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M A Walter

Showing results (71-80 of 88) with videos related to

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Human Molecular Genetics|August 7, 2001
Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndromeM Priston, K Kozlowski, D Gill, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1991
Ig H chain variable and C region genes in common variable immunodeficiency. Characterization of two new deletion haplotypesP G Olsson, M H Hofker, M A Walter, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 1, 1996
Fibroblast growth factor-induced motor end plate regeneration in atrophic muscleM A Walter, D M Toriumi, B S Patt, et al.
Human Genetics|December 18, 1998
Chromosomal localization and genomic organization of the human retinal rod Na-Ca+K exchangerJ E Tucker, R J Winkfein, S K Murthy, et al.
Developmental Biology|September 10, 1999
Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null allelesG E Winnier, T Kume, K Deng, et al.
Journal of Medical Genetics|June 14, 2001
Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomalyA Vincent, G Billingsley, M Priston, et al.
American Journal of Otolaryngology|May 1, 1995
Size/shape analysis of aerodigestive foreign bodies in children: a multi-institutional studyJ S Reilly, M A Walter, D Beste, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1988
Physical linkage of a human immunoglobulin heavy chain variable region gene segment to diversity and joining region elementsH W Schroeder, M A Walter, M H Hofker, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Report of the second international workshop on human chromosome 14 mapping 1994D W Cox, T Gedde-Dahl, A G Menon, et al.
Pageof 9

Showing results (71-80 of 88) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|August 7, 2001
Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndromeM Priston, K Kozlowski, D Gill, et al.
European Journal of Human Genetics : EJHG|March 14, 2000
Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25F Mirzayans, D B Gould, E Héon, et al.
Journal of Immunology (Baltimore, Md. : 1950)|October 15, 1991
Ig H chain variable and C region genes in common variable immunodeficiency. Characterization of two new deletion haplotypesP G Olsson, M H Hofker, M A Walter, et al.
Archives of Otolaryngology--Head & Neck Surgery|April 1, 1996
Fibroblast growth factor-induced motor end plate regeneration in atrophic muscleM A Walter, D M Toriumi, B S Patt, et al.
Human Genetics|December 18, 1998
Chromosomal localization and genomic organization of the human retinal rod Na-Ca+K exchangerJ E Tucker, R J Winkfein, S K Murthy, et al.
Developmental Biology|September 10, 1999
Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null allelesG E Winnier, T Kume, K Deng, et al.
Journal of Medical Genetics|June 14, 2001
Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomalyA Vincent, G Billingsley, M Priston, et al.
American Journal of Otolaryngology|May 1, 1995
Size/shape analysis of aerodigestive foreign bodies in children: a multi-institutional studyJ S Reilly, M A Walter, D Beste, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 1, 1988
Physical linkage of a human immunoglobulin heavy chain variable region gene segment to diversity and joining region elementsH W Schroeder, M A Walter, M H Hofker, et al.
Cytogenetics and Cell Genetics|January 1, 1995
Report of the second international workshop on human chromosome 14 mapping 1994D W Cox, T Gedde-Dahl, A G Menon, et al.
Pageof 9