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

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Science (New York, N.Y.)|April 17, 1987
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosisB R Seizinger, G Rouleau, L J Ozelius, et al.
Journal of Medical Genetics|December 1, 1990
A 90 kb DNA deletion associated with neurofibromatosis type 1M Upadhyaya, A Cheryson, W Broadhead, et al.
Journal of Medical Genetics|September 1, 1987
Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genesR E Ferrell, K H Buetow, J K Darby, et al.
Journal of Medical Genetics|September 1, 1987
DNA linkage analysis in Von Recklinghausen neurofibromatosisB R Seizinger, G Rouleau, A H Lane, et al.
Cell|June 5, 1987
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor geneB R Seizinger, G A Rouleau, L J Ozelius, et al.
Human Molecular Genetics|April 18, 1998
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutationD J Marsh, V Coulon, K L Lunetta, 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.
Science (New York, N.Y.)|April 17, 1987
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosisB R Seizinger, G Rouleau, L J Ozelius, et al.
Journal of Medical Genetics|December 1, 1990
A 90 kb DNA deletion associated with neurofibromatosis type 1M Upadhyaya, A Cheryson, W Broadhead, et al.
Journal of Medical Genetics|September 1, 1987
Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genesR E Ferrell, K H Buetow, J K Darby, et al.
Journal of Medical Genetics|September 1, 1987
DNA linkage analysis in Von Recklinghausen neurofibromatosisB R Seizinger, G Rouleau, A H Lane, et al.
Cell|June 5, 1987
Genetic linkage of von Recklinghausen neurofibromatosis to the nerve growth factor receptor geneB R Seizinger, G A Rouleau, L J Ozelius, et al.
Human Molecular Genetics|April 18, 1998
Mutation spectrum and genotype-phenotype analyses in Cowden disease and Bannayan-Zonana syndrome, two hamartoma syndromes with germline PTEN mutationD J Marsh, V Coulon, K L Lunetta, et al.
Pageof 2