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C Morton

Showing results (681-690 of 853) with videos related to

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Hearing Research|February 5, 2008
Expression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient miceRobin E Williamson, Keith N Darrow, Anne B S Giersch, et al.
Prenatal Diagnosis|July 22, 2014
Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencingM J Macera, A Sobrino, B Levy, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|December 5, 2019
Inhibition of ATP hydrolysis restores airway surface liquid production in cystic fibrosis airway epitheliaCatharina van Heusden, Brian Button, Wayne H Anderson, et al.
American Journal of Human Genetics|October 1, 2019
GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK BiobankHelena R R Wells, Maxim B Freidin, Fatin N Zainul Abidin, et al.
Current Protocols in Human Genetics|October 5, 2010
Reporting of diagnostic cytogenetic resultsAzra H Ligon, Cynthia C Morton, Frederick R Bieber, et al.
Current Protocols in Human Genetics|July 8, 2011
Reporting of diagnostic cytogenetic resultsAzra H Ligon, Cynthia C Morton, Frederick R Bieber, et al.
Journal of Medical Genetics|August 3, 2005
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1H G Kim, S R Herrick, E Lemyre, et al.
Head and Neck Pathology|September 8, 2019
First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding CochlinAtreyee Basu, Nicole J Boczek, Nahid G Robertson, et al.
Human Molecular Genetics|August 14, 2008
A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunctionNahid G Robertson, Sherri M Jones, Theru A Sivakumaran, et al.
Journal of Clinical Epidemiology|July 20, 2017
AHRQ series on complex intervention systematic reviews-paper 4: selecting analytic approachesMeera Viswanathan, Melissa L McPheeters, M Hassan Murad, et al.
Pageof 86

Showing results (681-690 of 853) with videos related to

Sort By:
Pageof 86
Hearing Research|February 5, 2008
Expression studies of osteoglycin/mimecan (OGN) in the cochlea and auditory phenotype of Ogn-deficient miceRobin E Williamson, Keith N Darrow, Anne B S Giersch, et al.
Prenatal Diagnosis|July 22, 2014
Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole-genome sequencingM J Macera, A Sobrino, B Levy, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|December 5, 2019
Inhibition of ATP hydrolysis restores airway surface liquid production in cystic fibrosis airway epitheliaCatharina van Heusden, Brian Button, Wayne H Anderson, et al.
American Journal of Human Genetics|October 1, 2019
GWAS Identifies 44 Independent Associated Genomic Loci for Self-Reported Adult Hearing Difficulty in UK BiobankHelena R R Wells, Maxim B Freidin, Fatin N Zainul Abidin, et al.
Current Protocols in Human Genetics|October 5, 2010
Reporting of diagnostic cytogenetic resultsAzra H Ligon, Cynthia C Morton, Frederick R Bieber, et al.
Current Protocols in Human Genetics|July 8, 2011
Reporting of diagnostic cytogenetic resultsAzra H Ligon, Cynthia C Morton, Frederick R Bieber, et al.
Journal of Medical Genetics|August 3, 2005
Hypogonadotropic hypogonadism and cleft lip and palate caused by a balanced translocation producing haploinsufficiency for FGFR1H G Kim, S R Herrick, E Lemyre, et al.
Head and Neck Pathology|September 8, 2019
First Report of Bilateral External Auditory Canal Cochlin Aggregates ("Cochlinomas") with Multifocal Amyloid-Like Deposits, Associated with Sensorineural Hearing Loss and a Novel Genetic Variant in COCH Encoding CochlinAtreyee Basu, Nicole J Boczek, Nahid G Robertson, et al.
Human Molecular Genetics|August 14, 2008
A targeted Coch missense mutation: a knock-in mouse model for DFNA9 late-onset hearing loss and vestibular dysfunctionNahid G Robertson, Sherri M Jones, Theru A Sivakumaran, et al.
Journal of Clinical Epidemiology|July 20, 2017
AHRQ series on complex intervention systematic reviews-paper 4: selecting analytic approachesMeera Viswanathan, Melissa L McPheeters, M Hassan Murad, et al.
Pageof 86