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S T Warren

Showing results (1-10 of 108) with videos related to

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American Journal of Human Genetics|January 13, 2000
A new millennium and a new editorS T Warren
Hospital Practice (1995)|April 15, 1997
Trinucleotide repetition and fragile X syndromeS T Warren
Science (New York, N.Y.)|March 8, 1996
The expanding world of trinucleotide repeatsS T Warren
American Journal of Human Genetics|May 1, 1981
Allelism in human oculocutaneous albinismS T Warren
Science (New York, N.Y.)|January 17, 1997
Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13S T Warren
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotypeS T Warren
Seminars in Reproductive Medicine|August 2, 2001
The female and the fragile X reviewedA Kenneson, S T Warren
Human Molecular Genetics|February 28, 1998
Emerin deletions occurring on both Xq28 inversion backgroundsK Small, S T Warren
Human Genetics|November 3, 1998
Polymorphism in the FMR1 geneC Gunter, S T Warren
Human Molecular Genetics|April 18, 2000
Understanding the molecular basis of fragile X syndromeP Jin, S T Warren
Pageof 11

Showing results (1-10 of 108) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|January 13, 2000
A new millennium and a new editorS T Warren
Hospital Practice (1995)|April 15, 1997
Trinucleotide repetition and fragile X syndromeS T Warren
Science (New York, N.Y.)|March 8, 1996
The expanding world of trinucleotide repeatsS T Warren
American Journal of Human Genetics|May 1, 1981
Allelism in human oculocutaneous albinismS T Warren
Science (New York, N.Y.)|January 17, 1997
Polyalanine expansion in synpolydactyly might result from unequal crossing-over of HOXD13S T Warren
American Journal of Medical Genetics|May 1, 1988
Fragile X syndrome: a hypothesis regarding the molecular mechanism of the phenotypeS T Warren
Seminars in Reproductive Medicine|August 2, 2001
The female and the fragile X reviewedA Kenneson, S T Warren
Human Molecular Genetics|February 28, 1998
Emerin deletions occurring on both Xq28 inversion backgroundsK Small, S T Warren
Human Genetics|November 3, 1998
Polymorphism in the FMR1 geneC Gunter, S T Warren
Human Molecular Genetics|April 18, 2000
Understanding the molecular basis of fragile X syndromeP Jin, S T Warren
Pageof 11