Keywords: کروموزوم 7; MET; MET proto-oncogene, receptor tyrosine kinase; FISH; fluorescence in situ hybridization; EGFR; epidermal growth factor receptor; PCR; polymerase chain reaction; TCGA; The Cancer Genome Atlas; VEGF; vascular endothelial growth factor; CEP7; chromosome
مقالات ISI کروموزوم 7 (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Molecular approaches identify a cryptic MECOM rearrangement in a child with a rapidly progressive myeloid neoplasm
Keywords: کروموزوم 7; Molecular cytogenetics; myeloid neoplasm; MECOM gene; array-CGH; RTqPCR; chromosome 7; cryptic abnormalities;
Chromosome 7q31.1 deletion in myeloid neoplasms
Keywords: کروموزوم 7; DNA; Deletion; Chromosome 7; Myeloid neoplasms; Single nucleotide polymorphism
Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: Does −7/7q− detection by FISH have prognostic value?
Keywords: کروموزوم 7; MDS; Cytogenetics; FISH; Chromosome 7
Autistic regression in a child with Silver–Russell Syndrome and maternal UPD 7
Keywords: کروموزوم 7; UPD 7; UPD; Chromosome 7; Silver–Russell syndrome; Autism
Single nucleotide polymorphism array-based karyotyping shows sequential genomic changes from monosomy to copy-neutral loss of heterozygosity of chromosome 7 and 20q deletion within a balanced translocation t(14;20) in AML
Keywords: کروموزوم 7; Chromosome 7; monosomy; copy-neutral LOH; clonal evolution
Interstitial deletion of 7q31.32 → q33 secondary to a paracentric inversion of a maternal chromosome 7
Keywords: کروموزوم 7; Chromosome 7; Paracentric inversion; Recombinants; Deletion 7q; Array-CGH
Sonic Hedgehog deletion and distal trisomy 3p in a patient with microphthalmia and microcephaly, lacking cerebral anomalies typical of holoprosencephaly
Keywords: کروموزوم 7; Chromosome 7; Chromosome 3; Holoprosencephaly; Microphthalmia; SHH
Epigenetics in Silver-Russell syndrome
Keywords: کروموزوم 7; Silver-Russell syndrome; genomic imprinting; uniparental disomy; chromosome 11p15 region; chromosome 7
Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: A case-control study
Keywords: کروموزوم 7; Autistic disorder; Chromosome 7; TAC1; Genetic association; Glutamate system; Haplotype block
HIC gene, a candidate suppressor gene within a minimal region of loss at 7q31.1 in myeloid neoplasms
Keywords: کروموزوم 7; Acute myeloid leukemia; Myelodysplasia; DNA; Deletion; Chromosome 7; Human I-mfa domain-containing protein; MDFIC
Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22
Keywords: کروموزوم 7; Chromosome 7; Acute myeloid leukemia; Myelodysplastic syndrome; Monosomy 7; F-box proteins;