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N C Meyer

Showing results (1-10 of 11) with videos related to

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United States Naval Medical Bulletin|March 19, 2010
Guillotine amputation modified to preserve skin flapsN C MEYER
Plant Physiology|January 1, 1995
Nucleotide sequence of a gene encoding a 58.5-kilodalton barley dehydrin that lacks a serine tractT J Close, N C Meyer, J Radik
Protein Expression and Purification|June 1, 1994
Purification of a maize dehydrinT L Ceccardi, N C Meyer, T J Close
Clinical Genetics|July 31, 2007
Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigreeN C Meyer, C J Nishimura, S McMordie, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1978
Effect of thyroid hormones on the prolactin response to thyrotropin-releasing hormone in normal persons and euthyroid goitrous patientsH E Carlson, C T Sawin, L G Krugman, et al.
Genome Research|May 1, 1997
Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22P Lauer, N C Meyer, C E Prass, et al.
Journal of Medical Genetics|July 22, 2005
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locusW Chen, K Kahrizi, N C Meyer, et al.
Gene|March 14, 2001
Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locusN Kasai, K Fukushima, Y Ueki, et al.
Clinical Genetics|May 11, 2007
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisW Chen, N C Meyer, M J McKenna, et al.
Genome Research|May 1, 1997
A 1.1-Mb transcript map of the hereditary hemochromatosis locusD A Ruddy, G S Kronmal, V K Lee, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
United States Naval Medical Bulletin|March 19, 2010
Guillotine amputation modified to preserve skin flapsN C MEYER
Plant Physiology|January 1, 1995
Nucleotide sequence of a gene encoding a 58.5-kilodalton barley dehydrin that lacks a serine tractT J Close, N C Meyer, J Radik
Protein Expression and Purification|June 1, 1994
Purification of a maize dehydrinT L Ceccardi, N C Meyer, T J Close
Clinical Genetics|July 31, 2007
Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigreeN C Meyer, C J Nishimura, S McMordie, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1978
Effect of thyroid hormones on the prolactin response to thyrotropin-releasing hormone in normal persons and euthyroid goitrous patientsH E Carlson, C T Sawin, L G Krugman, et al.
Genome Research|May 1, 1997
Clone-contig and STS maps of the hereditary hemochromatosis region on human chromosome 6p21.3-p22P Lauer, N C Meyer, C E Prass, et al.
Journal of Medical Genetics|July 22, 2005
Mutation of COL11A2 causes autosomal recessive non-syndromic hearing loss at the DFNB53 locusW Chen, K Kahrizi, N C Meyer, et al.
Gene|March 14, 2001
Genomic structures of SCN2A and SCN3A - candidate genes for deafness at the DFNA16 locusN Kasai, K Fukushima, Y Ueki, et al.
Clinical Genetics|May 11, 2007
Single-nucleotide polymorphisms in the COL1A1 regulatory regions are associated with otosclerosisW Chen, N C Meyer, M J McKenna, et al.
Genome Research|May 1, 1997
A 1.1-Mb transcript map of the hereditary hemochromatosis locusD A Ruddy, G S Kronmal, V K Lee, et al.
Pageof 2