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W Pretsch

Showing results (31-40 of 38) with videos related to

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Investigative Ophthalmology & Visual Science|December 31, 1997
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16D J Sidjanin, P A Grimes, W Pretsch, et al.
Developmental Biology|March 15, 1996
Purkinje cell lineage and the topographic organization of the cerebellar cortex: a view from X inactivation mosaicsS L Baader, M L Schilling, B Rosengarten, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 1, 1997
Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4E Zhou, P Grimes, J Favor, et al.
Mutation Research|June 1, 1985
Induction of gene mutations in mice: the multiple endpoint approachU H Ehling, D J Charles, J Favor, et al.
Genetical Research|December 1, 1991
The liver/erythrocyte pyruvate kinase gene complex [Pk-1] in the mouse: regulatory gene mutationsL A Fitton, M Davidson, K J Moore, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidneyJ Favor, R Sandulache, A Neuhäuser-Klaus, et al.
Genomics|October 23, 1998
Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genesN Klopp, J Favor, J Löster, et al.
Genomics|June 21, 2001
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi miceD J Sidjanin, D M Parker-Wilson, A Neuhäuser-Klaus, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Investigative Ophthalmology & Visual Science|December 31, 1997
Mapping of the autosomal dominant cataract mutation (Coc) on mouse chromosome 16D J Sidjanin, P A Grimes, W Pretsch, et al.
Developmental Biology|March 15, 1996
Purkinje cell lineage and the topographic organization of the cerebellar cortex: a view from X inactivation mosaicsS L Baader, M L Schilling, B Rosengarten, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|March 1, 1997
Genetic mapping of a mouse ocular malformation locus, Tcm, to chromosome 4E Zhou, P Grimes, J Favor, et al.
Mutation Research|June 1, 1985
Induction of gene mutations in mice: the multiple endpoint approachU H Ehling, D J Charles, J Favor, et al.
Genetical Research|December 1, 1991
The liver/erythrocyte pyruvate kinase gene complex [Pk-1] in the mouse: regulatory gene mutationsL A Fitton, M Davidson, K J Moore, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 26, 1996
The mouse Pax2(1Neu) mutation is identical to a human PAX2 mutation in a family with renal-coloboma syndrome and results in developmental defects of the brain, ear, eye, and kidneyJ Favor, R Sandulache, A Neuhäuser-Klaus, et al.
Genomics|October 23, 1998
Three murine cataract mutants (Cat2) are defective in different gamma-crystallin genesN Klopp, J Favor, J Löster, et al.
Genomics|June 21, 2001
A 76-bp deletion in the Mip gene causes autosomal dominant cataract in Hfi miceD J Sidjanin, D M Parker-Wilson, A Neuhäuser-Klaus, et al.
Pageof 4