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European Journal of Medical Genetics|July 26, 2011
Limb skeletal malformations - what the HOX is going on?Nathalie Brison, Przemko Tylzanowski, Philippe Debeer
Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 17, 2013
Joining the fingers: a HOXD13 StoryNathalie Brison, Philippe Debeer, Przemko Tylzanowski
American Journal of Medical Genetics. Part A|October 15, 2013
Genetic counseling for susceptibility loci and neurodevelopmental disorders: the del15q11.2 as an exampleVeerle De Wolf, Nathalie Brison, Koenraad Devriendt, et al.
Statistical Applications in Genetics and Molecular Biology|May 1, 2018
Noise-robust assessment of SNP array based CNV calls through local noise estimation of log R ratiosNele Cosemans, Peter Claes, Nathalie Brison, et al.
Human Molecular Genetics|December 9, 2008
A G220V substitution within the N-terminal transcription regulating domain of HOXD13 causes a variant synpolydactyly phenotypeSebastian Fantini, Giulia Vaccari, Nathalie Brison, et al.
European Journal of Human Genetics : EJHG|January 10, 2024
Expanding the phenotype of copy number variations involving NR0B1 (DAX1)Nathalie Veyt, Griet Van Buggenhout, Koen Devriendt, et al.
Human Molecular Genetics|March 1, 2012
An N-terminal G11A mutation in HOXD13 causes synpolydactyly and interferes with Gli3R function during limb pre-patterningNathalie Brison, Philippe Debeer, Sebastian Fantini, et al.
Prenatal Diagnosis|December 15, 2017
Maternal liver transplant: Another cause of discordant fetal sex determination using cell-free DNAMaria Neofytou, Nathalie Brison, Kris Van den Bogaert, et al.
Prenatal Diagnosis|August 18, 2021
Non-invasive prenatal testing suggesting a maternal malignancy: What do we tell the prospective parents in Belgium?Lore Lannoo, Liesbeth Lenaerts, Kris Van Den Bogaert, et al.
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