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Koenraad Devriendt

Showing results (101-110 of 190) with videos related to

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Plos One|December 16, 2022
Clinical and laboratory characterization of adult sickle cell anemia patients in KinshasaPaul Kabuyi Lumbala, Gloire Mbayabo, Mamy Nzita Ngole, et al.
Journal of Clinical Laboratory Analysis|March 24, 2017
Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemiaTite Minga Mikobi, Prosper Tshilobo Lukusa, Michel Ntetani Aloni, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2014
Switch in FGFR3 and -4 expression profile during human renal development may account for transient hypercalcemia in patients with Sotos syndrome due to 5q35 microdeletionsHenricus A M Mutsaers, Elena N Levtchenko, Laetitia Martinerie, et al.
Plos One|September 30, 2017
Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney diseaseStéphanie De Rechter, Jonathan Kringen, Peter Janssens, et al.
BMJ Open|March 28, 2024
Evaluating offspring Genomic and Epigenomic alterations after prenatal exposure to Cancer treatment In Pregnancy (GE-CIP): a multicentric observational studyIlana Struys, Carolina Velázquez, Koenraad Devriendt, et al.
Clinical Dysmorphology|April 19, 2016
Microtia in Cornelia de Lange syndrome: a case from Democratic Republic of the CongoTony Kayembe Kitenge, Toni Kasole Lubala, Sebastien Mbuyi-Musanzayi, et al.
The Journal of Pediatrics|February 9, 2010
Array comparative genomic hybridization as a diagnostic tool for syndromic heart defectsJeroen Breckpot, Bernard Thienpont, Hilde Peeters, et al.
Journal of Pediatric Genetics|August 11, 2017
Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central AfricaSébastien Mbuyi-Musanzayi, Aimé Lumaka, Toni Lubala Kasole, et al.
Genome Research|July 22, 2025
Genotype imputation from low-coverage data for medical and population genetic analysesSimone Andrea Biagini, Sara Becelaere, Mio Aerden, et al.
Plos Genetics|January 23, 2018
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblingsJacoba J Louw, Ricardo Nunes Bastos, Xiaowen Chen, et al.
Pageof 19

Showing results (101-110 of 190) with videos related to

Sort By:
Pageof 19
Plos One|December 16, 2022
Clinical and laboratory characterization of adult sickle cell anemia patients in KinshasaPaul Kabuyi Lumbala, Gloire Mbayabo, Mamy Nzita Ngole, et al.
Journal of Clinical Laboratory Analysis|March 24, 2017
Protective BCL11A and HBS1L-MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemiaTite Minga Mikobi, Prosper Tshilobo Lukusa, Michel Ntetani Aloni, et al.
The Journal of Clinical Endocrinology and Metabolism|March 28, 2014
Switch in FGFR3 and -4 expression profile during human renal development may account for transient hypercalcemia in patients with Sotos syndrome due to 5q35 microdeletionsHenricus A M Mutsaers, Elena N Levtchenko, Laetitia Martinerie, et al.
Plos One|September 30, 2017
Clinicians' attitude towards family planning and timing of diagnosis in autosomal dominant polycystic kidney diseaseStéphanie De Rechter, Jonathan Kringen, Peter Janssens, et al.
BMJ Open|March 28, 2024
Evaluating offspring Genomic and Epigenomic alterations after prenatal exposure to Cancer treatment In Pregnancy (GE-CIP): a multicentric observational studyIlana Struys, Carolina Velázquez, Koenraad Devriendt, et al.
Clinical Dysmorphology|April 19, 2016
Microtia in Cornelia de Lange syndrome: a case from Democratic Republic of the CongoTony Kayembe Kitenge, Toni Kasole Lubala, Sebastien Mbuyi-Musanzayi, et al.
The Journal of Pediatrics|February 9, 2010
Array comparative genomic hybridization as a diagnostic tool for syndromic heart defectsJeroen Breckpot, Bernard Thienpont, Hilde Peeters, et al.
Journal of Pediatric Genetics|August 11, 2017
Wolf-Hirschhorn Syndrome: Clinical and Genetic Data from a First Case Diagnosed in Central AfricaSébastien Mbuyi-Musanzayi, Aimé Lumaka, Toni Lubala Kasole, et al.
Genome Research|July 22, 2025
Genotype imputation from low-coverage data for medical and population genetic analysesSimone Andrea Biagini, Sara Becelaere, Mio Aerden, et al.
Plos Genetics|January 23, 2018
Compound heterozygous loss-of-function mutations in KIF20A are associated with a novel lethal congenital cardiomyopathy in two siblingsJacoba J Louw, Ricardo Nunes Bastos, Xiaowen Chen, et al.
Pageof 19