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Showing results (51-60 of 61) with videos related to

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Journal of Anatomy|September 24, 2025
Histological analysis of the semitendinosus muscle in young children with cerebral palsy compared to age matched typically developing childrenJorieke M Deschrevel, Anke A Andries, Karen Maes, et al.
Frontiers in Physiology|July 31, 2025
Correction: Histological analysis of the medial gastrocnemius muscle in young healthy childrenAnke Andries, Jorieke Deschrevel, Karen Maes, et al.
Frontiers in Physiology|April 23, 2024
Histological analysis of the medial gastrocnemius muscle in young healthy childrenAnke Andries, Jorieke Deschrevel, Karen Maes, et al.
Plos Genetics|May 13, 2021
3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologiesHanne Hoskens, Dongjing Liu, Sahin Naqvi, et al.
Genes|December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility GeneIris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Nature Genetics|December 8, 2020
Insights into the genetic architecture of the human faceJulie D White, Karlijne Indencleef, Sahin Naqvi, et al.
Frontiers in Genetics|March 11, 2021
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial VariationKarlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disabilityRosalind Verheije, Gabriel S Kupchik, Bertrand Isidor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesisCharlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, et al.
Pageof 7

Showing results (51-60 of 61) with videos related to

Sort By:
Pageof 7
Journal of Anatomy|September 24, 2025
Histological analysis of the semitendinosus muscle in young children with cerebral palsy compared to age matched typically developing childrenJorieke M Deschrevel, Anke A Andries, Karen Maes, et al.
Frontiers in Physiology|July 31, 2025
Correction: Histological analysis of the medial gastrocnemius muscle in young healthy childrenAnke Andries, Jorieke Deschrevel, Karen Maes, et al.
Frontiers in Physiology|April 23, 2024
Histological analysis of the medial gastrocnemius muscle in young healthy childrenAnke Andries, Jorieke Deschrevel, Karen Maes, et al.
Plos Genetics|May 13, 2021
3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologiesHanne Hoskens, Dongjing Liu, Sahin Naqvi, et al.
Genes|December 11, 2019
Non-Syndromic Cleft Lip with or without Cleft Palate: Genome-Wide Association Study in Europeans Identifies a Suggestive Risk Locus at 16p12.1 and Supports <i>SH3PXD2A</i> as a Clefting Susceptibility GeneIris Alm van Rooij, Kerstin U Ludwig, Julia Welzenbach, et al.
Nature Genetics|December 8, 2020
Insights into the genetic architecture of the human faceJulie D White, Karlijne Indencleef, Sahin Naqvi, et al.
Frontiers in Genetics|March 11, 2021
The Intersection of the Genetic Architectures of Orofacial Clefts and Normal Facial VariationKarlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, et al.
European Journal of Human Genetics : EJHG|March 10, 2019
Deletions and loss-of-function variants in TP63 associated with orofacial cleftingKriti D Khandelwal, Marie-José H van den Boogaard, Sarah L Mehrem, et al.
European Journal of Human Genetics : EJHG|October 7, 2018
Heterozygous loss-of-function variants of MEIS2 cause a triad of palatal defects, congenital heart defects, and intellectual disabilityRosalind Verheije, Gabriel S Kupchik, Bertrand Isidor, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2016
Novel mutations in LRP6 highlight the role of WNT signaling in tooth agenesisCharlotte W Ockeloen, Kriti D Khandelwal, Karoline Dreesen, et al.
Pageof 7