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Geert Mortier

Showing results (91-100 of 156) with videos related to

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Vaccine|March 14, 2020
Transcriptomic profiling of different responder types in adults after a Priorix® vaccinationEsther Bartholomeus, Nicolas De Neuter, Arvid Suls, et al.
Genes and Immunity|June 16, 2018
Memory CD4<sup>+</sup> T cell receptor repertoire data mining as a tool for identifying cytomegalovirus serostatusNicolas De Neuter, Esther Bartholomeus, George Elias, et al.
Orphanet Journal of Rare Diseases|July 27, 2022
Optimising the diagnosis and referral of achondroplasia in Europe: European Achondroplasia Forum best practice recommendationsValerie Cormier-Daire, Moeenaldeen AlSayed, Inês Alves, et al.
European Journal of Medical Genetics|March 21, 2009
The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human heightKaren Buysse, William Reardon, Lakshmi Mehta, et al.
Journal of the Endocrine Society|March 2, 2022
Broadening the Spectrum of Loss-of-Function Variants in NPR-C-Related Extreme Tall StaturePeter Lauffer, Eveline Boudin, Daniëlle C M van der Kaay, et al.
BMC Bioinformatics|May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarraysBjörn Menten, Filip Pattyn, Katleen De Preter, et al.
Orphanet Journal of Rare Diseases|August 20, 2022
Optimising care and follow-up of adults with achondroplasiaSvein Fredwall, Yana Allum, Moeenaldeen AlSayed, et al.
Journal of Medical Genetics|April 9, 2016
Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneityAritoshi Iida, Weirong Xing, Martine K F Docx, et al.
Journal of Medical Genetics|July 2, 2013
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactylyNicolas Simonis, Isabelle Migeotte, Nelle Lambert, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1Diana Mitter, Barbara Delle Chiaie, Hermann-Josef Lüdecke, et al.
Pageof 16

Showing results (91-100 of 156) with videos related to

Sort By:
Pageof 16
Vaccine|March 14, 2020
Transcriptomic profiling of different responder types in adults after a Priorix® vaccinationEsther Bartholomeus, Nicolas De Neuter, Arvid Suls, et al.
Genes and Immunity|June 16, 2018
Memory CD4<sup>+</sup> T cell receptor repertoire data mining as a tool for identifying cytomegalovirus serostatusNicolas De Neuter, Esther Bartholomeus, George Elias, et al.
Orphanet Journal of Rare Diseases|July 27, 2022
Optimising the diagnosis and referral of achondroplasia in Europe: European Achondroplasia Forum best practice recommendationsValerie Cormier-Daire, Moeenaldeen AlSayed, Inês Alves, et al.
European Journal of Medical Genetics|March 21, 2009
The 12q14 microdeletion syndrome: additional patients and further evidence that HMGA2 is an important genetic determinant for human heightKaren Buysse, William Reardon, Lakshmi Mehta, et al.
Journal of the Endocrine Society|March 2, 2022
Broadening the Spectrum of Loss-of-Function Variants in NPR-C-Related Extreme Tall StaturePeter Lauffer, Eveline Boudin, Daniëlle C M van der Kaay, et al.
BMC Bioinformatics|May 25, 2005
arrayCGHbase: an analysis platform for comparative genomic hybridization microarraysBjörn Menten, Filip Pattyn, Katleen De Preter, et al.
Orphanet Journal of Rare Diseases|August 20, 2022
Optimising care and follow-up of adults with achondroplasiaSvein Fredwall, Yana Allum, Moeenaldeen AlSayed, et al.
Journal of Medical Genetics|April 9, 2016
Identification of biallelic LRRK1 mutations in osteosclerotic metaphyseal dysplasia and evidence for locus heterogeneityAritoshi Iida, Weirong Xing, Martine K F Docx, et al.
Journal of Medical Genetics|July 2, 2013
FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactylyNicolas Simonis, Isabelle Migeotte, Nelle Lambert, et al.
American Journal of Medical Genetics. Part A|April 29, 2010
Genotype-phenotype correlation in eight new patients with a deletion encompassing 2q31.1Diana Mitter, Barbara Delle Chiaie, Hermann-Josef Lüdecke, et al.
Pageof 16