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Michael L Cunningham

Showing results (141-150 of 162) with videos related to

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American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Genome Biology|June 24, 2008
Gene expression response in target organ and whole blood varies as a function of target organ injury phenotypeEdward K Lobenhofer, J Todd Auman, Pamela E Blackshear, et al.
Plos Genetics|September 21, 2011
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E L M Vissers, Timothy C Cox, A Murat Maga, et al.
Developmental Biology|April 5, 2011
The FaceBase Consortium: a comprehensive program to facilitate craniofacial researchHarry Hochheiser, Bruce J Aronow, Kristin Artinger, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|July 13, 2021
Accuracy and Reliability of 4D-CT and Flexible Laryngoscopy in Upper Airway Evaluation in Robin SequenceAustin S Lam, Michael D Bindschadler, Kelly N Evans, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|September 10, 2005
Chemical effects in biological systems--data dictionary (CEBS-DD): a compendium of terms for the capture and integration of biological study design description, conventional phenotypes, and 'omics dataJennifer Fostel, Danielle Choi, Craig Zwickl, et al.
Plos Genetics|August 26, 2016
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial MorphologyJohn R Shaffer, Ekaterina Orlova, Myoung Keun Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2020
Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020
SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2022
Damaging variants in FOXI3 cause microtia and craniofacial microsomiaDaniel Quiat, Andrew T Timberlake, Justin J Curran, et al.
Pageof 17

Showing results (141-150 of 162) with videos related to

Sort By:
Pageof 17
American Journal of Human Genetics|May 8, 2012
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndromeMark J Rieder, Glenn E Green, Sarah S Park, et al.
Genome Biology|June 24, 2008
Gene expression response in target organ and whole blood varies as a function of target organ injury phenotypeEdward K Lobenhofer, J Todd Auman, Pamela E Blackshear, et al.
Plos Genetics|September 21, 2011
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and miceLisenka E L M Vissers, Timothy C Cox, A Murat Maga, et al.
Developmental Biology|April 5, 2011
The FaceBase Consortium: a comprehensive program to facilitate craniofacial researchHarry Hochheiser, Bruce J Aronow, Kristin Artinger, et al.
Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|July 13, 2021
Accuracy and Reliability of 4D-CT and Flexible Laryngoscopy in Upper Airway Evaluation in Robin SequenceAustin S Lam, Michael D Bindschadler, Kelly N Evans, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology|September 10, 2005
Chemical effects in biological systems--data dictionary (CEBS-DD): a compendium of terms for the capture and integration of biological study design description, conventional phenotypes, and 'omics dataJennifer Fostel, Danielle Choi, Craig Zwickl, et al.
Plos Genetics|August 26, 2016
Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial MorphologyJohn R Shaffer, Ekaterina Orlova, Myoung Keun Lee, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 9, 2020
Correction: SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2020
SMAD6 variants in craniosynostosis: genotype and phenotype evaluationEduardo Calpena, Araceli Cuellar, Krithi Bala, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2022
Damaging variants in FOXI3 cause microtia and craniofacial microsomiaDaniel Quiat, Andrew T Timberlake, Justin J Curran, et al.
Pageof 17