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M Sarfarazi

Showing results (1-10 of 102) with videos related to

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Human Molecular Genetics|January 1, 1997
Recent advances in molecular genetics of glaucomasM Sarfarazi
Genetic Epidemiology. Supplement|January 1, 1986
Report on genetic linkage analysis between Huntington's disease and the G8 DNA polymorphismM Sarfarazi
Eye (London, England)|October 12, 2000
Molecular genetics of primary congenital glaucomaM Sarfarazi, I Stoilov
Journal of Medical Genetics|February 1, 1986
A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional informationM Sarfarazi, H Williams
The Journal of Pediatrics|April 1, 1997
Family pedigree analysis of children with severe breath-holding spellsF J DiMario, M Sarfarazi
British Medical Journal (Clinical Research Ed.)|June 29, 1985
Genetic prediction and family structure in Huntington's choreaP S Harper, M Sarfarazi
Human Molecular Genetics|April 1, 1997
Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21I Stoilov, A N Akarsu, M Sarfarazi
Angiology|May 4, 1999
Cause of primary congenital lymphedemaA H Child, J Beninson, M Sarfarazi
American Journal of Human Genetics|June 1, 1990
Linkage disequilibrium between two restriction sites in the COL2A1 geneR C Schwartz, M Sarfarazi, P Tsipouras
Journal of Medical Genetics|September 1, 1987
An exclusion map for Von Recklinghausen neurofibromatosisM Sarfarazi, S M Huson, J H Edwards
Pageof 11

Showing results (1-10 of 102) with videos related to

Sort By:
Pageof 11
Human Molecular Genetics|January 1, 1997
Recent advances in molecular genetics of glaucomasM Sarfarazi
Genetic Epidemiology. Supplement|January 1, 1986
Report on genetic linkage analysis between Huntington's disease and the G8 DNA polymorphismM Sarfarazi
Eye (London, England)|October 12, 2000
Molecular genetics of primary congenital glaucomaM Sarfarazi, I Stoilov
Journal of Medical Genetics|February 1, 1986
A computer programme for estimation of genetic risk in X linked disorders, combining pedigree and DNA probe data with other conditional informationM Sarfarazi, H Williams
The Journal of Pediatrics|April 1, 1997
Family pedigree analysis of children with severe breath-holding spellsF J DiMario, M Sarfarazi
British Medical Journal (Clinical Research Ed.)|June 29, 1985
Genetic prediction and family structure in Huntington's choreaP S Harper, M Sarfarazi
Human Molecular Genetics|April 1, 1997
Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (Buphthalmos) in families linked to the GLC3A locus on chromosome 2p21I Stoilov, A N Akarsu, M Sarfarazi
Angiology|May 4, 1999
Cause of primary congenital lymphedemaA H Child, J Beninson, M Sarfarazi
American Journal of Human Genetics|June 1, 1990
Linkage disequilibrium between two restriction sites in the COL2A1 geneR C Schwartz, M Sarfarazi, P Tsipouras
Journal of Medical Genetics|September 1, 1987
An exclusion map for Von Recklinghausen neurofibromatosisM Sarfarazi, S M Huson, J H Edwards
Pageof 11