Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
Isolated dentinogenesis imperfecta: Novel DSPP variants and insights on genetic counselling ; volume:28 ; number:5 ; day:17 ; month:4 ; year:2024 ; pages:1-8 ; date:5.2024
Clinical oral investigations ; 28, Heft 5 (17.4.2024), 1-8, 5.2024
- Creator
-
Hassib, Nehal F.
Mehrez, Mennat
Mostafa, Mostafa I.
Abdel-Hamid, Mohamed S.
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1007/s00784-024-05636-z
- URN
-
urn:nbn:de:101:1-2408060900288.902086760962
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:46 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
- Hassib, Nehal F.
- Mehrez, Mennat
- Mostafa, Mostafa I.
- Abdel-Hamid, Mohamed S.
- SpringerLink (Online service)
Other Objects (12)
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta
Amelogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta : Mit bes. Berücks. d. Dentinogenesis imperfecta
La perfecta imperfecta
Ventriculosubgaleal shunt placement for hydrocephalus in osteogenesis imperfecta with novel compound heterozygous CRTAP variants
Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants
Dominant VPS16 pathogenic variants: not only isolated dystonia
CACNA1B gene variants in adult-onset isolated focal dystonia
Verba imperfecta: Quiescentia & Defectiva.
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta
Amelogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta : Mit bes. Berücks. d. Dentinogenesis imperfecta
La perfecta imperfecta
Ventriculosubgaleal shunt placement for hydrocephalus in osteogenesis imperfecta with novel compound heterozygous CRTAP variants
Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants
Dominant VPS16 pathogenic variants: not only isolated dystonia
CACNA1B gene variants in adult-onset isolated focal dystonia
Verba imperfecta: Quiescentia & Defectiva.
Mutations in FKBP10 can cause a severe form of isolated Osteogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta
Amelogenesis imperfecta
Osteogenesis imperfecta
Osteogenesis imperfecta : Mit bes. Berücks. d. Dentinogenesis imperfecta
La perfecta imperfecta
Ventriculosubgaleal shunt placement for hydrocephalus in osteogenesis imperfecta with novel compound heterozygous CRTAP variants
Canine models of human amelogenesis imperfecta: identification of novel recessive ENAM and ACP4 variants
Dominant VPS16 pathogenic variants: not only isolated dystonia
CACNA1B gene variants in adult-onset isolated focal dystonia