Search research articles
Contact Us
Filters
Showing results (21-30 of 73) with videos related to
Page
of 8
Sort By:
American Journal of Medical Genetics. Part A
|
August 3, 2016
3D morphometry aids facial analysis of individuals with a childhood cancer
Saskia M J Hopman, Johannes H M Merks, Michael Suttie, et al.
European Journal of Human Genetics : EJHG
|
January 9, 2014
Face shape differs in phylogenetically related populations
Saskia M J Hopman, Johannes H M Merks, Michael Suttie, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
October 11, 2016
Combined soft and skeletal tissue modelling of normal and dysmorphic midface postnatal development
Amel Ibrahim, Michael Suttie, Neil W Bulstrode, et al.
European Journal of Human Genetics : EJHG
|
March 1, 2007
Three-dimensional face shape in Fabry disease
Josanne Cox-Brinkman, Anouk Vedder, Carla Hollak, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2013
Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome
Erica F Andersen, John C Carey, Dawn L Earl, et al.
Physical Review Letters
|
June 10, 2024
Neutrino Trapping and Out-of-Equilibrium Effects in Binary Neutron-Star Merger Remnants
Pedro Luis Espino, Peter Hammond, David Radice, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2013
Growth hormone, gender and face shape in Prader-Willi syndrome
Mauren Abreu de Souza, Catherine McAllister, Michael Suttie, et al.
The Journal of Craniofacial Surgery
|
October 16, 2018
Objectifying Micrognathia Using Three-Dimensional Photogrammetric Analysis
Hanneke Basart, Michael Suttie, Amel Ibrahim, et al.
Human Molecular Genetics
|
August 4, 2009
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes
Erwin Pauws, Aya Hoshino, Lucy Bentley, et al.
Research in Developmental Disabilities
|
September 4, 2012
Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology
Brooke Sinderberry, Scott Brown, Peter Hammond, et al.
Page
of 8
Search research articles
Search
Showing results (21-30 of 73) with videos related to
Sort By:
Page
of 8
American Journal of Medical Genetics. Part A
|
August 3, 2016
3D morphometry aids facial analysis of individuals with a childhood cancer
Saskia M J Hopman, Johannes H M Merks, Michael Suttie, et al.
European Journal of Human Genetics : EJHG
|
January 9, 2014
Face shape differs in phylogenetically related populations
Saskia M J Hopman, Johannes H M Merks, Michael Suttie, et al.
Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery
|
October 11, 2016
Combined soft and skeletal tissue modelling of normal and dysmorphic midface postnatal development
Amel Ibrahim, Michael Suttie, Neil W Bulstrode, et al.
European Journal of Human Genetics : EJHG
|
March 1, 2007
Three-dimensional face shape in Fabry disease
Josanne Cox-Brinkman, Anouk Vedder, Carla Hollak, et al.
European Journal of Human Genetics : EJHG
|
August 22, 2013
Deletions involving genes WHSC1 and LETM1 may be necessary, but are not sufficient to cause Wolf-Hirschhorn Syndrome
Erica F Andersen, John C Carey, Dawn L Earl, et al.
Physical Review Letters
|
June 10, 2024
Neutrino Trapping and Out-of-Equilibrium Effects in Binary Neutron-Star Merger Remnants
Pedro Luis Espino, Peter Hammond, David Radice, et al.
American Journal of Medical Genetics. Part A
|
August 7, 2013
Growth hormone, gender and face shape in Prader-Willi syndrome
Mauren Abreu de Souza, Catherine McAllister, Michael Suttie, et al.
The Journal of Craniofacial Surgery
|
October 16, 2018
Objectifying Micrognathia Using Three-Dimensional Photogrammetric Analysis
Hanneke Basart, Michael Suttie, Amel Ibrahim, et al.
Human Molecular Genetics
|
August 4, 2009
Tbx22null mice have a submucous cleft palate due to reduced palatal bone formation and also display ankyloglossia and choanal atresia phenotypes
Erwin Pauws, Aya Hoshino, Lucy Bentley, et al.
Research in Developmental Disabilities
|
September 4, 2012
Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology
Brooke Sinderberry, Scott Brown, Peter Hammond, et al.
Page
of 8