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Frontiers in Digital Health
|
April 23, 2026
Advancing the adoption of oncology decision support tools in Europe: insights from CAN.HEAL
Nancy Frederickx, Guy Froyen, Maud Kamal, et al.
Nature Communications
|
March 26, 2021
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities
Bénedith Oben, Guy Froyen, Kylee H Maclachlan, et al.
American Journal of Human Genetics
|
July 31, 2012
Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements
Guy Froyen, Stefanie Belet, Francisco Martinez, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
Nature Communications
|
September 10, 2014
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
Shai Carmi, Ken Y Hui, Ethan Kochav, et al.
NPJ Precision Oncology
|
March 11, 2025
A nationwide comprehensive genomic profiling and molecular tumor board platform for patients with advanced cancer
Pieter-Jan Volders, Philippe Aftimos, Franceska Dedeurwaerdere, et al.
Human Genetics
|
December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome
R S Møller, L R Jensen, S M Maas, et al.
American Journal of Human Genetics
|
February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation
Guy Froyen, Mark Corbett, Joke Vandewalle, et al.
American Journal of Medical Genetics. Part A
|
February 27, 2010
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation
Dorien Lugtenberg, Luiz Zangrande-Vieira, Maria Kirchhoff, et al.
Human Mutation
|
January 16, 2007
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium
Arjan P M de Brouwer, Helger G Yntema, Tjitske Kleefstra, et al.
Page
of 18
Search research articles
Search
Showing results (161-170 of 172) with videos related to
Sort By:
Page
of 18
Frontiers in Digital Health
|
April 23, 2026
Advancing the adoption of oncology decision support tools in Europe: insights from CAN.HEAL
Nancy Frederickx, Guy Froyen, Maud Kamal, et al.
Nature Communications
|
March 26, 2021
Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities
Bénedith Oben, Guy Froyen, Kylee H Maclachlan, et al.
American Journal of Human Genetics
|
July 31, 2012
Copy-number gains of HUWE1 due to replication- and recombination-based rearrangements
Guy Froyen, Stefanie Belet, Francisco Martinez, et al.
European Journal of Human Genetics : EJHG
|
April 10, 2008
MCT8 mutation analysis and identification of the first female with Allan-Herndon-Dudley syndrome due to loss of MCT8 expression
Suzanna Gerarda Maria Frints, Steffen Lenzner, Mareike Bauters, et al.
Nature Communications
|
September 10, 2014
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
Shai Carmi, Ken Y Hui, Ethan Kochav, et al.
NPJ Precision Oncology
|
March 11, 2025
A nationwide comprehensive genomic profiling and molecular tumor board platform for patients with advanced cancer
Pieter-Jan Volders, Philippe Aftimos, Franceska Dedeurwaerdere, et al.
Human Genetics
|
December 12, 2013
X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome
R S Møller, L R Jensen, S M Maas, et al.
American Journal of Human Genetics
|
February 7, 2008
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation
Guy Froyen, Mark Corbett, Joke Vandewalle, et al.
American Journal of Medical Genetics. Part A
|
February 27, 2010
Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation
Dorien Lugtenberg, Luiz Zangrande-Vieira, Maria Kirchhoff, et al.
Human Mutation
|
January 16, 2007
Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium
Arjan P M de Brouwer, Helger G Yntema, Tjitske Kleefstra, et al.
Page
of 18