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Authors whose works are in public domain in at least one jurisdiction

List of works by Kornelia Neveling

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer

scientific article

Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability

scientific article

Identification of pathogenic gene variants in small families with intellectually disabled siblings by exome sequencing.

scientific article published on 11 October 2013

Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome

scientific article published on 29 April 2012

Prenatal exclusion/confirmation of Fanconi anemia via flow cytometry: a pilot study

scientific article published in January 2006

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