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Journal of Anatomy
|
June 19, 2012
Sexual dimorphism in multiple aspects of 3D facial symmetry and asymmetry defined by spatially dense geometric morphometrics
Peter Claes, Mark Walters, Mark D Shriver, et al.
Frontiers in Public Health
|
March 14, 2017
Outcomes of an International Workshop on Preconception Expanded Carrier Screening: Some Considerations for Governments
Caron M Molster, Karla Lister, Selina Metternick-Jones, et al.
Frontiers in Public Health
|
December 25, 2025
The United Nations convention on rare diseases-A framework for research prioritization
Mohammed Junaid, Jenny Downs, Tudor Groza, et al.
Stem Cell Research & Therapy
|
February 10, 2022
CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency
Vanessa S Fear, Catherine A Forbes, Denise Anderson, et al.
Developmental Medicine and Child Neurology
|
January 17, 2018
Cerebral palsy and genomics: an international consortium
Alastair H MacLennan, Michael C Kruer, Gareth Baynam, et al.
Database : the Journal of Biological Databases and Curation
|
March 1, 2015
Automatic concept recognition using the human phenotype ontology reference and test suite corpora
Tudor Groza, Sebastian Köhler, Sandra Doelken, et al.
Frontiers in Public Health
|
January 6, 2025
"Equity" in genomic health policies: a review of policies in the international arena
Prabhathi Basnayake Ralalage, Tala Mitchell, Claire Zammit, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 18, 2014
Multinodular Goiter in children: an important pointer to a germline DICER1 mutation
Shoshana R Rath, Anthony Bartley, Adrian Charles, et al.
Clinical Genetics
|
June 1, 2022
Further evidence for distinct traits associated with RBM10 missense variants
Cathryn Poulton, Gareth Baynam, Kye Pugh, et al.
Nature
|
December 13, 2023
Indigenous Australian genomes show deep structure and rich novel variation
Matthew Silcocks, Ashley Farlow, Azure Hermes, et al.
Page
of 18
Search research articles
Search
Showing results (71-80 of 178) with videos related to
Sort By:
Page
of 18
Journal of Anatomy
|
June 19, 2012
Sexual dimorphism in multiple aspects of 3D facial symmetry and asymmetry defined by spatially dense geometric morphometrics
Peter Claes, Mark Walters, Mark D Shriver, et al.
Frontiers in Public Health
|
March 14, 2017
Outcomes of an International Workshop on Preconception Expanded Carrier Screening: Some Considerations for Governments
Caron M Molster, Karla Lister, Selina Metternick-Jones, et al.
Frontiers in Public Health
|
December 25, 2025
The United Nations convention on rare diseases-A framework for research prioritization
Mohammed Junaid, Jenny Downs, Tudor Groza, et al.
Stem Cell Research & Therapy
|
February 10, 2022
CRISPR single base editing, neuronal disease modelling and functional genomics for genetic variant analysis: pipeline validation using Kleefstra syndrome EHMT1 haploinsufficiency
Vanessa S Fear, Catherine A Forbes, Denise Anderson, et al.
Developmental Medicine and Child Neurology
|
January 17, 2018
Cerebral palsy and genomics: an international consortium
Alastair H MacLennan, Michael C Kruer, Gareth Baynam, et al.
Database : the Journal of Biological Databases and Curation
|
March 1, 2015
Automatic concept recognition using the human phenotype ontology reference and test suite corpora
Tudor Groza, Sebastian Köhler, Sandra Doelken, et al.
Frontiers in Public Health
|
January 6, 2025
"Equity" in genomic health policies: a review of policies in the international arena
Prabhathi Basnayake Ralalage, Tala Mitchell, Claire Zammit, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 18, 2014
Multinodular Goiter in children: an important pointer to a germline DICER1 mutation
Shoshana R Rath, Anthony Bartley, Adrian Charles, et al.
Clinical Genetics
|
June 1, 2022
Further evidence for distinct traits associated with RBM10 missense variants
Cathryn Poulton, Gareth Baynam, Kye Pugh, et al.
Nature
|
December 13, 2023
Indigenous Australian genomes show deep structure and rich novel variation
Matthew Silcocks, Ashley Farlow, Azure Hermes, et al.
Page
of 18