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Jeffrey W Innis

Showing results (1-10 of 68) with videos related to

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Teratology|February 22, 2002
Priming the search for HOX mutationsJeffrey W Innis
American Journal of Medical Genetics. Part A|September 25, 2004
Two patients with monomelic ulnar duplication with mirror hand polydactyly: segmental Laurin-Sandrow syndromeJeffrey W Innis, Peter Hedera
American Journal of Medical Genetics. Part A|September 11, 2003
Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical featuresPeter Hedera, Jeffrey W Innis
American Journal of Medical Genetics|July 13, 2002
Possible third case of Lin-Gettig syndromePeter Hedera, Jeffrey W Innis
Transgenic Research|June 6, 2007
A mouse transgene drives embryonic dorsal posterior commissure expressionJessica A Lehoczky, Jeffrey W Innis
Molecular Genetics & Genomic Medicine|May 5, 2018
Interstitial microdeletion of the 1p34.3p34.2 regionJoseph E Jacher, Jeffrey W Innis
Evolution & Development|July 22, 2008
BAC transgenic analysis reveals enhancers sufficient for Hoxa13 and neighborhood gene expression in mouse embryonic distal limbs and genital budJessica A Lehoczky, Jeffrey W Innis
Molecular Genetics and Metabolism|November 19, 2013
Human HOX gene disordersShane C Quinonez, Jeffrey W Innis
Evolution & Development|July 22, 2008
Expanded HOXA13 polyalanine tracts in a monotremeJessica A Lehoczky, Jeffrey W Innis
Nucleic Acids Research|December 3, 2005
A genomic approach to the identification and characterization of HOXA13 functional binding elementsColleen D McCabe, Jeffrey W Innis
Pageof 7

Showing results (1-10 of 68) with videos related to

Sort By:
Pageof 7
Teratology|February 22, 2002
Priming the search for HOX mutationsJeffrey W Innis
American Journal of Medical Genetics. Part A|September 25, 2004
Two patients with monomelic ulnar duplication with mirror hand polydactyly: segmental Laurin-Sandrow syndromeJeffrey W Innis, Peter Hedera
American Journal of Medical Genetics. Part A|September 11, 2003
Juberg-Hayward syndrome: report of a new patient with severe phenotype and novel clinical featuresPeter Hedera, Jeffrey W Innis
American Journal of Medical Genetics|July 13, 2002
Possible third case of Lin-Gettig syndromePeter Hedera, Jeffrey W Innis
Transgenic Research|June 6, 2007
A mouse transgene drives embryonic dorsal posterior commissure expressionJessica A Lehoczky, Jeffrey W Innis
Molecular Genetics & Genomic Medicine|May 5, 2018
Interstitial microdeletion of the 1p34.3p34.2 regionJoseph E Jacher, Jeffrey W Innis
Evolution & Development|July 22, 2008
BAC transgenic analysis reveals enhancers sufficient for Hoxa13 and neighborhood gene expression in mouse embryonic distal limbs and genital budJessica A Lehoczky, Jeffrey W Innis
Molecular Genetics and Metabolism|November 19, 2013
Human HOX gene disordersShane C Quinonez, Jeffrey W Innis
Evolution & Development|July 22, 2008
Expanded HOXA13 polyalanine tracts in a monotremeJessica A Lehoczky, Jeffrey W Innis
Nucleic Acids Research|December 3, 2005
A genomic approach to the identification and characterization of HOXA13 functional binding elementsColleen D McCabe, Jeffrey W Innis
Pageof 7