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X
Čejnová, Vlasta
6  Ergebnisse:
Personensuche X
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1

Czech family confirms the new 1p36.13‐1p36.12 microdeletion..:

Seeman, Pavel ; Čejnová, Vlasta ; Černá, Šárka...
Clinical Genetics.  102 (2022)  3 - p. 244-245 , 2022
Link: https://doi.org/10.1111/..
 
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2

The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:

Safka Brozkova, Dana ; Uhrova Meszarosova, Anna ; Lassuthova, Petra...
Genes.  12 (2021)  5 - p. 684 , 2021
Link: https://doi.org/10.3390/..
 
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3

Spectrum and frequencies of non GJB2 gene mutations in Czec..:

Safka Brozkova, Dana ; Poisson Marková, Simona ; Mészárosová, Anna Uhrová...
Clinical Genetics.  98 (2020)  6 - p. 548-554 , 2020
Link: https://doi.org/10.1111/..
 
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4

The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:

Safka Brozkova, Dana ; Uhrova Meszarosova, Anna ; Lassuthova, Petra...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147375/.  , 2021
Link: http://www.ncbi.nlm.nih...
 
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5

The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:

Dana Safka Brozkova ; Anna Uhrova Meszarosova ; Petra Lassuthova...
https://www.mdpi.com/2073-4425/12/5/684.  , 2021
Link: https://doi.org/10.3390/..
 
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6

The Cause of Hereditary Hearing Loss in GJB2 Heterozygotes—..:

Dana Safka Brozkova ; Anna Uhrova Meszarosova ; Petra Lassuthova...
Human Genomics and Genetic Diseases.  , 2021
Link: https://doi.org/10.3390/..
 
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