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W G Newman

Showing results (21-30 of 28) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|July 9, 2010
Novel corticosteroid-binding globulin variant that lacks steroid binding activityI Perogamvros, C Underhill, D E Henley, et al.
Journal of Medical Genetics|February 21, 2008
Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosisK D Hadfield, W G Newman, N L Bowers, et al.
Oncogene|August 24, 2010
Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomasK D Hadfield, M J Smith, J E Urquhart, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Clinical Genetics|January 13, 2016
DMRTA2 (DMRT5) is mutated in a novel cortical brain malformationJ E Urquhart, G Beaman, H Byers, et al.
Clinical Genetics|March 13, 2016
Expanding the genotypic spectrum of Perrault syndromeL A M Demain, J E Urquhart, J O'Sullivan, et al.
Journal of Medical Genetics|August 19, 2007
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohortsB L Browning, V Annese, M L Barclay, et al.
Clinical Pharmacology and Therapeutics|September 25, 2013
CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populationsM A Province, M P Goetz, H Brauch, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
The Journal of Clinical Endocrinology and Metabolism|July 9, 2010
Novel corticosteroid-binding globulin variant that lacks steroid binding activityI Perogamvros, C Underhill, D E Henley, et al.
Journal of Medical Genetics|February 21, 2008
Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosisK D Hadfield, W G Newman, N L Bowers, et al.
Oncogene|August 24, 2010
Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomasK D Hadfield, M J Smith, J E Urquhart, et al.
Clinical Genetics|September 16, 2016
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndromeR Faridi, A U Rehman, R J Morell, et al.
Clinical Genetics|January 13, 2016
DMRTA2 (DMRT5) is mutated in a novel cortical brain malformationJ E Urquhart, G Beaman, H Byers, et al.
Clinical Genetics|March 13, 2016
Expanding the genotypic spectrum of Perrault syndromeL A M Demain, J E Urquhart, J O'Sullivan, et al.
Journal of Medical Genetics|August 19, 2007
Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohortsB L Browning, V Annese, M L Barclay, et al.
Clinical Pharmacology and Therapeutics|September 25, 2013
CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populationsM A Province, M P Goetz, H Brauch, et al.
Pageof 3