Han G. Brunner

Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).

T. Keith, L. Blonden, D. Callen, 1990, Journal of Medical Genetics.

Detailed mapping, mutation analysis, and intragenic polymorphism identification in candidate Noonan syndrome genes MYL2,DCN, EPS8, andRPL6

A. Ion, S. Dabora, I. Burgt, 2000, Journal of medical genetics.

De novo WNT5A‐associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype

H. Kayserili, H. Venselaar, H. Yntema, 2015, Clinical genetics.

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

L. Vissers, B. D. de Vries, E. Eichler, 2008, Journal of Medical Genetics.