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W Scherer

Showing results (321-330 of 915) with videos related to

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American Journal of Medical Genetics. Part A|February 5, 2003
Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locusErwin Petek, Christian Windpassinger, Monika Mach, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|November 21, 2012
Exercise interventions on health-related quality of life for people with cancer during active treatmentShiraz I Mishra, Roberta W Scherer, Claire Snyder, et al.
Annals of Neurology|May 11, 2000
X-linked vacuolar myopathies: two separate loci and refined genetic mappingM Auranen, M Villanova, F Muntoni, et al.
The Cochrane Database of Systematic Reviews|August 17, 2012
Exercise interventions on health-related quality of life for people with cancer during active treatmentShiraz I Mishra, Roberta W Scherer, Claire Snyder, et al.
JAMA Psychiatry|December 1, 2021
Deletion of Loss-of-Function-Intolerant Genes and Risk of 5 Psychiatric DisordersMichael Wainberg, Daniele Merico, Guillaume Huguet, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|March 1, 1988
Numerical and experimental study of steady-state CO2 and inert gas washoutP W Scherer, S Gobran, S J Aukburg, et al.
Human Molecular Genetics|September 23, 2008
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndromeAnne S Bassett, Christian R Marshall, Anath C Lionel, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial featuresBrian H Y Chung, James Stavropoulos, Christian R Marshall, et al.
Genomics|January 15, 1996
Fine mapping of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer proteinK Takahara, L Osborne, R W Elliott, et al.
Pediatric Neurology|August 14, 2012
Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsyDanielle M Andrade, Tara Paton, Julie Turnbull, et al.
Pageof 92

Showing results (321-330 of 915) with videos related to

Sort By:
Pageof 92
American Journal of Medical Genetics. Part A|February 5, 2003
Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locusErwin Petek, Christian Windpassinger, Monika Mach, et al.
Clinical Otolaryngology : Official Journal of ENT-UK ; Official Journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery|November 21, 2012
Exercise interventions on health-related quality of life for people with cancer during active treatmentShiraz I Mishra, Roberta W Scherer, Claire Snyder, et al.
Annals of Neurology|May 11, 2000
X-linked vacuolar myopathies: two separate loci and refined genetic mappingM Auranen, M Villanova, F Muntoni, et al.
The Cochrane Database of Systematic Reviews|August 17, 2012
Exercise interventions on health-related quality of life for people with cancer during active treatmentShiraz I Mishra, Roberta W Scherer, Claire Snyder, et al.
JAMA Psychiatry|December 1, 2021
Deletion of Loss-of-Function-Intolerant Genes and Risk of 5 Psychiatric DisordersMichael Wainberg, Daniele Merico, Guillaume Huguet, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|March 1, 1988
Numerical and experimental study of steady-state CO2 and inert gas washoutP W Scherer, S Gobran, S J Aukburg, et al.
Human Molecular Genetics|September 23, 2008
Copy number variations and risk for schizophrenia in 22q11.2 deletion syndromeAnne S Bassett, Christian R Marshall, Anath C Lionel, et al.
American Journal of Medical Genetics. Part A|January 29, 2011
2q23 de novo microdeletion involving the MBD5 gene in a patient with developmental delay, postnatal microcephaly and distinct facial featuresBrian H Y Chung, James Stavropoulos, Christian R Marshall, et al.
Genomics|January 15, 1996
Fine mapping of the human and mouse genes for the type I procollagen COOH-terminal proteinase enhancer proteinK Takahara, L Osborne, R W Elliott, et al.
Pediatric Neurology|August 14, 2012
Mutation of the CLN6 gene in teenage-onset progressive myoclonus epilepsyDanielle M Andrade, Tara Paton, Julie Turnbull, et al.
Pageof 92