Skip to content
DraconiticResearch
Search Sources API
203,948 studies31 sourcesUpdated 31 min ago
Peer-reviewedLicence not statedMedizinische Genetik

Leitlinie für die molekulare und zytogenetische Diagnostik bei Prader-Willi-Syndrom und Angelman-Syndrom

  1. 1Universitätsklinikum Essen, Universität Duisburg-Essen Institut für Humangenetik Hufelandstr. 55 45147 Essen Germany

Related

  1. Parvalbumin interneurons and dentate gyrus homeostatic dysregulation shape epileptogenesis in Angelman syndrome model mice
    N. W. Ringelberg, D. W. Kipp, R. E. Mayfield +6
    bioRxivPreprintAll rights reservedFull text1 citedNeurosciencebioRxiv
  2. Vision In SyndrOmic Neurodevelopmental disorders-15q (VISiON-15q) study: eye tracking to supplement clinical examination for detection of cerebral/cortical visual impairment in children with Angelman and Duplication of 15q Syndromes
    Melinda Y. Chang, Sydney Jacobs, Katherine Granger +3
    Frontiers in human neurosciencePeer-reviewedCC BYFull textNeuroscienceEurope PMC
  3. Cortical dynamics in Angelman syndrome: novel insights from a preclinical mouse model
    Manuel Scorrano, Elena Montagni, Abenezer Tarekegne Legesse +5
    Translational PsychiatryPeer-reviewedCC BY-NC-ND 4.0Full textGenetics & genomicsPMC
  4. Aberrant accumulation of α-synuclein might be linked with the progressive motor deficits in a mouse model of Angelman syndrome
    S. Das, B. Giri, N. R. Jana
    bioRxivPreprintCC BYFull textNeurosciencebioRxiv
BibTeX
@article{beygo2026leitlinie,
  title = {{Leitlinie für die molekulare und zytogenetische Diagnostik bei Prader-Willi-Syndrom und Angelman-Syndrom}},
  author = {Jasmin Beygo},
  journal = {Medizinische Genetik},
  year = {2026},
  month = nov,
  doi = {10.1515/medgen-2026-3027},
  url = {https://doi.org/10.1515/medgen-2026-3027},
}
RIS
TY  - JOUR
TI  - Leitlinie für die molekulare und zytogenetische Diagnostik bei Prader-Willi-Syndrom und Angelman-Syndrom
AU  - Jasmin Beygo
PY  - 2026
DA  - 2026/11/06
JO  - Medizinische Genetik
DO  - 10.1515/medgen-2026-3027
UR  - https://doi.org/10.1515/medgen-2026-3027
SN  - 0936-5931
SN  - 1863-5490
ER  -