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H Brauch

Showing results (41-50 of 72) with videos related to

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Nucleic Acids Research|February 25, 1990
A new polymorphic probe on chromosome 3p: lambda LIB31-57' (D3S213)F Latif, G M Glenn, L N Daniel, et al.
Journal of the National Cancer Institute|July 19, 1989
Specific genetic change in tumors associated with von Hippel-Lindau diseaseK Tory, H Brauch, M Linehan, et al.
Human Genetics|May 1, 1995
Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effectH Brauch, T Kishida, D Glavac, et al.
Nucleic Acids Research|March 25, 1990
A new polymorphic probe on chromosome 3p: lambda LIB45-82 (D3S232)F Latif, G M Glenn, L N Daniel, et al.
Nucleic Acids Research|January 11, 1990
A new polymorphic probe on chromosome 3p: lambda LIB49-63 (D3S192E)M I Lerman, G M Glenn, F Latif, et al.
Nucleic Acids Research|February 25, 1990
A new polymorphic probe on chromosome 3p: lambda LIB28-56'' (D3S207)F Latif, G M Glenn, L N Daniel, et al.
Cancer Research|February 15, 1991
Molecular analysis of genetic changes in the origin and development of renal cell carcinomaP Anglard, K Tory, H Brauch, et al.
Nucleic Acids Research|January 11, 1990
A new polymorphic probe on chromosome 3p: lambda LIB28-77 (D3S169E)M I Lerman, G M Glenn, L Daniel, et al.
JAMA|October 11, 1995
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type IIH P Neumann, C Eng, L M Mulligan, et al.
Human Genetics|June 1, 1996
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGHH J Decker, C Neuhaus, A Jauch, et al.
Pageof 8

Showing results (41-50 of 72) with videos related to

Sort By:
Pageof 8
Nucleic Acids Research|February 25, 1990
A new polymorphic probe on chromosome 3p: lambda LIB31-57' (D3S213)F Latif, G M Glenn, L N Daniel, et al.
Journal of the National Cancer Institute|July 19, 1989
Specific genetic change in tumors associated with von Hippel-Lindau diseaseK Tory, H Brauch, M Linehan, et al.
Human Genetics|May 1, 1995
Von Hippel-Lindau (VHL) disease with pheochromocytoma in the Black Forest region of Germany: evidence for a founder effectH Brauch, T Kishida, D Glavac, et al.
Nucleic Acids Research|March 25, 1990
A new polymorphic probe on chromosome 3p: lambda LIB45-82 (D3S232)F Latif, G M Glenn, L N Daniel, et al.
Nucleic Acids Research|January 11, 1990
A new polymorphic probe on chromosome 3p: lambda LIB49-63 (D3S192E)M I Lerman, G M Glenn, F Latif, et al.
Nucleic Acids Research|February 25, 1990
A new polymorphic probe on chromosome 3p: lambda LIB28-56'' (D3S207)F Latif, G M Glenn, L N Daniel, et al.
Cancer Research|February 15, 1991
Molecular analysis of genetic changes in the origin and development of renal cell carcinomaP Anglard, K Tory, H Brauch, et al.
Nucleic Acids Research|January 11, 1990
A new polymorphic probe on chromosome 3p: lambda LIB28-77 (D3S169E)M I Lerman, G M Glenn, L Daniel, et al.
JAMA|October 11, 1995
Consequences of direct genetic testing for germline mutations in the clinical management of families with multiple endocrine neoplasia, type IIH P Neumann, C Eng, L M Mulligan, et al.
Human Genetics|June 1, 1996
Detection of a germline mutation and somatic homozygous loss of the von Hippel-Lindau tumor-suppressor gene in a family with a de novo mutation. A combined genetic study, including cytogenetics, PCR/SSCP, FISH, and CGHH J Decker, C Neuhaus, A Jauch, et al.
Pageof 8