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1.
Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.
Clin Genet
; 98(6): 548-554, 2020 12.
Article
in English
| MEDLINE | ID: mdl-32860223
2.
Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.
Eur Arch Otorhinolaryngol
; 276(12): 3353-3358, 2019 Dec.
Article
in English
| MEDLINE | ID: mdl-31552524
3.
Lignocellulosic Bioethanol and Biobutanol as a Biocomponent for Diesel Fuel.
Materials (Basel)
; 14(19)2021 Sep 26.
Article
in English
| MEDLINE | ID: mdl-34639994
4.
Use of Dicyclopentadiene and Methyl Dicyclopentadiene for the Synthesis of Unsaturated Polyester Resins.
Polymers (Basel)
; 13(18)2021 Sep 16.
Article
in English
| MEDLINE | ID: mdl-34578034
5.
Advanced Biofuels Based on Fischer-Tropsch Synthesis for Applications in Diesel Engines.
Materials (Basel)
; 14(11)2021 Jun 04.
Article
in English
| MEDLINE | ID: mdl-34199859
6.
Advanced Biofuels Based on Fischer-Tropsch Synthesis for Applications in Gasoline Engines.
Materials (Basel)
; 14(11)2021 Jun 07.
Article
in English
| MEDLINE | ID: mdl-34200359
7.
Two types of recessive hereditary spastic paraplegia in Roma patients in compound heterozygous state; no ethnically prevalent variant found.
Neurosci Lett
; 721: 134800, 2020 03 16.
Article
in English
| MEDLINE | ID: mdl-32007496
8.
Variant c.2158-2A>G in MANBA is an important and frequent cause of hereditary hearing loss and beta-mannosidosis among the Czech and Slovak Roma population- evidence for a new ethnic-specific variant.
Orphanet J Rare Dis
; 15(1): 222, 2020 08 26.
Article
in English
| MEDLINE | ID: mdl-32847582
9.
Fanconi anemia with biallelic FANCD1/BRCA2 mutations - Case report of a family with three affected children.
Eur J Med Genet
; 59(3): 152-7, 2016 Mar.
Article
in English
| MEDLINE | ID: mdl-26657402
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