Litcius/Paper detail

Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome

Alexander J.M. Dingemans, Diante E. Stremmelaar, Roos van der Donk, Lisenka E.L.M. Vissers, David A. Koolen, Patrick Rump, Jayne Y. Hehir‐Kwa, Bert B.A. de Vries

2021European Journal of Human Genetics14 citationsDOIOpen Access PDF

Topics & Concepts

Deletion syndromeBiologyGeneticsComputational biologyEvolutionary biologyPhenotypeGeneCongenital heart defects researchGenomic variations and chromosomal abnormalitiesGenomics and Rare Diseases