Publications by authors named "Crool Velter"

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Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice.
Suzanne C E H Sallevelt, Alexander P A Stegmann, Bart de Koning, Crool Velter, Anja Steyls

Genet Med· June 2021

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Rare novel variants in the ZIC3 gene cause X-linked heterotaxy.
Aimee D C Paulussen, Anja Steyls, Jo Vanoevelen, Florence Hj van Tienen, Ingrid P C Krapels, Crool Velter

Eur J Hum Genet· December 2016

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DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.
Roselie Jongbloed, Carlo Marcelis, Crool Velter, Pieter Doevendans, Joep Geraedts

Hum Mutat· November 2002

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