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J H Smith

Showing results (351-360 of 588) with videos related to

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BMC Genomics|November 15, 2012
Pre-capture multiplexing improves efficiency and cost-effectiveness of targeted genomic enrichmentA Eliot Shearer, Michael S Hildebrand, Harini Ravi, et al.
BMC Medical Genomics|June 15, 2023
Single-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4<sup>-/-</sup> mouseJin-Young Koh, Corentin Affortit, Paul T Ranum, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Did the GJB2 35delG mutation originate in Iran?Vahideh Norouzi, Hiva Azizi, Zohreh Fattahi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2008
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locusMichael S Hildebrand, Dylan Tack, Sarah J McMordie, et al.
British Journal of Obstetrics and Gynaecology|October 1, 1988
Antenatal fetal heart rate variation in relation to the respiratory and metabolic status of the compromised human fetusJ H Smith, K J Anand, P M Cotes, et al.
Archives of Otolaryngology--Head & Neck Surgery|October 9, 2002
Treatment of lymphangiomas with OK-432 (Picibanil) sclerotherapy: a prospective multi-institutional trialChantal M Giguère, Nancy M Bauman, Yutaka Sato, et al.
American Journal of Medical Genetics. Part A|April 11, 2012
COL1A1 association and otosclerosis: a meta-analysisIsabelle Schrauwen, Ayda Khalfallah, Megan Ealy, et al.
Kidney International|June 8, 2012
C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-upSanjeev Sethi, Fernando C Fervenza, Yuzhou Zhang, et al.
The Annals of Otology, Rhinology, and Laryngology|October 26, 2005
HspE7 treatment of pediatric recurrent respiratory papillomatosis: final results of an open-label trialCraig S Derkay, Richard J H Smith, John McClay, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 23, 2008
Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipientMicah R Chan, Christie P Thomas, Jose R Torrealba, et al.
Pageof 59

Showing results (351-360 of 588) with videos related to

Sort By:
Pageof 59
BMC Genomics|November 15, 2012
Pre-capture multiplexing improves efficiency and cost-effectiveness of targeted genomic enrichmentA Eliot Shearer, Michael S Hildebrand, Harini Ravi, et al.
BMC Medical Genomics|June 15, 2023
Single-cell RNA-sequencing of stria vascularis cells in the adult Slc26a4<sup>-/-</sup> mouseJin-Young Koh, Corentin Affortit, Paul T Ranum, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Did the GJB2 35delG mutation originate in Iran?Vahideh Norouzi, Hiva Azizi, Zohreh Fattahi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 23, 2008
Audioprofile-directed screening identifies novel mutations in KCNQ4 causing hearing loss at the DFNA2 locusMichael S Hildebrand, Dylan Tack, Sarah J McMordie, et al.
British Journal of Obstetrics and Gynaecology|October 1, 1988
Antenatal fetal heart rate variation in relation to the respiratory and metabolic status of the compromised human fetusJ H Smith, K J Anand, P M Cotes, et al.
Archives of Otolaryngology--Head & Neck Surgery|October 9, 2002
Treatment of lymphangiomas with OK-432 (Picibanil) sclerotherapy: a prospective multi-institutional trialChantal M Giguère, Nancy M Bauman, Yutaka Sato, et al.
American Journal of Medical Genetics. Part A|April 11, 2012
COL1A1 association and otosclerosis: a meta-analysisIsabelle Schrauwen, Ayda Khalfallah, Megan Ealy, et al.
Kidney International|June 8, 2012
C3 glomerulonephritis: clinicopathological findings, complement abnormalities, glomerular proteomic profile, treatment, and follow-upSanjeev Sethi, Fernando C Fervenza, Yuzhou Zhang, et al.
The Annals of Otology, Rhinology, and Laryngology|October 26, 2005
HspE7 treatment of pediatric recurrent respiratory papillomatosis: final results of an open-label trialCraig S Derkay, Richard J H Smith, John McClay, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 23, 2008
Recurrent atypical hemolytic uremic syndrome associated with factor I mutation in a living related renal transplant recipientMicah R Chan, Christie P Thomas, Jose R Torrealba, et al.
Pageof 59