Items where authors include "Zurcher, V."

Article

Kruszka, P., Berger, S.I., Casa, V. et al. (32 more authors) (2019) Cohesin complex-associated holoprosencephaly. Brain, 142 (9). pp. 2631-2643. ISSN 0006-8950

Koczkowska, M., Chen, Y., Callens, T. et al. (72 more authors) (2018) Genotype-Phenotype Correlation in NF1: Evidence for a More Severe Phenotype Associated with Missense Mutations Affecting NF1 Codons 844-848. American Journal of Human Genetics, 102 (1). pp. 69-87. ISSN 0002-9297