Keywords: آرایه CGH; Prenatal array; Chromosomal microarray; Prenatal diagnosis; Array CGH;
مقالات ISI آرایه CGH (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.
Keywords: آرایه CGH; Embryo kinetics; complex abnormalities; array CGH; time lapse;
Keywords: آرایه CGH; Preimplantation genetic diagnosis (PGD); chromosomal rearrangements; array CGH; trophectoderm biopsy; blastocysts;
Keywords: آرایه CGH; Karyotype; Bone marrow stromal cell; Sky; Array CGH;
Keywords: آرایه CGH; Array CGH; chromosomal behavior; live birth; live cell imaging; multinucleation;
Keywords: آرایه CGH; Array CGH; Congenital heart malformations; Copy number variation; Mosaicism
Keywords: آرایه CGH; Endometrial stromal sarcoma; Endometrial stromal nodule; Array CGH;
Keywords: آرایه CGH; MSCs; mesenchymal stem cells; array CGH; array comparative genomic hybridization; FISH; fluorescence in situ hybridization; hAD-MSCs; human adipose tissue-derived mesenchymal stem cells; PBS; phosphate-buffered saline; EDTA; ethylenediaminetetraacetate; Î
Keywords: آرایه CGH; NSCLC; Copy number changes; Array CGH; TP63; Adenocarcinoma; Squamous cell carcinoma
Keywords: آرایه CGH; Array CGH; clonal chromosomal rearrangements; immunoglobulin heavy chain; lymph node hyperplasia; fluorescence in situ hybridization
Keywords: آرایه CGH; Array CGH; genomic instability; pI3 kinase; bioinformatics; tumor suppressor;
Clinical and submicroscopic findings of two prenatal cases with inv dup del(8p) syndrome
Keywords: آرایه CGH; ARHGEF10; Rho guanine nucleotide exchange factor 10; Array CGH; Array comparative genomic hybridization; ASD; Atrial septal defect; CCA; Corpus callosum abnormality; CVA; Cerebellar vermis agenesis; dic(8); Dicentric chromosome 8; FISH; Fluorescence in si
A novel Y chromosome microdeletion potentially associated with defective spermatogenesis identified by custom array comparative genome hybridization
Keywords: آرایه CGH; array CGH; deletion; male infertility; Y chromosome;
Original ArticleGenomic amplification of Fanconi anemia complementation group A (FancA) in head and neck squamous cell carcinoma (HNSCC): Cellular mechanisms of radioresistance and clinical relevance
Keywords: آرایه CGH; Head and neck squamous cell carcinoma; Fanconi anemia; Radiotherapy; Radioresistance; Senescence; DNA damage repair; Array CGH; Microarray-based comparative genomic hybridization; ATM; Ataxia telangiectasia mutated; C12-FDG-FITC; 5-dodecanoylaminofluoresc
Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome
Keywords: آرایه CGH; 2q11.2DS; 22q11.2 deletion syndrome; CNS; central nervous system; CMB; cerebral microbleeds; Array CGH; array - comparative genomic hybridization; EEG; electroencephalography; CT; computed tomography; MRI; magnetic resonance imaging; FFE; fast-field-echo;
Chromosome Xq28 duplication encompassing MECP2: Clinical and molecular analysis of 16 new patients from 10 families in China
Keywords: آرایه CGH; MECP2 duplication; Developmental delay/intellectual disability; Recurrent infections; X chromosome inactivation; Array CGH
Analysis of tissue from products of conception and perinatal losses using QF-PCR and microarray: A three-year retrospective study resulting in an efficient protocol
Keywords: آرایه CGH; Perinatal tissue; Array CGH; QF-PCR; Diagnostic yield
DNA copy number variations are important in the complex genetic architecture of müllerian disorders
Keywords: آرایه CGH; Müllerian; MRKH; CNV; array CGH;
A 1.5Â Mb terminal deletion of 12p associated with autism spectrum disorder
Keywords: آرایه CGH; aCGH; array CGH; ADD; Attention Deficit Disorder; ADHD; Attention Deficit Hyperactivity Disorder; ASD; Autism Spectrum Disorder; B4GALNT3; beta-1,4-N-acetyl-galactosaminyl transferase 3; BAC; bacterial artificial chromosome; CARS; Childhood Autism Rating
Interstitial deletion 1p36.32 in two brothers with a distinct phenotype – Overgrowth, macrocephaly and nearly normal intellectual function
Keywords: آرایه CGH; 1p36 microdeletion; Array CGH; Germline mosaicism
A three-generation family with terminal microdeletion involving 5p15.33–32 due to a whole-arm 5;15 chromosomal translocation with a steady phenotype of atypical cri du chat syndrome
Keywords: آرایه CGH; Cri du chat syndrome; array CGH
Distal 10q monosomy: New evidence for a neurobehavioral condition?
Keywords: آرایه CGH; ADHD; Array CGH; Behavioral troubles; CALY gene; del(10)(q26); Psychiatric disorder
Comprehensive meiotic segregation analysis of a 4-breakpoint t(1;3;6) complex chromosome rearrangement using single sperm array comparative genomic hybridization and FISH
Keywords: آرایه CGH; array CGH; complex chromosome rearrangement; interchromosomal effect; male infertility; meiotic segregation; sperm aneuploidy;
Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism
Keywords: آرایه CGH; Microcephaly; Mental retardation; Array CGH
Short clinical reportMonozygotic twins discordant for 18q21.2qter deletion detected by array CGH in amniotic fluid
Keywords: آرایه CGH; Array CGH; Monozygotic twins; Deletion 18q21.2qter; TCF4 gene;
Neuropathological features in a female fetus with OPHN1 deletion and cerebellar hypoplasia
Keywords: آرایه CGH; OPHN1; Rho-GTPase-activating protein; Cerebellar hypoplasia; Syndromic X-linked mental retardation; Array CGH; Purkinje cells;
Identification of the first deletion-insertion involving the complete structure of GAA gene and part of CCDC40 gene mediated by an Alu element
Keywords: آرایه CGH; MLPA; Multiplex ligation-dependent probe amplification; Array CGH; array-comparative genomic hybridization; PCR; polimerase chain reaction; GAA; glucosidase, alpha, acid; CCDC40; coiled-coil domain containing 40; CDH4; cadherin-4; Kbp; kilobase pairs; GAA
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation
Keywords: آرایه CGH; Limb girdle muscular dystrophy; Array CGH; TRIM32;
Short CommunicationInv21p12q22del21q22 and intellectual disability
Keywords: آرایه CGH; Array CGH; array comparative genomic hybridization; CNVs; copy number variants; DS; Down syndrome; FISH; fluorescence in situ hybridization; ID; intellectual disability; MLPA; multiplex-ligation probe amplification; OMIM; Online Mendelian Inheritance in M
Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridization
Keywords: آرایه CGH; Forensic analysis; Array CGH; Copy number variation; Short tandem repeats;
Combined deletion 18q22.2 and duplication/triplication 18q22.1 causes microcephaly, mental retardation and leukencephalopathy
Keywords: آرایه CGH; 18q deletion syndrome; 18q â syndrome; Array CGH; array comparative genomic hybridization; CNS; central nervous system; CAA; congenital aural atresia; FISH; fluorescence in situ hybridization; UCSC; genome browser hosted by the University of California
De novo 3q22.1 q24 deletion associated with multiple congenital anomalies, growth retardation and intellectual disability
Keywords: آرایه CGH; A4GNT; alpha-1,4-N-acetylglucosaminyltransferase; AGTR1; angiotensin II receptor, type 1; ATR; ataxia telangiectasia and Rad3 related; BAC; bacterial artificial chromosome; BFSP2; beaded filament structural protein 2; BPES; blepharophimosis, ptosis, and e
Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: Phenotypic and genotypic findings
Keywords: آرایه CGH; Array CGH; array comparative genomic hybridization; aCGH; array comparative genomic hybridization; GTG; G banding produced by trypsin and Giemsa; MLPA; multiplex ligation-dependent probe amplification; BMI; body mass index; DMSA; dimercaptosuccinic acid;
Detection of germline rearrangements in patients with α- and β-thalassemia using high resolution array CGH
Keywords: آرایه CGH; α-Thalassemia; β-Thalassemia; δβ-Thalassemia; Hereditary persistence of fetal hemoglobin (HPFH); Array CGH; Multiplex ligation-dependent probe amplification (MLPA); KLF1-gene;
Detailed clinical and molecular study of 20 females with Xq deletions with special reference to menstruation and fertility
Keywords: آرایه CGH; Array CGH; Xq deletion; X;autosome translocation; Premature ovarian failure; X inactivation
24-chromosome copy number analysis: a comparison of available technologies
Keywords: آرایه CGH; Preimplantation genetic screening; aneuploidy; array CGH; quantitative PCR; next generation sequencing
15q11.2 microdeletion and FMR1 premutation in a family with intellectual disabilities and autism
Keywords: آرایه CGH; ID; intellectual delay; PWS; Prader-Willi syndrome; AS; Angelman syndrome; ADHD; attention deficit hyperactivity disorder; ASD; autistic spectrum disorder; array CGH; array-based comparative genomic hybridisation; CNV; copy number variants; 15q11.2 dele
Sequential array comparative genomic hybridization analysis identifies copy number changes during blastic transformation of chronic myeloid leukemia
Keywords: آرایه CGH; Array CGH; Chronic myeloid leukemia; Blastic phase; PAX5; MLLT3
Detection of aneuploidy by array comparative genomic hybridization using cell lines to mimic a mosaic trophectoderm biopsy
Keywords: آرایه CGH; PGS; array CGH; aneuploidy; mosaicism
Molecular cytogenetic characterization of an interstitial deletion of chromosome 21 (21q22.13q22.3) in a patient with dysmorphic features, intellectual disability and severe generalized epilepsy
Keywords: آرایه CGH; Epilepsy; FISH; Array CGH; Chromosomal imbalance; Deletion 21q22; DYRK1; KCNJ6;
Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15.3–p14 and 4.22 Mb in 10q26.3
Keywords: آرایه CGH; 10p15.3–p14 Deletion; 10q26.3 Deletion; Ring chromosome 10; Prenatal diagnosis; Array CGH
BMPR1A is a candidate gene for congenital heart defects associated with the recurrent 10q22q23 deletion syndrome
Keywords: آرایه CGH; BMPR1A; Congenital heart defects; 10q22q23; Gene prioritization; AVSD; Array CGH
Hypoperfusion in caudate nuclei in patients with brain-lung-thyroid syndrome
Keywords: آرایه CGH; Brain-lung-thyroid syndrome; NKX2-1; Array CGH; ECD-SPECT; eZIS;
Prenatal diagnosis of a 12q22q23.2 interstitial deletion by array CGH in a malformed fetus
Keywords: آرایه CGH; Array CGH; Microdeletion; IGF1 gene; Prenatal diagnosis
Small supernumerary marker chromosomes derived from chromosomes 6 and 20 in a woman with recurrent spontaneous abortions
Keywords: آرایه CGH; Small supernumerary marker chromosomes (sSMC); Array CGH; FISH; Recurrent abortions
Acquired genomic copy number changes in CML patients with the Philadelphia chromosome (Ph+)
Keywords: آرایه CGH; CML; array CGH; Philadelphia chromosome; BCR; ABL1;
Interstitial deletion of chromosome 2p15-16.1: Report of two patients and critical review of current genotype–phenotype correlation
Keywords: آرایه CGH; Array CGH; Developmental delay; Dysmorphic features; Microdeletion 2p15p16.1 syndrome
Array CGH and PIK3CA/AKT1 mutations to drive patients to specific targeted agents: A clinical experience in 108 patients with metastatic breast cancer
Keywords: آرایه CGH; AKT1; Array CGH; Breast cancer; PIK3CA; Targeted therapy;
A novel 506 kb deletion causing εγδβ thalassemia
Keywords: آرایه CGH; εγδβ thalassemia; Palindrome; Array CGH; MLPA (Multiplex Ligation-dependent Probe Amplification)
De novo microdeletions of chromosome 6q14.1-q14.3 and 6q12.1-q14.1 in two patients with intellectual disability - further delineation of the 6q14 microdeletion syndrome and review of the literature
Keywords: آرایه CGH; 6q14 microdeletion syndrome; Intellectual disability; Mental retardation; Array CGH