Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1432-1203
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU ; volume:136 ; number:4 ; day:10 ; month:3 ; year:2017 ; pages:463-479 ; date:4.2017
Human genetics; 136, Heft 4 (10.3.2017), 463-479, 4.2017
- Contributor
-
Depienne, Christel
Nava, Caroline
Keren, Boris
Heide, Solveig
Rastetter, Agnès
Passemard, Sandrine
Chantot-Bastaraud, Sandra
Moutard, Marie-Laure
Agrawal, Pankaj B.
VanNoy, Grace
Stoler, Joan M.
Amor, David J.
Billette de Villemeur, Thierry
Doummar, Diane
Alby, Caroline
Cormier-Daire, Valérie
Garel, Catherine
Marzin, Pauline
Scheidecker, Sophie
Saint-Martin, Anne de
Hirsch, Edouard
Korff, Christian
Bottani, Armand
Faivre, Laurence
Verloes, Alain
Orzechowski, Christine
Burglen, Lydie
Leheup, Bruno
Roume, Joelle
Andrieux, Joris
Sheth, Frenny
Datar, Chaitanya
Parker, Michael J.
Pasquier, Laurent
Odent, Sylvie
Naudion, Sophie
Delrue, Marie-Ange
Caignec, Cédric Le
Vincent, Marie
Isidor, Bertrand
Renaldo, Florence
Stewart, Fiona
Toutain, Annick
Koehler, Udo
Häckl, Birgit
Stülpnagel, Celina von
Kluger, Gerhard
Møller, Rikke S.
Pal, Deb
Jonson, Tord
Soller, Maria
Verbeek, Nienke E.
Haelst, Mieke M. van
Kovel, Carolien de
Koeleman, Bobby
Monroe, Glen
van Haaften, Gijs
Attié-Bitach, Tania
Boutaud, Lucile
Héron, Delphine
Mignot, Cyril
SpringerLink (Online service)
- DOI
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10.1007/s00439-017-1772-0
- URN
-
urn:nbn:de:1111-201704113162
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:46 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Depienne, Christel
- Nava, Caroline
- Keren, Boris
- Heide, Solveig
- Rastetter, Agnès
- Passemard, Sandrine
- Chantot-Bastaraud, Sandra
- Moutard, Marie-Laure
- Agrawal, Pankaj B.
- VanNoy, Grace
- Stoler, Joan M.
- Amor, David J.
- Billette de Villemeur, Thierry
- Doummar, Diane
- Alby, Caroline
- Cormier-Daire, Valérie
- Garel, Catherine
- Marzin, Pauline
- Scheidecker, Sophie
- Saint-Martin, Anne de
- Hirsch, Edouard
- Korff, Christian
- Bottani, Armand
- Faivre, Laurence
- Verloes, Alain
- Orzechowski, Christine
- Burglen, Lydie
- Leheup, Bruno
- Roume, Joelle
- Andrieux, Joris
- Sheth, Frenny
- Datar, Chaitanya
- Parker, Michael J.
- Pasquier, Laurent
- Odent, Sylvie
- Naudion, Sophie
- Delrue, Marie-Ange
- Caignec, Cédric Le
- Vincent, Marie
- Isidor, Bertrand
- Renaldo, Florence
- Stewart, Fiona
- Toutain, Annick
- Koehler, Udo
- Häckl, Birgit
- Stülpnagel, Celina von
- Kluger, Gerhard
- Møller, Rikke S.
- Pal, Deb
- Jonson, Tord
- Soller, Maria
- Verbeek, Nienke E.
- Haelst, Mieke M. van
- Kovel, Carolien de
- Koeleman, Bobby
- Monroe, Glen
- van Haaften, Gijs
- Attié-Bitach, Tania
- Boutaud, Lucile
- Héron, Delphine
- Mignot, Cyril
- SpringerLink (Online service)
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Phenotypic and molecular characterization of pleiotropic phenotypes in Arabidopsis and barley $mlo$ mutants
Adult reversal of cognitive phenotypes in neurodevelopmental disorders
Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in a zebrafish model
Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in two zebrafish models
Pleiotropic contribution of rbfox1 to psychiatric and neurodevelopmental phenotypes in a zebrafish model