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Malawi Medical Journal : the Journal of Medical Association of Malawi
|
November 30, 2016
Four artemisinin-based treatments in African pregnant women with malaria
, Divine Pekyi, Akua A Ampromfi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 10, 2021
Outcome of publicly funded nationwide first-tier noninvasive prenatal screening
Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, et al.
Annals of Palliative Medicine
|
June 12, 2023
A critical appraisal of the four systematic reviews and meta-analysis on stereotactic body radiation therapy versus external beam radiotherapy for painful bone metastases and where we go from here
Henry C Y Wong, Adrian Wai Chan, Peter Johnstone, et al.
Prenatal Diagnosis
|
October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Cell Reports
|
December 16, 2014
Genomic and functional overlap between somatic and germline chromosomal rearrangements
Sebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, et al.
European Journal of Human Genetics : EJHG
|
March 12, 2015
Redefining the MED13L syndrome
Abidemi Adegbola, Luciana Musante, Bert Callewaert, et al.
American Journal of Human Genetics
|
May 14, 2025
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder
María Del Rocío Pérez Baca, María Palomares-Bralo, Michiel Vanhooydonck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity
Nina De Rocker, Sarah Vergult, David Koolen, et al.
European Journal of Medical Genetics
|
March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals
E K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.
European Journal of Medical Genetics
|
February 19, 2014
Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges
Olivier Vanakker, Catheline Vilain, Katrien Janssens, et al.
Page
of 58
Search research articles
Search
Showing results (541-550 of 571) with videos related to
Sort By:
Page
of 58
Malawi Medical Journal : the Journal of Medical Association of Malawi
|
November 30, 2016
Four artemisinin-based treatments in African pregnant women with malaria
, Divine Pekyi, Akua A Ampromfi, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 10, 2021
Outcome of publicly funded nationwide first-tier noninvasive prenatal screening
Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, et al.
Annals of Palliative Medicine
|
June 12, 2023
A critical appraisal of the four systematic reviews and meta-analysis on stereotactic body radiation therapy versus external beam radiotherapy for painful bone metastases and where we go from here
Henry C Y Wong, Adrian Wai Chan, Peter Johnstone, et al.
Prenatal Diagnosis
|
October 19, 2018
The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, et al.
Cell Reports
|
December 16, 2014
Genomic and functional overlap between somatic and germline chromosomal rearrangements
Sebastiaan van Heesch, Marieke Simonis, Markus J van Roosmalen, et al.
European Journal of Human Genetics : EJHG
|
March 12, 2015
Redefining the MED13L syndrome
Abidemi Adegbola, Luciana Musante, Bert Callewaert, et al.
American Journal of Human Genetics
|
May 14, 2025
Loss of function of the zinc finger homeobox 4 gene, ZFHX4, underlies a neurodevelopmental disorder
María Del Rocío Pérez Baca, María Palomares-Bralo, Michiel Vanhooydonck, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesity
Nina De Rocker, Sarah Vergult, David Koolen, et al.
European Journal of Medical Genetics
|
March 25, 2009
Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals
E K Bijlsma, A C J Gijsbers, J H M Schuurs-Hoeijmakers, et al.
European Journal of Medical Genetics
|
February 19, 2014
Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges
Olivier Vanakker, Catheline Vilain, Katrien Janssens, et al.
Page
of 58