
11 Artykułów
Review
Original Article
Variants in mitochondrial tRNA gene may not be associated with thyroid carcinoma
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CYP2D6 allele distribution in Macedonians, Albanians and Romanies in the Republic of Macedonia
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Association between the catechol-o-methyltransferase val158met polymorphism with susceptibility and severity of carpal tunnel syndrome
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Association of the ACE rs4646994 and rs4341 polymorphisms with the progression of carotid atherosclerosis in slovenian patients with type 2 diabetes mellitus
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The CHEK2 del5395 is a founder mutation without direct effects for cancer risk in the latvian population
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Detection of mutations in the CYP21A2 gene: genotype-phenotype correlation in Slovenian couples with conceiving problems
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Epigenetic alterations in patients with type 2 diabetes mellitus
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Case Report
A case with Emanuel syndrome: extra derivative 22 chromosome inherited from the mother
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Sarcolemmal deficiency of sarcoglycan complex in an 18-month-old Turkish boy with a large deletion in the beta sarcoglycan gene
, , , oraz
Von Hippel-Lindau disease: the clinical manifestations and genetic analysis results of two cases from a single family
, , , , oraz
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