Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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1 Online-Ressource.
- Sprache
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Englisch
- Erschienen in
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Congenital hydrocephalus: new Mendelian mutations and evidence for oligogenic inheritance ; volume:17 ; number:1 ; day:2 ; month:3 ; year:2023 ; pages:1-14 ; date:12.2023
Human genomics ; 17, Heft 1 (2.3.2023), 1-14, 12.2023
- Urheber
-
Jacquemin, Valerie
Versbraegen, Nassim
Duerinckx, Sarah
Massart, Annick
Soblet, Julie
Perazzolo, Camille
Deconinck, Nicolas
Brischoux-Boucher, Elise
De Leener, Anne
Revencu, Nicole
Janssens, Sandra
Moorgat, Stèphanie
Blaumeiser, Bettina
Avela, Kristiina
Touraine, Renaud
Abou Jaoude, Imad
Keymolen, Kathelijn
Saugier-Veber, Pascale
Lenaerts, Tom
Abramowicz, Marc
Pirson, Isabelle
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
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10.1186/s40246-023-00464-w
- URN
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urn:nbn:de:101:1-2023121813562122622029
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:37 MESZ
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Beteiligte
- Jacquemin, Valerie
- Versbraegen, Nassim
- Duerinckx, Sarah
- Massart, Annick
- Soblet, Julie
- Perazzolo, Camille
- Deconinck, Nicolas
- Brischoux-Boucher, Elise
- De Leener, Anne
- Revencu, Nicole
- Janssens, Sandra
- Moorgat, Stèphanie
- Blaumeiser, Bettina
- Avela, Kristiina
- Touraine, Renaud
- Abou Jaoude, Imad
- Keymolen, Kathelijn
- Saugier-Veber, Pascale
- Lenaerts, Tom
- Abramowicz, Marc
- Pirson, Isabelle
- SpringerLink (Online service)
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trioPhaser: using Mendelian inheritance logic to improve genomic phasing of trios
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