Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1471-2350
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
online resource.
- Bibliographic citation
-
Whole exome sequencing highlights variants in association with Keratoconus in Jordanian families ; volume:21 ; number:1 ; day:4 ; month:9 ; year:2020 ; pages:1-6 ; date:12.2020
BMC medical genetics ; 21, Heft 1 (4.9.2020), 1-6, 12.2020
- Creator
-
Froukh, Tawfiq
Hawwari, Ammar
Al Zubi, Khalid
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s12881-020-01112-z
- URN
-
urn:nbn:de:101:1-2020102520472152555638
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:29 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
- Froukh, Tawfiq
- Hawwari, Ammar
- Al Zubi, Khalid
- SpringerLink (Online service)
Other Objects (12)
Identification of genetic variants in two families with Keratoconus
Exome variants associated with asthma and allergy
Keratoconus International Consortium (KIC)- advancing keratoconus research
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families
Identification of copy number variants from exome sequence data
Annotation of human exome gene variants with consensus pathogenicity
Identifying rare variants from exome scans: the GAW17 experience
Keratoconus Treatment Algorithm
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus
Exome-wide analysis implicates rare protein-altering variants in human handedness
Identification of genetic variants in two families with Keratoconus
Exome variants associated with asthma and allergy
Keratoconus International Consortium (KIC)- advancing keratoconus research
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families
Identification of copy number variants from exome sequence data
Annotation of human exome gene variants with consensus pathogenicity
Identifying rare variants from exome scans: the GAW17 experience
Keratoconus Treatment Algorithm
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus
Exome-wide analysis implicates rare protein-altering variants in human handedness
Identification of genetic variants in two families with Keratoconus
Exome variants associated with asthma and allergy
Keratoconus International Consortium (KIC)- advancing keratoconus research
USH2A gene variants cause Keratoconus and Usher syndrome phenotypes in Pakistani families
Identification of copy number variants from exome sequence data
Annotation of human exome gene variants with consensus pathogenicity
Identifying rare variants from exome scans: the GAW17 experience
Keratoconus Treatment Algorithm
EXCAVATOR: detecting copy number variants from whole-exome sequencing data
Case-control association between CCT-associated variants and keratoconus in a Saudi Arabian population
Investigation of VSX1 sequence variants in South Indian patients with sporadic cases of keratoconus