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G Newman

Showing results (751-760 of 934) with videos related to

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European Journal of Human Genetics : EJHG|June 16, 2016
Spectrum of PEX1 and PEX6 variants in Heimler syndromeClaire E L Smith, James A Poulter, Alex V Levin, et al.
European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.
Head & Neck|May 5, 2016
Endoscopy versus imaging: Analysis of surveillance methods in sinonasal malignancySammy Khalili, Douglas M Worrall, Steve Brooks, et al.
Kidney International Reports|July 13, 2023
Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder DiseaseCeline Grenier, Filipa M Lopes, Anna M Cueto-González, et al.
Arthritis and Rheumatism|November 30, 2006
Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian populationWilliam G Newman, Qing Zhang, Xiangdong Liu, et al.
The Laryngoscope|July 5, 2020
Retropharyngeal Internal Carotid Artery Management in TORS Using Microvascular ReconstructionHarman S Parhar, Robert M Brody, David Shimunov, et al.
Cancers|August 27, 2021
Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior <i>BRCA1/2</i> ProbabilityD Gareth Evans, Elke M van Veen, Emma R Woodward, et al.
The Medical Journal of Australia|May 2, 2020
Consensus statement: Safe Airway Society principles of airway management and tracheal intubation specific to the COVID-19 adult patient groupDavid J Brewster, Nicholas Chrimes, Thy Bt Do, 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|August 24, 2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder diseaseGlenda M Beaman, Gabriella Galatà, Keng W Teik, et al.
Pageof 94

Showing results (751-760 of 934) with videos related to

Sort By:
Pageof 94
European Journal of Human Genetics : EJHG|June 16, 2016
Spectrum of PEX1 and PEX6 variants in Heimler syndromeClaire E L Smith, James A Poulter, Alex V Levin, et al.
European Journal of Medical Genetics|June 15, 2020
Ligase IV syndrome can present with microcephaly and radial ray anomalies similar to Fanconi anaemia plus fatal kidney malformationsRajesh Madhu, Glenda M Beaman, Kate E Chandler, et al.
Head & Neck|May 5, 2016
Endoscopy versus imaging: Analysis of surveillance methods in sinonasal malignancySammy Khalili, Douglas M Worrall, Steve Brooks, et al.
Kidney International Reports|July 13, 2023
Neurogenic Defects Occur in <i>LRIG2</i>-Associated Urinary Bladder DiseaseCeline Grenier, Filipa M Lopes, Anna M Cueto-González, et al.
Arthritis and Rheumatism|November 30, 2006
Rheumatoid arthritis association with the FCRL3 -169C polymorphism is restricted to PTPN22 1858T-homozygous individuals in a Canadian populationWilliam G Newman, Qing Zhang, Xiangdong Liu, et al.
The Laryngoscope|July 5, 2020
Retropharyngeal Internal Carotid Artery Management in TORS Using Microvascular ReconstructionHarman S Parhar, Robert M Brody, David Shimunov, et al.
Cancers|August 27, 2021
Gene Panel Testing for Breast Cancer Reveals Differential Effect of Prior <i>BRCA1/2</i> ProbabilityD Gareth Evans, Elke M van Veen, Emma R Woodward, et al.
The Medical Journal of Australia|May 2, 2020
Consensus statement: Safe Airway Society principles of airway management and tracheal intubation specific to the COVID-19 adult patient groupDavid J Brewster, Nicholas Chrimes, Thy Bt Do, 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|August 24, 2019
A homozygous missense variant in CHRM3 associated with familial urinary bladder diseaseGlenda M Beaman, Gabriella Galatà, Keng W Teik, et al.
Pageof 94