Additional file 6: of Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies
- Moilanen, Jukka
- Veltman, Joris A.
- Alenezi, Njood
- Netea, Mihai G.
- Faqeih, Eissa A.
- Al-Hussaini, Abdulrahman A.
- Yilmaz, Elanur
- Alzahrani, Mofareh S.
- Potjewijd, Judith
- Keski-Filppula, Riikka
- Mensenkamp, Arjen R.
- Lelieveld, Stefan H.
- Henriet, Stefanie S.
- Hoppenreijs, Esther P.
- Zafeiropoulou, Dimitra
- Alsaad, Alaa B.
- Van Well, Gijs T. J.
- Almanjomi, Fahad
- Alidrissi, Eman
- MacKenzie, Marius A.
- Lone, Khurram
- Gilissen, Christian
- Nelen, Marcel
- Simon, Anna
- Alghamdi, Hamza A.
- Arts, Peer
- Asery, Ali
- Van Paassen, Pieter
- Ballourah, Walid
- Wagner, Anja
- Hortillosa, Sarah
- Hoischen, Alexander
- Hehir-Kwa, Jayne Y.
- Van De Vorst, Maartje
- Vreeburg, Maaike
- Aljubab, Hadeel A.
- Simons, Annet
- Stokowy, Tomasz
- Zonneveld-Huijssoon, Evelien
- Habazi, Murad K.
- Kerkhofs, Chantal H.
- Gerkes, Erica
- Alsaleem, Badr
- Ten Oever, Jaap
- Van Zelst-Stams, Wendy A. G.
- Van De Veerdonk, Frank L.
- Van Aerde, Koen J.
- Andijani, Abdulrahman A.
- Van Deuren, Marcel
- Van Der Flier, Michiel
- Schuurs-Hoeijmakers, Janneke H. M.
- Bleeker-Rovers, Chantal P.
- Radboud University Nijmegen Medical Centre
- University of Oulu
DOIAbstract
Table S6. Information on all large >â 5-Mb homozygous regions per patient, detected in the exome. Of each region, the genomic location, size, % homozygous variants, and the detected mutation are provided. (XLSX 158 kb
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