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European Journal of Endocrinology|December 3, 2003
Do patients with multiple endocrine neoplasia syndrome type 1 benefit from periodical screening?Engelien A M Geerdink, Rob B Van der Luijt, Cornelis J M Lips
Hereditary Cancer in Clinical Practice|March 13, 2010
Von hippel-lindau diseaseFrederik J Hes, Jo Wm Höppener, Rob B van der Luijt, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Madelung deformity in a girl with a novel and de novo mutation in the GNAS genePatrick Rump, Jan D H Jongbloed, Birgit Sikkema-Raddatz, et al.
Cancer Research|August 6, 2009
Tissue selectivity in multiple endocrine neoplasia type 1-associated tumorigenesisAna Gracanin, Koen M A Dreijerink, Rob B van der Luijt, et al.
The Journal of Clinical Endocrinology and Metabolism|February 28, 2024
Clinically Relevant Germline Variants in Children With Nonmedullary Thyroid CancerKarin van der Tuin, Dina Ruano, Jeroen Knijnenburg, et al.
European Journal of Cancer (Oxford, England : 1990)|June 16, 2005
A prospective study on predictive factors linked to the presence of BRCA1 and BRCA2 mutations in breast cancer patientsCarla C Wárlám-Rodenhuis, Veronica C M Koot, Rob B van der Luijt, et al.
American Journal of Medical Genetics. Part A|June 25, 2016
Macrosomia, obesity, and macrocephaly as first clinical presentation of PHP1b caused by STX16 deletionIris M de Lange, Annemarie A Verrijn Stuart, Rob B van der Luijt, et al.
Hereditary Cancer in Clinical Practice|January 20, 2021
Recontacting non-BRCA1/2 breast cancer patients for germline CHEK2 c.1100del pathogenic variant testing: uptake and patient experiencesMary E Velthuizen, Rob B van der Luijt, Beja J de Vries, et al.
Journal of Genetic Counseling|November 30, 2012
Acceptance of genetic counseling and testing in a hospital-based series of patients with gynecological cancerNicky Dekker, Eleonora B L van Dorst, Rob B van der Luijt, et al.
The Journal of Clinical Endocrinology and Metabolism|January 15, 2002
Atypical MEN type 2B associated with two germline RET mutations on the same allele not involving codon 918Fred H Menko, Rob B van der Luijt, Irene A J de Valk, et al.
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