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3. A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

4. Innovative method for reducing uninformative calls in non-invasive prenatal testing

7. Detection of contamination in noninvasive prenatal fetal gender test

14. Combination of Expert Guidelines-based and Machine Learning-based Approaches Leads to Superior Accuracy of Automated Prediction of Clinical Effect of Copy Number Variations

17. Comparison of microbial diversity of respiratory tract between COVID-19 patients and healthy population.

25. A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia

27. A Common Founder Effect of the Splice Site Variant c.-23+1G>A in GJB2 Gene Causing Autosomal Recessive Deafness 1A (DFNB1A) in Eurasia

31. Analysis of forensically used autosomal short tandem repeat markers in Polish and neighboring populations

36. Spinal muscular atrophy caused by a novel Alu ‐mediated deletion of exons 2a‐5 in SMN1 undetectable with routine genetic testing

37. Association of CD33 rs3865444:C˃A polymorphism with a reduced risk of late-onset Alzheimer's disease in Slovaks is limited to subjects carrying the APOE ε4 allele

41. Absence of a Significant Interaction of Two Common NOS1 and 5-HTT Polymorphisms on Sensorimotor Gating in Humans.

46. Additional file 1: Table S1. of Population structure and dispersal routes of an invasive parasite, Fascioloides magna, in North America and Europe

48. Additional file 2: Tables S4-S5. of Population structure and dispersal routes of an invasive parasite, Fascioloides magna, in North America and Europe

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