Keywords: کاریتیپینگ; Acute Lymphoblastic Leukemia; Cytogenetics; Karyotyping; Bone marrow culture;
مقالات ISI ترجمه شده کاریتیپینگ
مقالات ISI کاریتیپینگ (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: کاریتیپینگ; Genetics; Infertility; Azoospermia; Karyotyping; Oligozoospermia;
Keywords: کاریتیپینگ; Global developmental delay (GDD); Dysmorphic features; Karyotyping; Down syndrome; Structural chromosomal abnormalities;
Keywords: کاریتیپینگ; RC; ring chromosome; AML; acute myeloid leukemia; MDS; myelodysplastic syndrome; AML-RC; acute myeloid leukemia with ring chromosome; MDS-RC; myelodysplastic syndrome with ring chromosome; AML-N; acute myeloid leukemia without ring chromosome; MDS-N; myel
Keywords: کاریتیپینگ; copy number variation; karyotyping; products of conception; single nucleotide polymorphism array; uniparental disomy
Keywords: کاریتیپینگ; Primary and secondary amenorrhea; Karyotyping; Chromosomal abnormalities
Keywords: کاریتیپینگ; Chromosomes; Centromere; Karyotyping; Homologue chromosome; Genetic disorder;
Detection of fetal trisomy 9 mosaicism by noninvasive prenatal testing through maternal plasma DNA sequencing
Keywords: کاریتیپینگ; Amniocentesis; Karyotyping; Maternal plasma DNA; Noninvasive prenatal testing; Trisomy 9 mosaicism;
Research paperEstablishment of cell line with NK/NKT phenotype from myeloid NK cell acute leukemia
Keywords: کاریتیپینگ; Acute myeloid leukemia (AML); Cell line; Karyotyping; NK/NKT phenotype; Cytoxicity;
Towards an autonomous human chromosome classification system using Competitive Support Vector Machines Teams (CSVMT)
Keywords: کاریتیپینگ; Support Vector Machines; Karyotyping; Chromosome classification; Committee machines;
Prenatal diagnosis of paternal duplication of 11p15.5â14.3: Its implication of Beckwith-Wiedemann syndrome
Keywords: کاریتیپینگ; array comparative genomic hybridization; Beckwith-Wiedemann syndrome; karyotyping; short tandem repeat marker;
ARHGAP4 mutated in a Chinese intellectually challenged family
Keywords: کاریتیپینگ; XLMR; X-linked mental retardation; EEG; Electroencephalogram; MRI; Magnetic resonance imaging; PHA; Phytohemagglutinin; LM-PCR; Ligation-mediated polymerase chain reaction; SNPs; Single nucleotide polymorphisms; InDels; Insertions or deletions; BWA; Burro
Karyotyping and identifying all of the chromosomes of allopolyploid Brassica juncea using multicolor FISH
Keywords: کاریتیپینگ; Brassica juncea; Karyotyping; Fluorescence in situ hybridization; Repetitive DNA sequence
Amplification-free sequencing of cell-free DNA for prenatal non-invasive diagnosis of chromosomal aberrations
Keywords: کاریتیپینگ; Amplification-free; Library preparation; Cell-free DNA; Karyotyping; Bias; Fetal aneuploidy
Sequential combination of karyotyping and RNA-sequencing in the search for cancer-specific fusion genes
Keywords: کاریتیپینگ; FISH; fluorescence in situ hybridization; NGS; next generation sequencing; RNA-Seq; RNA sequencing; WES; whole exome sequencing; WGS; whole genome sequencing; Karyotyping; RNA-sequencing; Cancer-specific fusion genes;
Production of female bovine embryos with sex-sorted sperm using intracytoplasmic sperm injection: Efficiency and in vitro developmental competence
Keywords: کاریتیپینگ; Bovine; Embryo development rate; Intracytoplasmic sperm injection; In vitro fertilization; Karyotyping; Sex-sorted sperm;
Tetraploidy in the era of molecular karyotyping - What we need to remember
Keywords: کاریتیپینگ; Tetraploidy; Newborn; Karyotyping;
Cardiac anomalies in individuals with the 18q deletion syndrome; report of a child with Ebstein anomaly and review of the literature
Keywords: کاریتیپینگ; 18q Deletion syndrome; Genotype-phenotype correlation; Congenital heart defects; Ebstein anomaly; Microarray; Karyotyping;
Cytogenetic studies in children with learning disability
Keywords: کاریتیپینگ; Learning disability; Karyotyping; Fragile-X syndrome; FMR-1 gene;
Cytogenetic Evaluation: A Primer for Pediatric Nurse Practitioners
Keywords: کاریتیپینگ; Cytogenetics; karyotyping; FISH; CGH; chromosomal microarrays
The evolving electroclinical syndrome of “epilepsy with ring chromosome 20”
Keywords: کاریتیپینگ; Ring chromosome 20; Refractory epilepsy; Karyotyping;
Handmade cloned and parthenogenetic goat embryos - A comparison of different culture media and donor cells
Keywords: کاریتیپینگ; Goat; Manual cloning; Karyotyping; Parthenogenesis; PCR; Protrusion cone;
Genomic imbalances in endometrial adenocarcinomas – Comparison of DNA ploidy, karyotyping and comparative genomic hybridization
Keywords: کاریتیپینگ; DNA ploidy; Comparative genomic hybridization; Karyotyping; Endometrial adenocarcinoma; Endometrioid; AneuploidyEndometrial adenocarcinoma, EAC; comparative genomic hybridization, CGH; average number of copy alterations, ANCA
A review of thresholding strategies applied to human chromosome segmentation
Keywords: کاریتیپینگ; Chromosome analysis; Karyotyping; Image segmentation; Level set; Thresholding; Particle swarm
Chromosomal aberrations in 2000 couples of Indian ethnicity with reproductive failure
Keywords: کاریتیپینگ; chromosomal aberrations; genetic counselling; infertility; karyotyping; recurrent spontaneous abortions; reproductive failure
Karyotyping, Is It Worthwhile in Transsexualism?
Keywords: کاریتیپینگ; Karyotyping; Transsexualism; Prevalence; Chromosomal Abnormalities; Klinefelter Syndrome; Disorders of Sexual Differentiation;
Multiple chromosomal monosomies are characteristic of giant cell ependymoma
Keywords: کاریتیپینگ; Giant cell ependymoma; Anaplastic ependymoma; Karyotyping; Aneuploidy; DNA ploidy analysis; Array comparative genomic hybridization
Genome size, karyotyping and FISH physical mapping of 45S and 5S genes in two cherry rootstocks: Prunus subhirtella and Prunus incisa × serrula
Keywords: کاریتیپینگ; Prunus; Double-colour FISH; Repetitive DNA; Chromosome identification; Karyotyping
A comprehensive cytogenetics tutorial program, encompassing changeable G-band resolutions
Keywords: کاریتیپینگ; Chromosome; Karyotyping; G-band resolutions; Virtual reality
Identifying touching and overlapping chromosomes using the watershed transform and gradient paths
Keywords: کاریتیپینگ; Chromosome classification; Watershed transform; Karyotyping; Multiplex Fluorescent In Situ Hybridization
t(3;21)(q22;q22) leading to truncation of the RYK gene in atypical chronic myeloid leukemia
Keywords: کاریتیپینگ; Fusion gene; Karyotyping; RYK; ATP5O; aCML
Revised karyotyping and gene mapping of the Biomphalaria glabrata embryonic (Bge) cell line
Keywords: کاریتیپینگ; Biomphalaria glabrata; Schistosomiasis; Chromosomes; Karyotyping; Bge cell line; Fluorescence in situ hybridization (FISH); Bacterial artificial chromosomes (BACs); Mapping
Array analysis and karyotyping: Workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands
Keywords: کاریتیپینگ; Idiopathic developmental delay; Mental retardation; Karyotyping; Array-based genome investigation; Array-CGH
Low erythropoietin production as non-oncogenic co-factor contributing to disease-manifestation in low-risk MDS: A hypothesis supported by unique case reports
Keywords: کاریتیپینگ; Diagnostic criteria; MDS; Karyotyping; ICUS; Erythropoietin
SKY reveals a high frequency of unbalanced translocations involving chromosome 6 in t(12;21)-positive acute lymphoblastic leukemia
Keywords: کاریتیپینگ; Acute lymphoblastic leukemia; Karyotyping; SKY; Child
Single umbilical artery in fetopathological investigations
Keywords: کاریتیپینگ; Single umbilical artery (SUA); Fetopathological examination; Associated malformations; Chromosome aberration; Karyotyping
Ãvaluation de l'amniocentèse au troisième trimestre pour le dépistage des anomalies chromosomiques chez les patientes n'acceptant pas le risque de perte fÅtale
Keywords: کاریتیپینگ; Amniocentèse; Caryotype; Rupture prématurée des membranes; Accouchement prématuré; Chorioamniotite; Amniocentesis; Third trimester; Karyotyping; Fetal loss; Preterm premature rupture of membranes; Preterm birth; Chorioamniotitis; FISH;
Ãvaluation de l'amniocentèse au troisième trimestre pour le dépistage des anomalies chromosomiques chez les patientes n'acceptant pas le risque de perte fÅtale
Keywords: کاریتیپینگ; Amniocentèse; Caryotype; Rupture prématurée des membranes; Accouchement prématuré; Chorioamniotite; Amniocentesis; Third trimester; Karyotyping; Fetal loss; Preterm premature rupture of membranes; Preterm birth; Chorioamniotitis; FISH;
A rule-based computer scheme for centromere identification and polarity assignment of metaphase chromosomes
Keywords: کاریتیپینگ; Human chromosomes; Karyotyping; Fully medial axis finding; Centromere identification; Polarity assignment
Automatic segmentation of metaphase cells based on global context and variant analysis
Keywords: کاریتیپینگ; Automatic chromosome segmentation; Karyotyping; Shape analysis; Context; Variant analysis; Diagnostic classification
Synovial sarcoma of the larynx in a 79-year-old woman, confirmed by karyotyping and fluorescence in situ hybridization analysis
Keywords: کاریتیپینگ; Synovial sarcoma; Larynx; Immunohistochemistry; Karyotyping; FISH
Idiopathic cytopenia of undetermined significance (ICUS) versus low risk MDS: The diagnostic interface
Keywords: کاریتیپینگ; Myelodysplastic syndromes; Minimal criteria; Karyotyping; FISH
Conventional and molecular cytogenetic diagnostic methods in stem cell research: A concise review
Keywords: کاریتیپینگ; Stem cell research; Cytogenetics; Fluorescence in situ hybridization; Karyotyping; Comparative genomic hybridization; Spectral karyotyping;
Ewing sarcoma/primitive neuroectodermal tumor of the kidney: a case report. Diagnosed by immunohistochemistry and molecular analysis
Keywords: کاریتیپینگ; Ewing sarcoma; Primitive neuroectodermal tumor; Immunohistochemistry; Karyotyping; FISH
Efficacy and safety of cordocentesis for prenatal diagnosis
Keywords: کاریتیپینگ; β-Thalassemia; Complications; Cordocentesis; Karyotyping; Prenatal diagnosis
Candida albicans isolates with different genomic backgrounds display a differential response to macrophage infection
Keywords: کاریتیپینگ; Candida albicans; Karyotyping; Macrophage infection; SAP1–10 gene expression; Morphogenesis
Fausses couches spontanées précoces répétées : quelle prise en charge proposer en 2006 ?
Keywords: کاریتیپینگ; Fausses couches; Avortement; Anticardiolipides; Caryotype; Thrombophilie; Cloison utérine; Biais d'inactivation de l'XMiscarriage; Abortion; Recurrent pregnancy loss; Anticardiolipin; Karyotyping; Thrombophilia; Septate uterus; Skewed-X-chromosome inactiv
Electrophoresis karyotype and chromosome-length polymorphism of Histoplasma capsulatum clinical isolates from Latin America
Keywords: کاریتیپینگ; Histoplasma capsulatum; Karyotyping; Pulsed-field gel electrophoresis; Chromosomes;
Multiple numerical chromosome aberrations in cancer: what are their causes and what are their consequences?
Keywords: کاریتیپینگ; Karyotyping; Numerical chromosome changes; Aneuploidy; Chromosome instability; Clonal evolution;
Supervised parametric and non-parametric classification of chromosome images
Keywords: کاریتیپینگ; M-FISH; Nearest neighbor; k-nearest neighbor; Maximum likelihood estimation; Karyotyping;