Keywords: قاضی; Prostate cancer; Genomic classifier; Decipher; Detectable PSA; Persistent PSA; Prostatectomy; Biomarker; PSA;
مقالات ISI قاضی (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: قاضی; Autism spectrum disorder; Chromosome microarray analysis; Diagnostic yield; Global developmental delay; SNP microarray; DSM-5; Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition; ID; Intellectual Disability; ISCA; International Standards
Whole exome sequencing identifies a novel 5â¯Mb deletion at 14q12 region in a patient with global developmental delay, microcephaly and seizures
Keywords: قاضی; RTT; Rett syndrome; MECP2; Methyl-CpG-Binding Protein 2; CDKL5; Cyclin Dependent Kinase Like 5; FOXG1; Forkhead Box G1; OMIM; Online Mendelian Inheritance in Man; PRKD1; Protein Kinase D1; NOVA1; Neurooncologic Ventral Antigen 1; c14orf23; Chromosome 14 O
Comparison of SHOX and associated elements duplications distribution between patients (LÄri-Weill dyschondrosteosis/idiopathic short stature) and population sample
Keywords: قاضی; ASMT; acetylserotonin O-methyltransferase; CNE; conserved non-coding elements; CNV; copy number variant; DECIPHER; Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources; DGV; Database of Genomic Variants; ISS; idiopathic short
Identification of a patient with intellectual disability and de novo 3.7Â Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15
Keywords: قاضی; Mb; megabase; SNP; single nucleotide polymorphism; ID; intellectual disability; HC; head circumference; SD; standard deviation; MRI; magnetic resonance imaging; FMR1; fragile X mental retardation 1; PCR; polymerase chain reaction; FISH; fluorescence in si
Monosomy 9pter and trisomy 9q34.11qter in two sisters due to a maternal pericentric inversion
Keywords: قاضی; CEBIOR; Center for Biomedical Research; CNAG; Copy Number Analyzer for Affymetrix Genechip mapping; DECIPHER; Database of chromosomal imbalance and phenotype in humans using Ensembl Resources; DGHE; Directorate of Higher Education; DGV; Database of Genomi
Cytogenomic characterization of an unexpected 17.6 Mb 9p deletion associated to a 14.8 Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype
Keywords: قاضی; MLPA; multiplex-ligation probe amplification; FISH; Fluorescence in situ hybridization; OFC; Occipital-frontal circumference; MRI; Magnetic resonance imaging; DECIPHER; Database of Chromosomal Imbalance and Phenotype in Humans using Ensembl Resources; O
A post-detection decipherment strategy
Keywords: قاضی; Post-detection; Decipher; Strategy