LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1755-8794
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
-
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosis ; volume:15 ; number:1 ; day:15 ; month:7 ; year:2022 ; pages:1-15 ; date:12.2022
BMC medical genomics ; 15, Heft 1 (15.7.2022), 1-15, 12.2022
- Creator
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Farncombe, Kirsten M.
Thain, Emily
Barnett-Tapia, Carolina
Sadeghian, Hamid
Kim, Raymond H.
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12920-022-01304-x
- URN
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urn:nbn:de:101:1-2022092106365062735186
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:32 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Farncombe, Kirsten M.
- Thain, Emily
- Barnett-Tapia, Carolina
- Sadeghian, Hamid
- Kim, Raymond H.
- SpringerLink (Online service)
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Genetic and Pathogenetic Aspects of Noonan Syndrome and Related Disorders
Overlap-Syndrome
Short rib-polydactyly syndrome (Saldino-Noonan type) undetected by standard prenatal genetic testing
Right ventricular morphology and function in patients with Noonan’s syndrome after pulmonary intervention
Personality and Psychopathology in Adults with Noonan Syndrome
Novel therapeutic perspectives in Noonan syndrome and RASopathies
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MAPK activation in mature cataract associated with Noonan syndrome
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