Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: Molecular Syndromology 2010; 1: 99-112.
- Schlagwort
-
-
Krebs
Onkologie
- Ereignis
-
Veröffentlichung
- (wo)
-
Erlangen
- (wer)
-
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (wann)
-
2013
- Beteiligte Personen und Organisationen
-
Ekici, Arif Bülent
Hilfinger, D.
Jatzwauk, M.
Thiel, Christian
Wenzel, Dieter
Lorenz, Imke
Boltshauser, E.
Goecke, Tamme W.
Staatz, G.
Morris-Rosendahl, D. J.
Sticht, Heinrich
Hehr, U.
Reis, André
Rauch, Anita
- URN
-
urn:nbn:de:bvb:29-opus-44866
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:55 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Ekici, Arif Bülent
- Hilfinger, D.
- Jatzwauk, M.
- Thiel, Christian
- Wenzel, Dieter
- Lorenz, Imke
- Boltshauser, E.
- Goecke, Tamme W.
- Staatz, G.
- Morris-Rosendahl, D. J.
- Sticht, Heinrich
- Hehr, U.
- Reis, André
- Rauch, Anita
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Entstanden
- 2013
Ähnliche Objekte (12)
Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases
Multidisciplinary treatment of non-syndromic oligodontia
Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders
Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
A comprehensive molecular analysis of genes implicated in syndromic and non-syndromic craniosynostosis
The role of DNA methylation in syndromic and non-syndromic congenital heart disease
OR11-002 - Mutations in MVK cause non-syndromic RP
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
Deciphering similarities and differences in the neuroanatomical correlates of syndromic and non-syndromic neurodevelopmental disorders
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
Craniofacial and Oral Manifestations of Non-Syndromic Hypodontia: A Review
Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases
Multidisciplinary treatment of non-syndromic oligodontia
Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders
Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
A comprehensive molecular analysis of genes implicated in syndromic and non-syndromic craniosynostosis
The role of DNA methylation in syndromic and non-syndromic congenital heart disease
OR11-002 - Mutations in MVK cause non-syndromic RP
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
Deciphering similarities and differences in the neuroanatomical correlates of syndromic and non-syndromic neurodevelopmental disorders
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy
Craniofacial and Oral Manifestations of Non-Syndromic Hypodontia: A Review
Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases
Multidisciplinary treatment of non-syndromic oligodontia
Bariatric Surgery for Monogenic Non-syndromic and Syndromic Obesity Disorders
Characterization of germ cell differentiation in the male mouse through single-cell RNA sequencing
Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families
A comprehensive molecular analysis of genes implicated in syndromic and non-syndromic craniosynostosis
The role of DNA methylation in syndromic and non-syndromic congenital heart disease
OR11-002 - Mutations in MVK cause non-syndromic RP
Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients
Deciphering similarities and differences in the neuroanatomical correlates of syndromic and non-syndromic neurodevelopmental disorders
Novel pathogenic variant in MED12 causing non-syndromic dilated cardiomyopathy