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C G Mathew

Showing results (81-90 of 129) with videos related to

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Klinische Wochenschrift|September 15, 1989
Early diagnosis of multiple endocrine neoplasia type IIaH P Neumann, O A Müller, B A Ponder, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1990
[Diagnosis of multiple endocrine neoplasms type IIa using DNA analysis]H P Neumann, O A Müller, B A Ponder, et al.
Human Mutation|February 6, 1998
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstreamJ R Lo Ten Foe, F A Kruyt, M B Zweekhorst, et al.
The Journal of Investigative Dermatology|October 3, 1999
Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresisN V Whittock, G H Ashton, R Mohammedi, et al.
Genomics|August 1, 1989
Linked markers flanking the gene for multiple endocrine neoplasia type 2AY Nakamura, C G Mathew, H Sobol, et al.
Experimental Hematology|April 21, 1999
A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulationG Kupfer, D Naf, I Garcia-Higuera, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|April 1, 1990
Application of linked DNA markers to screening families with multiple endocrine neoplasia type 2AH Telenius, C G Mathew, Y Nakamura, et al.
Leukemia|January 30, 2004
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemiaM D Tischkowitz, N V Morgan, D Grimwade, et al.
American Journal of Human Genetics|July 1, 1996
Analysis of the contribution of HLA genes to genetic predisposition in inflammatory bowel diseaseI Naom, J Lee, D Ford, et al.
Nature|February 8, 1990
Paternal origin of new mutations in von Recklinghausen neurofibromatosisD Jadayel, P Fain, M Upadhyaya, et al.
Pageof 13

Showing results (81-90 of 129) with videos related to

Sort By:
Pageof 13
Klinische Wochenschrift|September 15, 1989
Early diagnosis of multiple endocrine neoplasia type IIaH P Neumann, O A Müller, B A Ponder, et al.
Verhandlungen Der Deutschen Gesellschaft Fur Pathologie|January 1, 1990
[Diagnosis of multiple endocrine neoplasms type IIa using DNA analysis]H P Neumann, O A Müller, B A Ponder, et al.
Human Mutation|February 6, 1998
Exon 6 skipping in the Fanconi anemia C gene associated with a nonsense/missense mutation (775C-->T) in exon 5: the first example of a nonsense mutation in one exon causing skipping of another downstreamJ R Lo Ten Foe, F A Kruyt, M B Zweekhorst, et al.
The Journal of Investigative Dermatology|October 3, 1999
Comparative mutation detection screening of the type VII collagen gene (COL7A1) using the protein truncation test, fluorescent chemical cleavage of mismatch, and conformation sensitive gel electrophoresisN V Whittock, G H Ashton, R Mohammedi, et al.
Genomics|August 1, 1989
Linked markers flanking the gene for multiple endocrine neoplasia type 2AY Nakamura, C G Mathew, H Sobol, et al.
Experimental Hematology|April 21, 1999
A patient-derived mutant form of the Fanconi anemia protein, FANCA, is defective in nuclear accumulationG Kupfer, D Naf, I Garcia-Higuera, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|April 1, 1990
Application of linked DNA markers to screening families with multiple endocrine neoplasia type 2AH Telenius, C G Mathew, Y Nakamura, et al.
Leukemia|January 30, 2004
Deletion and reduced expression of the Fanconi anemia FANCA gene in sporadic acute myeloid leukemiaM D Tischkowitz, N V Morgan, D Grimwade, et al.
American Journal of Human Genetics|July 1, 1996
Analysis of the contribution of HLA genes to genetic predisposition in inflammatory bowel diseaseI Naom, J Lee, D Ford, et al.
Nature|February 8, 1990
Paternal origin of new mutations in von Recklinghausen neurofibromatosisD Jadayel, P Fain, M Upadhyaya, et al.
Pageof 13