Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Array-CGH analysis in Rwandan patients presenting development delay/intellectual disability with multiple congenital anomalies ; volume:15 ; number:1 ; day:12 ; month:7 ; year:2014 ; pages:1-10 ; date:12.2014
BMC medical genetics ; 15, Heft 1 (12.7.2014), 1-10, 12.2014
- Urheber
-
Uwineza, Annette
- Beteiligte Personen und Organisationen
-
Caberg, Jean-Hubert
Hitayezu, Janvier
Hellin, Anne Cecile
Jamar, Mauricette
Dideberg, Vinciane
Rusingiza, Emmanuel K.
Bours, Vincent
Mutesa, Leon
SpringerLink (Online service)
- DOI
-
10.1186/1471-2350-15-79
- URN
-
urn:nbn:de:1111-2016081217502
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:46 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
- Uwineza, Annette
- Caberg, Jean-Hubert
- Hitayezu, Janvier
- Hellin, Anne Cecile
- Jamar, Mauricette
- Dideberg, Vinciane
- Rusingiza, Emmanuel K.
- Bours, Vincent
- Mutesa, Leon
- SpringerLink (Online service)
Ähnliche Objekte (12)
Array-CGH bei Patienten mit Intelligenzminderung
Spatial normalization of array-CGH data
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH
New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants
A statistical approach for array CGH data analysis
Korrelation von Array-CGH-Befunden und klinischem Phänotyp
Estimation of tumor heterogeneity using CGH array data
Autosomal dominant intellectual disability
CGHPRO – A comprehensive data analysis tool for array CGH
Association between craniofacial anomalies, intellectual disability and autism spectrum disorder: Western Australian population-based study
Comprehensive chromosome analysis of blastocysts before implantation using array CGH
Array-CGH bei Patienten mit Intelligenzminderung
Spatial normalization of array-CGH data
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH
New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants
A statistical approach for array CGH data analysis
Korrelation von Array-CGH-Befunden und klinischem Phänotyp
Estimation of tumor heterogeneity using CGH array data
Autosomal dominant intellectual disability
CGHPRO – A comprehensive data analysis tool for array CGH
Association between craniofacial anomalies, intellectual disability and autism spectrum disorder: Western Australian population-based study
Comprehensive chromosome analysis of blastocysts before implantation using array CGH
Array-CGH bei Patienten mit Intelligenzminderung
Spatial normalization of array-CGH data
11p11.12p12 duplication in a family with intellectual disability and craniofacial anomalies
A new look towards BAC-based array CGH through a comprehensive comparison with oligo-based array CGH
New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants
A statistical approach for array CGH data analysis
Korrelation von Array-CGH-Befunden und klinischem Phänotyp
Estimation of tumor heterogeneity using CGH array data
Autosomal dominant intellectual disability
CGHPRO – A comprehensive data analysis tool for array CGH
Association between craniofacial anomalies, intellectual disability and autism spectrum disorder: Western Australian population-based study