- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
Rare copy-number variants as modulators of common disease susceptibility ; volume:16 ; number:1 ; day:8 ; month:1 ; year:2024 ; pages:1-24 ; date:12.2024
Genome medicine ; 16, Heft 1 (8.1.2024), 1-24, 12.2024
- Urheber
-
Auwerx, Chiara
Jõeloo, Maarja
Sadler, Marie C.
Tesio, Nicolò
Ojavee, Sven
Clark, Charlie J.
Mägi, Reedik
Reymond, Alexandre
Kutalik, Zoltán
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s13073-023-01265-5
- URN
-
urn:nbn:de:101:1-2024031921310400243691
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
- 14.08.2025, 10:55 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
- Auwerx, Chiara
- Jõeloo, Maarja
- Sadler, Marie C.
- Tesio, Nicolò
- Ojavee, Sven
- Clark, Charlie J.
- Mägi, Reedik
- Reymond, Alexandre
- Kutalik, Zoltán
- SpringerLink (Online service)
Ähnliche Objekte (12)
CCL3L1 copy number, CCR5genotype and susceptibility to tuberculosis
E2F1 germline copy number variations and melanoma susceptibility
Functional consequences of copy number variants in miscarriage
Germline copy number variants and endometrial cancer risk
Identification of copy number variants from exome sequence data
LILRA6 copy number variation correlates with susceptibility to atopic dermatitis
Impact of constitutional copy number variants on biological pathway evolution
Genetic copy number variants in myocardial infarction patients with hyperlipidemia
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Clinical interpretation of copy number variants in the human genome
Genomic variability in Mexican chicken population using copy number variants
CNVDeep: deep association of copy number variants with neurocognitive disorders
CCL3L1 copy number, CCR5genotype and susceptibility to tuberculosis
E2F1 germline copy number variations and melanoma susceptibility
Functional consequences of copy number variants in miscarriage
Germline copy number variants and endometrial cancer risk
Identification of copy number variants from exome sequence data
LILRA6 copy number variation correlates with susceptibility to atopic dermatitis
Impact of constitutional copy number variants on biological pathway evolution
Genetic copy number variants in myocardial infarction patients with hyperlipidemia
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Clinical interpretation of copy number variants in the human genome
Genomic variability in Mexican chicken population using copy number variants
CNVDeep: deep association of copy number variants with neurocognitive disorders
CCL3L1 copy number, CCR5genotype and susceptibility to tuberculosis
E2F1 germline copy number variations and melanoma susceptibility
Functional consequences of copy number variants in miscarriage
Germline copy number variants and endometrial cancer risk
Identification of copy number variants from exome sequence data
LILRA6 copy number variation correlates with susceptibility to atopic dermatitis
Impact of constitutional copy number variants on biological pathway evolution
Genetic copy number variants in myocardial infarction patients with hyperlipidemia
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Clinical interpretation of copy number variants in the human genome
Genomic variability in Mexican chicken population using copy number variants