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You searched for: Author/Creator Krepischi, Ana C. V.

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1. Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. Issue 8 (14th May 2021)

2. Cytogenetically visible inversions are formed by multiple molecular mechanisms. Issue 11 (1st October 2020)

3. Detection of mosaicism for segmental and whole chromosome imbalances by targeted sequencing. (6th August 2020)

4. Differential DNA Methylation of MicroRNA Genes in Temporal Cortex from Alzheimer's Disease Individuals. (26th April 2016)

5. DNA Methylation Levels of Melanoma Risk Genes Are Associated with Clinical Characteristics of Melanoma Patients. (12th April 2015)

6. Genotype‐phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literature. Issue 3 (7th December 2015)