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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Syndrome and PRKDC[original query]
Copy number variation analysis and targeted NGS in 77 families with suspected Lynch syndrome reveals novel potential causative genes.
International journal of cancer 2018 Jul .
Kayser Katrin, Degenhardt Franziska, Holzapfel Stefanie, Horpaopan Sukanya, Peters Sophia, Spier Isabel, Morak Monika, Vangala Deepak, Rahner Nils, von Knebel-Doeberitz Magnus, Schackert Hans K, Engel Christoph, Büttner Reinhard, Wijnen Juul, Doerks Tobias, Bork Peer, Moebus Susanne, Herms Stefan, Fischer Sascha, Hoffmann Per, Aretz Stefan, Steinke-Lange Vere
Genetic Variant Screening of DNA Repair Genes in Myelodysplastic Syndrome Identifies a Novel Mutation in the XRCC2 Gene.
Oncology research and treatment 2019 Mar 1-6.
Valka Jan, Vesela Jitka, Votavova Hana, Dostalova-Merkerova Michaela, Urbanova Zuzana, Jonasova Anna, Cermak Jaroslav, Belickova Moni
Investigation of Cerebellar Abiotrophy (CA), Lavender Foal Syndrome (LFS), and Severe Combined Immunodeficiency (SCID) Variants in a Cohort of Three MENA Region Horse Breeds.
Genes 2021 12 12 (12): .
Ayad Abdelhanine, Almarzook Saria, Besseboua Omar, Aissanou Sofiane, Piórkowska Katarzyna, Musia? Adrianna D, Stefaniuk-Szmukier Monika, Ropka-Molik Katarzy
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