Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8166
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Prenatal diagnosis of 1p34.3 interstitial microdeletion by aCGH in a fetus with jaw bone abnormalities ; volume:9 ; number:1 ; day:6 ; month:10 ; year:2016 ; pages:1-5 ; date:12.2016
Molecular cytogenetics ; 9, Heft 1 (6.10.2016), 1-5, 12.2016
- Urheber
-
Dagklis, Themistoklis
- Beteiligte Personen und Organisationen
-
Papageorgiou, Elena
Siomou, Elisavet
Paspaliaris, Vassilis
Zerva, Christina
Chatzis, Panagiotis
Thomaidis, Loretta
Manolakos, Emmanouil
Papoulidis, Ioannis
SpringerLink (Online service)
- DOI
-
10.1186/s13039-016-0288-y
- URN
-
urn:nbn:de:1111-2016110612283
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:59 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
- Dagklis, Themistoklis
- Papageorgiou, Elena
- Siomou, Elisavet
- Paspaliaris, Vassilis
- Zerva, Christina
- Chatzis, Panagiotis
- Thomaidis, Loretta
- Manolakos, Emmanouil
- Papoulidis, Ioannis
- SpringerLink (Online service)
Ähnliche Objekte (12)
A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH
3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities
A fetus with 19q13.11 microdeletion presenting with intrauterine growth restriction and multiple cystic kidney a
Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities
M-CGH: Analysing microarray-based CGH experiments
Lingual and Jaw Kinematic Abnormalities Precede Speech and Swallowing Impairments in ALS
JAW
Chromosome 15q24 microdeletion syndrome
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome
J.A.W. Kohlmeyer, vormals: J.A.W. Kohlmeyer & Sohn
A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH
3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities
A fetus with 19q13.11 microdeletion presenting with intrauterine growth restriction and multiple cystic kidney a
Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities
M-CGH: Analysing microarray-based CGH experiments
Lingual and Jaw Kinematic Abnormalities Precede Speech and Swallowing Impairments in ALS
JAW
Chromosome 15q24 microdeletion syndrome
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome
J.A.W. Kohlmeyer, vormals: J.A.W. Kohlmeyer & Sohn
A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH
3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities
A fetus with 19q13.11 microdeletion presenting with intrauterine growth restriction and multiple cystic kidney a
Prenatal diagnosis of 17q12 microdeletion and microduplication syndrome in fetuses with congenital renal abnormalities
M-CGH: Analysing microarray-based CGH experiments
Lingual and Jaw Kinematic Abnormalities Precede Speech and Swallowing Impairments in ALS
JAW
Chromosome 15q24 microdeletion syndrome
Microdeletion of 6q16.1 encompassing EPHA7 in a child with mild neurological abnormalities and dysmorphic features: case report
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report
Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome