR imaging findings and correlation with genotypeN J Patronas, N Courcoutsakis, C M Bromley, et al.
Annals of Internal Medicine|July 1, 1990
NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An updateJ J Mulvihill, D M Parry, J L Sherman, et al.
Journal of Medical Genetics|September 1, 1987
Genetic linkage studies with neurofibromatosis: the question of heterogeneityM A Spence, R S Sparkes, D M Parry, et al.
Neuroreport|June 17, 1996
Glutamatergic projections from the rostral hypothalamus to the periaqueductal greyD M Parry, N Johns, F M Semenenko, et al.
Annals of Neurology|September 1, 1996
A point mutation associated with a severe phenotype of neurofibromatosis 2M MacCollin, N Braverman, D Viskochil, et al.
Pageof 8

Showing results (51-60 of 79) with videos related to

Sort By:
Pageof 8
American Journal of Human Genetics|July 14, 2001
Familial chordoma, a tumor of notochordal remnants, is linked to chromosome 7q33M J Kelley, J F Korczak, E Sheridan, et al.
Cancer Genetics and Cytogenetics|October 15, 1989
Sister chromatid exchange and chromosome fragility in the nevoid basal cell carcinoma syndromeA E Bale, S J Bale, H Murli, et al.
Archives of Internal Medicine|September 9, 1996
Multiple schwannomas and meningiomas associated with irradiation in childhoodL Sznajder, C Abrahams, D M Parry, et al.
American Journal of Medical Genetics|October 1, 1994
Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneityD M Parry, R Eldridge, M I Kaiser-Kupfer, et al.
American Journal of Medical Genetics|August 1, 1986
SC phocomelia syndrome, premature centromere separation, and congenital cranial nerve paralysis in two sisters, one with malignant melanomaD M Parry, J J Mulvihill, S E Tsai, et al.
Radiology|February 13, 2001
Intramedullary and spinal canal tumors in patients with neurofibromatosis 2: MR imaging findings and correlation with genotypeN J Patronas, N Courcoutsakis, C M Bromley, et al.
Annals of Internal Medicine|July 1, 1990
NIH conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An updateJ J Mulvihill, D M Parry, J L Sherman, et al.
Journal of Medical Genetics|September 1, 1987
Genetic linkage studies with neurofibromatosis: the question of heterogeneityM A Spence, R S Sparkes, D M Parry, et al.
Neuroreport|June 17, 1996
Glutamatergic projections from the rostral hypothalamus to the periaqueductal greyD M Parry, N Johns, F M Semenenko, et al.
Annals of Neurology|September 1, 1996
A point mutation associated with a severe phenotype of neurofibromatosis 2M MacCollin, N Braverman, D Viskochil, et al.
Pageof 8