Search Results - "microarray analysis"
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1
Evaluation of Genomic Variants in Non-syndromic Congenital Heart Disease in Turkish Pediatric Group
Published 2025-07-01Subjects: Get full text
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Phenomenon of loss of heterozygosity in tumour tissue of breast cancer: association with expression of monoresistance genes
Published 2018-01-01Subjects: Get full text
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Aberrations of the number of copies (CNA) in the genome of luminal B breast tumor
Published 2020-10-01Subjects: Get full text
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A Clinical and Molecular Description of a Rare Case of Chromosomal Abnormality (Partial Trisomy 14q11.2-q21.1 and Partial Monosomy 21q11.2-q21.3)
Published 2016-08-01Subjects: Get full text
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5
The use of chromosomal microarray analysis for diagnostics of chromosomal pathology in fetal central nervous system malformations
Published 2020-10-01Subjects: “…chromosomal microarray analysis…”
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Search for polymorphic variants of candidate genes contributing to individual radiosensitivity
Published 2023-01-01Subjects: Get full text
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7
MICROARRAY ANALYSIS OF DNA COPY NUMBER ABERRATION IN BREAST TUMOR: CORRELATION WITH THE EFFICACY OF NEOADJUVANT CHEMOTHERAPY
Published 2016-02-01Subjects: Get full text
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Role of transcriptomics in the study of oral cancer
Published 2025-07-01Subjects: Get full text
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9
Application of chromosome microarray analysis and karyotyping in fetal cardiac abnormalities
Published 2025-06-01Subjects: “…chromosome microarray analysis…”
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10
RESPONSE TO NEOADYAVANT CHEMOTHERAPY WITH PLATINUM-BASED DRUGS IN BREAST CANCER PATIENTS WITH BRCA1 DELETION IN TUMOR
Published 2019-06-01Subjects: Get full text
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Analysis of potential genes and pathways associated with the colorectal normal mucosa–adenoma–carcinoma sequence
Published 2018-06-01Subjects: Get full text
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12
LOSS OF HETEROZYGOSITY IN THE BRCA1 AND BRCA2 LOCUS IN BREAST CANCER
Published 2020-07-01Subjects: Get full text
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Xq12q13.2 duplication detected in a child in selective exome screening
Published 2024-09-01Subjects: Get full text
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Identification of a novel microdeletion at 9q21.13 in a family with epilepsy, intellectual disability, and speech disorders and literature review
Published 2025-07-01Subjects: Get full text
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HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES
Published 2016-08-01Subjects: Get full text
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