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Trends in Molecular Medicine
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June 9, 2020
Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular Intersection
Aline Verstraeten, Josephina Meester, Silke Peeters, et al.
Journal of Fluency Disorders
|
September 14, 2010
Word-final prolongations in an adult male with neurofibromatosis type 1
Marjan Cosyns, Geert Mortier, Paul Corthals, et al.
Journal of Voice : Official Journal of the Voice Foundation
|
October 19, 2010
Voice characteristics in adults with neurofibromatosis type 1
Marjan Cosyns, Geert Mortier, Paul Corthals, et al.
American Journal of Human Genetics
|
August 19, 2007
Type and level of RMRP functional impairment predicts phenotype in the cartilage hair hypoplasia-anauxetic dysplasia spectrum
Christian T Thiel, Geert Mortier, Ilkka Kaitila, et al.
American Journal of Medical Genetics. Part A
|
November 5, 2011
Objective assessment of nasality in Flemish adults with neurofibromatosis type 1
Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
International Journal of Language & Communication Disorders
|
November 11, 2009
Speech disorders in neurofibromatosis type 1: a sample survey
Marjan Cosyns, Lies Vandeweghe, Geert Mortier, et al.
Genome Biology
|
February 13, 2007
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
Jan Hellemans, Geert Mortier, Anne De Paepe, et al.
European Journal of Pediatrics
|
May 19, 2011
Tetrasomy and pentasomy of the X chromosome
Edith Schoubben, Karin Decaestecker, Koen Quaegebeur, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2012
Spondyloperipheral dysplasia as the mosaic form of platyspondylic lethal skeletal dyplasia torrance type in mother and fetus with the same COL2A1 mutation
Julie Désir, Marie Cassart, Catherine Donner, et al.
Calcified Tissue International
|
October 29, 2009
The heterozygous Lemd3 +/GT mouse is not a murine model for osteopoikilosis in humans
Annelies Dheedene, Steven Deleye, Jan Hellemans, et al.
Page
of 16
Search research articles
Search
Showing results (11-20 of 156) with videos related to
Sort By:
Page
of 16
Trends in Molecular Medicine
|
June 9, 2020
Chondrodysplasias and Aneurysmal Thoracic Aortopathy: An Emerging Tale of Molecular Intersection
Aline Verstraeten, Josephina Meester, Silke Peeters, et al.
Journal of Fluency Disorders
|
September 14, 2010
Word-final prolongations in an adult male with neurofibromatosis type 1
Marjan Cosyns, Geert Mortier, Paul Corthals, et al.
Journal of Voice : Official Journal of the Voice Foundation
|
October 19, 2010
Voice characteristics in adults with neurofibromatosis type 1
Marjan Cosyns, Geert Mortier, Paul Corthals, et al.
American Journal of Human Genetics
|
August 19, 2007
Type and level of RMRP functional impairment predicts phenotype in the cartilage hair hypoplasia-anauxetic dysplasia spectrum
Christian T Thiel, Geert Mortier, Ilkka Kaitila, et al.
American Journal of Medical Genetics. Part A
|
November 5, 2011
Objective assessment of nasality in Flemish adults with neurofibromatosis type 1
Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
International Journal of Language & Communication Disorders
|
November 11, 2009
Speech disorders in neurofibromatosis type 1: a sample survey
Marjan Cosyns, Lies Vandeweghe, Geert Mortier, et al.
Genome Biology
|
February 13, 2007
qBase relative quantification framework and software for management and automated analysis of real-time quantitative PCR data
Jan Hellemans, Geert Mortier, Anne De Paepe, et al.
European Journal of Pediatrics
|
May 19, 2011
Tetrasomy and pentasomy of the X chromosome
Edith Schoubben, Karin Decaestecker, Koen Quaegebeur, et al.
American Journal of Medical Genetics. Part A
|
April 13, 2012
Spondyloperipheral dysplasia as the mosaic form of platyspondylic lethal skeletal dyplasia torrance type in mother and fetus with the same COL2A1 mutation
Julie Désir, Marie Cassart, Catherine Donner, et al.
Calcified Tissue International
|
October 29, 2009
The heterozygous Lemd3 +/GT mouse is not a murine model for osteopoikilosis in humans
Annelies Dheedene, Steven Deleye, Jan Hellemans, et al.
Page
of 16