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Laura Vandenhove
Laura Vandenhove
Katholieke Universiteit Leuven
Intellectual disability
Genetics
Biology
Medicine
Breakpoint
4
Papers
11
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The clinical relevance of intragenic NRXN1 deletions
2020
Journal of Medical Genetics
Nele Cosemans
Laura Vandenhove
Annick Vogels
Koenraad Devriendt
Hilde Van Esch
Griet Van Buggenhout
Hilde Olivié
Thomy de Ravel
Els Ortibus
Eric Legius
Peter Aerssens
Jeroen Breckpot
Joris Vermeesch
Sanbing Shen
Jacqueline Fitzgerald
Louise Gallagher
Hilde Peeters
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Citations (3)
ZNF462 and KLF12 are disrupted by a de novo translocation in a patient with syndromic intellectual disability and autism spectrum disorder
2018
European Journal of Medical Genetics
Nele Cosemans
Laura Vandenhove
Jarymke Maljaars
Hilde Van Esch
Koenraad Devriendt
Amanda Baldwin
Jean-Pierre Fryns
Ilse Noens
Hilde Peeters
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Citations (8)
The clinical relevance of intragenic NRXN1 deletions
2017
Nele Cosemans
Laura Vandenhove
Greet Peeters
Thomy de Ravel de lArgentière
Koenraad Devriendt
Eric Legius E
Griet Van Buggenhout
Hilde Van Esch
Annick Vogels A
Joris Vermeesch
Hilde Peeters
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ZNF462 mutations cause syndromic intellectual disability with ptosis and distinct craniofacial anomalies
2017
Nele Cosemans
Laura Vandenhove
Ilse Noens
Jarymke Maljaars
Koenraad Devriendt
Jean-Pierre Fryns
A. Baldwin
Hilde Peeters
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