- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1755-8166
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
6q16.3q23.3 duplication associated with Prader-Willi-like syndrome ; volume:8 ; number:1 ; day:25 ; month:6 ; year:2015 ; pages:1-5 ; date:12.2015
Molecular cytogenetics ; 8, Heft 1 (25.6.2015), 1-5, 12.2015
- Urheber
-
Desch, Laurent
Marle, Nathalie
Mosca-Boidron, Anne-Laure
Faivre, Laurence
Eliade, Marie
Payet, Muriel
Ragon, Clemence
Thevenon, Julien
Aral, Bernard
Ragot, Sylviane
Ardalan, Azarnouche
Dhouibi, Nabila
Bensignor, Candace
Thauvin-Robinet, Christel
El Chehadeh, Salima
Callier, Patrick
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13039-015-0151-6
- URN
-
urn:nbn:de:101:1-2021081422291565121201
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 11:04 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
- Desch, Laurent
- Marle, Nathalie
- Mosca-Boidron, Anne-Laure
- Faivre, Laurence
- Eliade, Marie
- Payet, Muriel
- Ragon, Clemence
- Thevenon, Julien
- Aral, Bernard
- Ragot, Sylviane
- Ardalan, Azarnouche
- Dhouibi, Nabila
- Bensignor, Candace
- Thauvin-Robinet, Christel
- El Chehadeh, Salima
- Callier, Patrick
- SpringerLink (Online service)
Ähnliche Objekte (12)
Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
Sleep Consequences of Prader-Willi Syndrome
Ovarian cyst torsion in Prader-Willi Syndrome
Prader-Willi syndrome: A primer for clinicians
The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome
Partial CHARGE syndrome with bilateral retinochoroidal colobomas associated with 7q11.23 duplication syndrome: case report
Prader-Willi syndrome : selected research and management issues
Orthopedic manifestations in children with Prader-Willi syndrome
Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry
Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
Sleep Consequences of Prader-Willi Syndrome
Ovarian cyst torsion in Prader-Willi Syndrome
Prader-Willi syndrome: A primer for clinicians
The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome
Partial CHARGE syndrome with bilateral retinochoroidal colobomas associated with 7q11.23 duplication syndrome: case report
Prader-Willi syndrome : selected research and management issues
Orthopedic manifestations in children with Prader-Willi syndrome
Incidence of strabismus, strabismus surgeries, and other vision conditions in Prader-Willi syndrome: data from the Global Prader-Willi Syndrome Registry
Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy
Management of Prader-Willi syndrome
Management of Prader-Willi syndrome
Distinct promoter regions of the oxytocin receptor gene are hypomethylated in Prader-Willi syndrome and in Prader-Willi syndrome associated psychosis
Sleep Consequences of Prader-Willi Syndrome
Ovarian cyst torsion in Prader-Willi Syndrome
Prader-Willi syndrome: A primer for clinicians
The Prader-Willi syndrome Profile: validation of a new measure of behavioral and emotional problems in Prader-Willi syndrome
Partial CHARGE syndrome with bilateral retinochoroidal colobomas associated with 7q11.23 duplication syndrome: case report
Prader-Willi syndrome : selected research and management issues
Orthopedic manifestations in children with Prader-Willi syndrome