10 Artikel
Uneingeschränkter Zugang | 08. Dez. 2011
Evidence for Correlation of Fragile Sites and Chromosomal Breakpoints in Carriers of Constitutional Balanced Chromosomal Rearrangements
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Uneingeschränkter Zugang | 08. Dez. 2011
Hypergonadotropic Hypogonadism, Progressive Early-Onset Spinocerebellar Ataxia, and Late-Onset Sensorineural Hearing Loss: Case Report and Literature Review
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Uneingeschränkter Zugang | 08. Dez. 2011
Diagnosis of Fanconi's Anemia by Diepoxybutane Analysis in Children from Serbia
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Uneingeschränkter Zugang | 08. Dez. 2011
Amplification of c-MYC and MLL Genes as a Marker of Clonal Cell Progression in Patients with Myeloid Malignancy and Trisomy of Chromosomes 8 or 11
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Uneingeschränkter Zugang | 08. Dez. 2011
Molecular Analysis of Ring Y Chromosome in a 10-Year-Old Boy with Mixed Gonadal Dysgenesis and Growth Hormone Deficiency
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Uneingeschränkter Zugang | 08. Dez. 2011
Metadata Management and Semantics in Microarray Repositories
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Uneingeschränkter Zugang | 08. Dez. 2011
IL-18 Gene Promoter Region 607C/A Polymorphism in HIV-1 Infected North Indian Population
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Uneingeschränkter Zugang | 08. Dez. 2011
Alterations of Copy Number of Methylation Pattern in Mismatch Repair Genes by Methylation Specific-Multiplex Ligation-Dependent Probe Amplification in Cases of Colon Cancer
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Uneingeschränkter Zugang | 08. Dez. 2011
Role of the APOB Gene Polymorphism (c.12669G>A, p. Gln4154Lys) in Coronary Artery Disease in the Indian Punjabi Population
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