14 Artikel
Original Article
Uneingeschränkter Zugang | 21. Dez. 2019
Molecular basis of inherited colorectal carcinomas in the Macedonian population: An update
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Uneingeschränkter Zugang | 21. Dez. 2019
Results of liquid biopsy studies by next generation sequencing in patients with advanced stage non-small cell lung cancer: Single center experience from Turkey
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Uneingeschränkter Zugang | 21. Dez. 2019
TWIST1 Gene expression as a biomarker for predicting primary doxorubicin resistance in breast cancer
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Uneingeschränkter Zugang | 21. Dez. 2019
Evaluation of the JAK2V617F mutational burden in patients with philadelphia chromosome negative myeloproliferative neoplasms: A single-center experience
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Uneingeschränkter Zugang | 21. Dez. 2019
Association of variants in the CP , ATOX1 and COMMD1 genes with Wilson disease symptoms in Latvia
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Uneingeschränkter Zugang | 21. Dez. 2019
Association of genetic polymorphisms in the Matrix Gla Protein (MGP) gene with coronary artery disease and serum mgp levels
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Uneingeschränkter Zugang | 21. Dez. 2019
Chronic obstructive pulmonary disease risk and smoking cessation changes induced by CHRNA5-A3 and CHRNB3-A6 variation in a Chinese male population
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Uneingeschränkter Zugang | 21. Dez. 2019
Association of VDR gene variant (rs1544410) with type 2 diabetes in a Pakistani cohort
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Case Report
Uneingeschränkter Zugang | 21. Dez. 2019
Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation
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Uneingeschränkter Zugang | 21. Dez. 2019
Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis
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Uneingeschränkter Zugang | 21. Dez. 2019
Infantile Alexander disease with late onset infantile spasms and hypsarrhythmia
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Uneingeschränkter Zugang | 21. Dez. 2019
Otopalatodigital syndrome type I: novel characteristics and prenatal manifestations in two siblings
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Uneingeschränkter Zugang | 21. Dez. 2019
A Novel splice-site mutation on the MLC1 gene leading to exon 9 skipping and megalencephalic leukoencephalopathy with subcortical cysts in a Turkish patient
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Uneingeschränkter Zugang | 21. Dez. 2019
A 7-year-old boy with hand tremors and a novel mutation for L-2-hydroxyglutaric aciduria
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