- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
1 Online-Ressource.
- Language
-
Englisch
- Bibliographic citation
-
From uncertain to certain—how to proceed with variants of uncertain significance ; volume:29 ; number:1 ; day:16 ; month:8 ; year:2024 ; pages:1-7 ; date:12.2024
Middle East Fertility Society journal / Middle East Fertility Society ; 29, Heft 1 (16.8.2024), 1-7, 12.2024
- Creator
-
Banerjee, Emili
Pal, Suman
Biswas, Abhijit
Bhattacharjee, Koutilya
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s43043-024-00202-9
- URN
-
urn:nbn:de:101:1-2411032113269.117946004447
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:30 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
- Banerjee, Emili
- Pal, Suman
- Biswas, Abhijit
- Bhattacharjee, Koutilya
- SpringerLink (Online service)
Other Objects (12)
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
Government spending multipliers in (un)certain times
Government spending multipliers in (un)certain times
Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?
Functional assessment of IDUA variants of uncertain significance identified by newborn screening
"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders"
Un/certain futures - Rollen des Designs in gesellschaftlichen Transformationsprozessen
Un/Certain Futures - Rollen des Designs in gesellschaftlichen Transformationsprozessen
Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome
Correction: “Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders”
Functional assessment of missense variants of uncertain significance in the cancer susceptibility gene PALB2
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
Government spending multipliers in (un)certain times
Government spending multipliers in (un)certain times
Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?
Functional assessment of IDUA variants of uncertain significance identified by newborn screening
"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders"
Un/certain futures - Rollen des Designs in gesellschaftlichen Transformationsprozessen
Un/Certain Futures - Rollen des Designs in gesellschaftlichen Transformationsprozessen
Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome
Correction: “Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders”
Functional assessment of missense variants of uncertain significance in the cancer susceptibility gene PALB2
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
KCNC2 variants of uncertain significance are also associated to various forms of epilepsy
Government spending multipliers in (un)certain times
Government spending multipliers in (un)certain times
Variants of uncertain significance in BRCA: a harbinger of ethical and policy issues to come?
Functional assessment of IDUA variants of uncertain significance identified by newborn screening
"Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders"
Un/certain futures - Rollen des Designs in gesellschaftlichen Transformationsprozessen
Un/Certain Futures - Rollen des Designs in gesellschaftlichen Transformationsprozessen
Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome
Correction: “Re-evaluation of variants of uncertain significance in patients with hereditary arrhythmogenic disorders”