Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1756-994X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies ; volume:11 ; number:1 ; day:17 ; month:6 ; year:2019 ; pages:1-15 ; date:12.2019
Genome medicine ; 11, Heft 1 (17.6.2019), 1-15, 12.2019

Creator: Arts, Peer
Simons, Annet
AlZahrani, Mofareh S.
Yilmaz, Elanur
AlIdrissi, Eman
Aerde, Koen J. van
Alenezi, Njood
AlGhamdi, Hamza A.
AlJubab, Hadeel A.
Al-Hussaini, Abdulrahman A.
AlManjomi, Fahad
Alsaad, Alaa B.
Alsaleem, Badr
Andijani, Abdulrahman A.
Asery, Ali
Ballourah, Walid
Bleeker-Rovers, Chantal P.
Deuren, Marcel van
Flier, Michiel van der
Gerkes, Erica H.
Gilissen, Christian
Habazi, Murad K.
Hehir-Kwa, Jayne Y.
Henriet, Stefanie S.
Hoppenreijs, Esther P.
Hortillosa, Sarah
Kerkhofs, Chantal H.
Keski-Filppula, Riikka
Lelieveld, Stefan H.
Lone, Khurram
MacKenzie, Marius A.
Mensenkamp, Arjen R.
Moilanen, Jukka
Nelen, Marcel
Oever, Jaap ten
Potjewijd, Judith
Paassen, Pieter van
Schuurs-Hoeijmakers, Janneke H. M.
Simon, Anna
Stokowy, Tomasz
Vorst, Maartje van de
Vreeburg, Maaike
Wagner, Anja
Well, Gijs T. J. van
Zafeiropoulou, Dimitra
Zonneveld-Huijssoon, Evelien
Veltman, Joris A.
Zelst-Stams, Wendy A. G. van
Faqeih, Eissa A.
Veerdonk, Frank L. van de
Netea, Mihai G.
Hoischen, Alexander

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13073-019-0649-3

URN: urn:nbn:de:101:1-2019102200075758922660

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:26 AM CEST

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Associated

Arts, Peer
Simons, Annet
AlZahrani, Mofareh S.
Yilmaz, Elanur
AlIdrissi, Eman
Aerde, Koen J. van
Alenezi, Njood
AlGhamdi, Hamza A.
AlJubab, Hadeel A.
Al-Hussaini, Abdulrahman A.
AlManjomi, Fahad
Alsaad, Alaa B.
Alsaleem, Badr
Andijani, Abdulrahman A.
Asery, Ali
Ballourah, Walid
Bleeker-Rovers, Chantal P.
Deuren, Marcel van
Flier, Michiel van der
Gerkes, Erica H.
Gilissen, Christian
Habazi, Murad K.
Hehir-Kwa, Jayne Y.
Henriet, Stefanie S.
Hoppenreijs, Esther P.
Hortillosa, Sarah
Kerkhofs, Chantal H.
Keski-Filppula, Riikka
Lelieveld, Stefan H.
Lone, Khurram
MacKenzie, Marius A.
Mensenkamp, Arjen R.
Moilanen, Jukka
Nelen, Marcel
Oever, Jaap ten
Potjewijd, Judith
Paassen, Pieter van
Schuurs-Hoeijmakers, Janneke H. M.
Simon, Anna
Stokowy, Tomasz
Vorst, Maartje van de
Vreeburg, Maaike
Wagner, Anja
Well, Gijs T. J. van
Zafeiropoulou, Dimitra
Zonneveld-Huijssoon, Evelien
Veltman, Joris A.
Zelst-Stams, Wendy A. G. van
Faqeih, Eissa A.
Veerdonk, Frank L. van de
Netea, Mihai G.
Hoischen, Alexander
SpringerLink (Online service)

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Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies

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Other Objects (12)

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Reference values for generic instruments used in routine outcome monitoring: the leiden routine outcome monitoring study

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