
10 Artykułów
Frequencies of Single-Nucleotide Polymorphisms and Haplotypes of the SLCO1B1 Gene in Selected Populations of the Western Balkans
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Prevalence of Chromosomal Abnormalities in Infertile Couples in Romania
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Investigation of Fasciculation and Elongation Protein ζ-1 (FEZ1) in Peripheral Blood Reveals Differences in Gene Expression in Patients with Schizophrenia
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The Relationship Between Transcript Expression Levels of Nuclear Encoded (TFAM, NRF1) and Mitochondrial Encoded (MT-CO1) Genes in Single Human Oocytes During Oocyte Maturation
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Clinical Relevance of CHEK2 And NBN Mutations in the Macedonian Population
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KIR And HLA Haplotype Analysis in a Family Lacking The KIR 2DL1-2DP1 Genes
oraz
Three Novel Mutations of CHD7 Gene in Two Turkish Patients with Charge Syndrome; A Double Point Mutation and an Insertion
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Early Onset Marfan Syndrome: Atypical Clinical Presentation of Two Cases
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Congenital Hydrocephalus and Hemivertebrae Associated With De NOVO Partial Monosomy 6q (6q25.3→qter)
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Report of a New Case With Pentasomy X and Novel Clinical Findings
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