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IEEE Access : Practical Innovations, Open Solutions
|
August 14, 2025
A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder
Soha S Mahdi, Eduarda Caldeira, Harold Matthews, et al.
American Journal of Medical Genetics. Part A
|
April 21, 2004
3D analysis of facial morphology
Peter Hammond, Tim J Hutton, Judith E Allanson, et al.
Journal of Medical Genetics
|
November 20, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2025
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Pediatric Blood & Cancer
|
April 20, 2017
Facial asymmetry in head and neck rhabdomyosarcoma survivors
Reineke A Schoot, Marinka L F Hol, Johannes H M Merks, et al.
Scientific Reports
|
June 10, 2021
Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism
Harold S Matthews, Richard L Palmer, Gareth S Baynam, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome
Jonathan L Tobin, Matt Di Franco, Erica Eichers, et al.
Intensive Care Medicine Experimental
|
February 29, 2024
Development of personalized non-invasive ventilation masks for critically ill children: a bench study
Rosemijne R W P Pigmans, Rozalinde Klein-Blommert, Monica C van Gestel, et al.
Plos One
|
August 23, 2011
Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions
Dalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, et al.
BMJ Open
|
January 23, 2017
Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre study
Floor A M Postema, Saskia M J Hopman, Corianne A J M de Borgie, et al.
Page
of 8
Search research articles
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Showing results (51-60 of 73) with videos related to
Sort By:
Page
of 8
IEEE Access : Practical Innovations, Open Solutions
|
August 14, 2025
A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder
Soha S Mahdi, Eduarda Caldeira, Harold Matthews, et al.
American Journal of Medical Genetics. Part A
|
April 21, 2004
3D analysis of facial morphology
Peter Hammond, Tim J Hutton, Judith E Allanson, et al.
Journal of Medical Genetics
|
November 20, 2025
Advancing genotype-phenotype analysis through 3D facial morphometry: insights from Cri-du-Chat syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Medrxiv : the Preprint Server for Health Sciences
|
June 10, 2025
Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome
Michiel Vanneste, Harold Matthews, Yoeri Sleyp, et al.
Pediatric Blood & Cancer
|
April 20, 2017
Facial asymmetry in head and neck rhabdomyosarcoma survivors
Reineke A Schoot, Marinka L F Hol, Johannes H M Merks, et al.
Scientific Reports
|
June 10, 2021
Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism
Harold S Matthews, Richard L Palmer, Gareth S Baynam, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 30, 2008
Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome
Jonathan L Tobin, Matt Di Franco, Erica Eichers, et al.
Intensive Care Medicine Experimental
|
February 29, 2024
Development of personalized non-invasive ventilation masks for critically ill children: a bench study
Rosemijne R W P Pigmans, Rozalinde Klein-Blommert, Monica C van Gestel, et al.
Plos One
|
August 23, 2011
Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletions
Dalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, et al.
BMJ Open
|
January 23, 2017
Validation of a clinical screening instrument for tumour predisposition syndromes in patients with childhood cancer (TuPS): protocol for a prospective, observational, multicentre study
Floor A M Postema, Saskia M J Hopman, Corianne A J M de Borgie, et al.
Page
of 8