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R Forman

Showing results (331-340 of 337) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Thorax|April 6, 2018
Fibrinogen does not relate to cardiovascular or muscle manifestations in COPD: cross-sectional data from the ERICA studyDivya Mohan, Julia R Forman, Matthew Allinder, et al.
Clinical Endocrinology|August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidismHakan Cangul, Neil V Morgan, Julia R Forman, et al.
Human Mutation|October 6, 2009
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHDChristopher J Ricketts, Julia R Forman, Eleanor Rattenberry, et al.
CERN Ideasquare Journal of Experimental Innovation|November 28, 2017
Applying physical science techniques and CERN technology to an unsolved problem in radiation treatment for cancer: the multidisciplinary 'VoxTox' research programmeNeil G Burnet, Jessica E Scaife, Marina Romanchikova, et al.
Nature|August 17, 2012
A massive, cooling-flow-induced starburst in the core of a luminous cluster of galaxiesM McDonald, M Bayliss, B A Benson, et al.
Diagnostic and Prognostic Research|May 17, 2019
Erratum to: Methods for evaluating medical tests and biomarkersGowri Gopalakrishna, Miranda Langendam, Rob Scholten, et al.
Pageof 34

Showing results (331-340 of 337) with videos related to

Sort By:
Pageof 34
You have reached the last page of results.This site can display upto 337 results.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesisHakan Cangul, Zehra Aycan, Halil Saglam, et al.
Thorax|April 6, 2018
Fibrinogen does not relate to cardiovascular or muscle manifestations in COPD: cross-sectional data from the ERICA studyDivya Mohan, Julia R Forman, Matthew Allinder, et al.
Clinical Endocrinology|August 20, 2010
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidismHakan Cangul, Neil V Morgan, Julia R Forman, et al.
Human Mutation|October 6, 2009
Tumor risks and genotype-phenotype-proteotype analysis in 358 patients with germline mutations in SDHB and SDHDChristopher J Ricketts, Julia R Forman, Eleanor Rattenberry, et al.
CERN Ideasquare Journal of Experimental Innovation|November 28, 2017
Applying physical science techniques and CERN technology to an unsolved problem in radiation treatment for cancer: the multidisciplinary 'VoxTox' research programmeNeil G Burnet, Jessica E Scaife, Marina Romanchikova, et al.
Nature|August 17, 2012
A massive, cooling-flow-induced starburst in the core of a luminous cluster of galaxiesM McDonald, M Bayliss, B A Benson, et al.
Diagnostic and Prognostic Research|May 17, 2019
Erratum to: Methods for evaluating medical tests and biomarkersGowri Gopalakrishna, Miranda Langendam, Rob Scholten, et al.
Pageof 34