Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Human PTCHD3 nulls: rare copy number and sequence variants suggest a non-essential gene ; volume:12 ; number:1 ; day:26 ; month:3 ; year:2011 ; pages:1-9 ; date:12.2011
BMC medical genetics ; 12, Heft 1 (26.3.2011), 1-9, 12.2011
- Creator
-
Ghahramani Seno, Mohammad M.
- Contributor
-
Kwan, Benjamin YM
Lee-Ng, Ka Ki M.
Moessner, Rainald
Lionel, Anath C.
Marshall, Christian R.
Scherer, Stephen W.
SpringerLink (Online service)
- DOI
-
10.1186/1471-2350-12-45
- URN
-
urn:nbn:de:1111-2016071514357
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:48 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
- Ghahramani Seno, Mohammad M.
- Kwan, Benjamin YM
- Lee-Ng, Ka Ki M.
- Moessner, Rainald
- Lionel, Anath C.
- Marshall, Christian R.
- Scherer, Stephen W.
- SpringerLink (Online service)
Other Objects (12)
Rare variants analyses suggest novel cleft genes in the African population
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
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
Rare copy-number variants as modulators of common disease susceptibility
CNVDeep: deep association of copy number variants with neurocognitive disorders
Measurement of absolute copy number variation reveals association with essential hypertension
Rare variants analyses suggest novel cleft genes in the African population
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
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
Rare copy-number variants as modulators of common disease susceptibility
CNVDeep: deep association of copy number variants with neurocognitive disorders
Measurement of absolute copy number variation reveals association with essential hypertension
Rare variants analyses suggest novel cleft genes in the African population
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
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
Rare copy-number variants as modulators of common disease susceptibility
CNVDeep: deep association of copy number variants with neurocognitive disorders