14 Artikel
Original Article
Uneingeschränkter Zugang | 02. Aug. 2016
Gene mapping in an anophthalmic pedigree of a consanguineous Pakistani family opened new horizons for research
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Uneingeschränkter Zugang | 02. Aug. 2016
Investigation of the N-terminal coding region of MUC7 alterations in dentistry students with and without caries
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Uneingeschränkter Zugang | 02. Aug. 2016
PECAM-1 gene polymorphism (rs668) and subclinical markers of carotid atherosclerosis in patients with type 2 diabetes mellitus
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Uneingeschränkter Zugang | 02. Aug. 2016
Association of the MTHFR C677T (rs1801133) polymorphism with idiopathic male infertility in a local Pakistani population
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Uneingeschränkter Zugang | 02. Aug. 2016
Frequency and association of 1691 (G>A) FVL, 20210 (G>A) PT and 677 (C>T) MTHFR with deep vein thrombosis in the population of Bosnia and Herzegovina
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Uneingeschränkter Zugang | 02. Aug. 2016
Genetic and clinical analysis of nonsyndromic hearing impairment in pediatric and adult cases
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Uneingeschränkter Zugang | 02. Aug. 2016
Prevalence and mutations of β-thalassemia trait and abnormal hemoglobins in premarital screening in Çanakkale province, Turkey
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Uneingeschränkter Zugang | 02. Aug. 2016
The influence of CYP2C8*3 on carbamazepine serum concentration in epileptic pediatric patients
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Uneingeschränkter Zugang | 02. Aug. 2016
Assessment of genotoxicity of vincristine, vinblastine and vinorelbine in human cultured lymphocytes: a comparative study
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Uneingeschränkter Zugang | 02. Aug. 2016
Embryo quality predictive models based on cumulus cells gene expression
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Case Report
Uneingeschränkter Zugang | 02. Aug. 2016
Recurrent increased nuchal translucency: a first trimester presentation of familial 13p satellite deletion
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Uneingeschränkter Zugang | 02. Aug. 2016
Von recklinghausen disease: one patient – various problems
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Uneingeschränkter Zugang | 02. Aug. 2016
T-lymphoblastic leukemia/lymphoma in macedonian patients with Nijmegen breakage syndrome
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Uneingeschränkter Zugang | 02. Aug. 2016
Neuroradiological, neurophysiological and molecular findings in infantile Krabbe disease: two case reports
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