Joris Veltman
0000-0002-3218-8250
Newcastle University
5 papers found
Refreshing results…
Improved phenotypic classification of male infertility to promote discovery of genetic causes
Missense variants in NOX1 and p22phox in a case of very-early-onset inflammatory bowel disease are functionally linked to NOD2
A systematic review and standardized clinical validity assessment of male infertility genes
Validation and application of a novel integrated genetic screening method to a cohort of 1,112 men with idiopathic azoospermia or severe oligozoospermia
Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders
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