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Chad A Shaw

Showing results (71-80 of 172) with videos related to

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The Journal of Allergy and Clinical Immunology|November 19, 2019
Increased Moraxella and Streptococcus species abundance after severe bronchiolitis is associated with recurrent wheezingJonathan M Mansbach, Pamela N Luna, Chad A Shaw, et al.
Journal of Pediatric Genetics|April 3, 2024
<i>FOXP1</i> Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic HerniaKatherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu, et al.
Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2012
Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?Weimin Bi, Caroline Borgan, Amber N Pursley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2012
Incidental copy-number variants identified by routine genome testing in a clinical populationPhilip M Boone, Zachry T Soens, Ian M Campbell, et al.
European Journal of Medical Genetics|July 9, 2013
Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamusYasunari Sakai, Kazuhiro Ohkubo, Yuki Matsushita, et al.
Journal of Molecular and Cellular Cardiology|October 26, 2007
Rapid attenuation of circadian clock gene oscillations in the rat heart following ischemia-reperfusionTheodore A Kung, Oluwaseun Egbejimi, Jiajia Cui, et al.
Microbiome|January 5, 2018
The association between anterior nares and nasopharyngeal microbiota in infants hospitalized for bronchiolitisPamela N Luna, Kohei Hasegawa, Nadim J Ajami, et al.
Investigative Ophthalmology & Visual Science|March 19, 2024
High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and ColobomaBhavana Kunisetty, Bailey A Martin-Giacalone, Xiaonan Zhao, et al.
Genome Medicine|February 4, 2016
A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnosticsRegis A James, Ian M Campbell, Edward S Chen, et al.
Pageof 18

Showing results (71-80 of 172) with videos related to

Sort By:
Pageof 18
The Journal of Allergy and Clinical Immunology|November 19, 2019
Increased Moraxella and Streptococcus species abundance after severe bronchiolitis is associated with recurrent wheezingJonathan M Mansbach, Pamela N Luna, Chad A Shaw, et al.
Journal of Pediatric Genetics|April 3, 2024
<i>FOXP1</i> Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic HerniaKatherine E Pendleton, Andres Hernandez-Garcia, Jennifer M Lyu, et al.
Prenatal Diagnosis|April 4, 2012
Detection of ≥1Mb microdeletions and microduplications in a single cell using custom oligonucleotide arraysWeimin Bi, Amy Breman, Chad A Shaw, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2012
Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today's genomic array era?Weimin Bi, Caroline Borgan, Amber N Pursley, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 11, 2012
Incidental copy-number variants identified by routine genome testing in a clinical populationPhilip M Boone, Zachry T Soens, Ian M Campbell, et al.
European Journal of Medical Genetics|July 9, 2013
Neuroendocrine phenotypes in a boy with 5q14 deletion syndrome implicate the regulatory roles of myocyte-specific enhancer factor 2C in the postnatal hypothalamusYasunari Sakai, Kazuhiro Ohkubo, Yuki Matsushita, et al.
Journal of Molecular and Cellular Cardiology|October 26, 2007
Rapid attenuation of circadian clock gene oscillations in the rat heart following ischemia-reperfusionTheodore A Kung, Oluwaseun Egbejimi, Jiajia Cui, et al.
Microbiome|January 5, 2018
The association between anterior nares and nasopharyngeal microbiota in infants hospitalized for bronchiolitisPamela N Luna, Kohei Hasegawa, Nadim J Ajami, et al.
Investigative Ophthalmology & Visual Science|March 19, 2024
High Clinical Exome Sequencing Diagnostic Rates and Novel Phenotypic Expansions for Nonisolated Microphthalmia, Anophthalmia, and ColobomaBhavana Kunisetty, Bailey A Martin-Giacalone, Xiaonan Zhao, et al.
Genome Medicine|February 4, 2016
A visual and curatorial approach to clinical variant prioritization and disease gene discovery in genome-wide diagnosticsRegis A James, Ian M Campbell, Edward S Chen, et al.
Pageof 18