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Geert Mortier

Showing results (21-30 of 156) with videos related to

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Journal of Fluency Disorders|April 24, 2010
Speech fluency in neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
Journal of Communication Disorders|December 24, 2011
Articulation in schoolchildren and adults with neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
Seminars in Arthritis and Rheumatism|April 1, 2014
Mutation in the type II collagen gene (COL2AI) as a cause of primary osteoarthritis associated with mild spondyloepiphyseal involvementIva Rukavina, Geert Mortier, Lut Van Laer, et al.
Calcified Tissue International|November 25, 2019
WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in OsteoblastsGretl Hendrickx, Eveline Boudin, Marinus Verbeek, et al.
Clinical Genetics|December 18, 2023
RUNX2-related metaphyseal dysplasia with maxillary hypoplasia: A rare skeletal disorder resembling SFRP4-related Pyle diseaseEwa Hordyjewska-Kowalczyk, Wim Wuyts, Nele Boeckx, et al.
Human Mutation|June 29, 2004
X-linked spondyloepiphyseal dysplasia tarda: Novel and recurrent mutations in 13 European familiesJörg Fiedler, Martine Le Merrer, Geert Mortier, et al.
Bone|April 9, 2013
No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disordersEveline Boudin, Karen Jennes, Fenna de Freitas, et al.
International Journal of Pediatric Otorhinolaryngology|December 15, 2010
Overall intelligibility, articulation, resonance, voice and language in a child with Nager syndromeKristiane M Van Lierde, Anke Luyten, Geert Mortier, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|May 3, 2016
Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfectaLucie Hruskova, Igor Fijalkowski, Wim Van Hul, et al.
Journal of Pediatric Genetics|September 15, 2016
A STAT3 mutation in hyper-immunoglobulin E syndrome: A case reportFilip Haenen, Marielle Alders, Elke Dierckx, et al.
Pageof 16

Showing results (21-30 of 156) with videos related to

Sort By:
Pageof 16
Journal of Fluency Disorders|April 24, 2010
Speech fluency in neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
Journal of Communication Disorders|December 24, 2011
Articulation in schoolchildren and adults with neurofibromatosis type 1Marjan Cosyns, Geert Mortier, Sandra Janssens, et al.
Seminars in Arthritis and Rheumatism|April 1, 2014
Mutation in the type II collagen gene (COL2AI) as a cause of primary osteoarthritis associated with mild spondyloepiphyseal involvementIva Rukavina, Geert Mortier, Lut Van Laer, et al.
Calcified Tissue International|November 25, 2019
WNT16 Requires Gα Subunits as Intracellular Partners for Both Its Canonical and Non-Canonical WNT Signalling Activity in OsteoblastsGretl Hendrickx, Eveline Boudin, Marinus Verbeek, et al.
Clinical Genetics|December 18, 2023
RUNX2-related metaphyseal dysplasia with maxillary hypoplasia: A rare skeletal disorder resembling SFRP4-related Pyle diseaseEwa Hordyjewska-Kowalczyk, Wim Wuyts, Nele Boeckx, et al.
Human Mutation|June 29, 2004
X-linked spondyloepiphyseal dysplasia tarda: Novel and recurrent mutations in 13 European familiesJörg Fiedler, Martine Le Merrer, Geert Mortier, et al.
Bone|April 9, 2013
No mutations in the serotonin related TPH1 and HTR1B genes in patients with monogenic sclerosing bone disordersEveline Boudin, Karen Jennes, Fenna de Freitas, et al.
International Journal of Pediatric Otorhinolaryngology|December 15, 2010
Overall intelligibility, articulation, resonance, voice and language in a child with Nager syndromeKristiane M Van Lierde, Anke Luyten, Geert Mortier, et al.
Biomedical Papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia|May 3, 2016
Eight mutations including 5 novel ones in the COL1A1 gene in Czech patients with osteogenesis imperfectaLucie Hruskova, Igor Fijalkowski, Wim Van Hul, et al.
Journal of Pediatric Genetics|September 15, 2016
A STAT3 mutation in hyper-immunoglobulin E syndrome: A case reportFilip Haenen, Marielle Alders, Elke Dierckx, et al.
Pageof 16