Keywords: غربالگری ژنتیکی; Muscular Disorders, Atrophic; Receptors, Androgen; Gynaecomastia; Sexual dysfunction; Genetic screening; Genes; Genetic diseases, X-linked;
مقالات ISI غربالگری ژنتیکی (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: غربالگری ژنتیکی; Fabry disease; Genetic screening; High resolution melting analysis;
Keywords: غربالگری ژنتیکی; genetic screening; hemoglobin Bart's; hemoglobinopathy; CBC; Complete blood count; Hb H; Hemoglobin H; NBS; Newborn screening;
Keywords: غربالگری ژنتیکی; Functional assay; Genetic screening; Lipase maturation factor-1 (LMF1); LPL activity; Pathogenicity evaluation; Severe hypertriglyceridemia;
Keywords: غربالگری ژنتیکی; Fabry disease; cryptogenic stroke; X-linked; genetic screening;
Keywords: غربالگری ژنتیکی; Aneuploidy; Genetic screening; Noninvasive prenatal screening; Cell-free DNA; Chorionic villus sampling; Amniocentesis;
Keywords: غربالگری ژنتیکی; Mendelian; genetic screening; carrier screening;
Keywords: غربالگری ژنتیکی; Congenital hypothyroidism; Thyroglobulin gene; Genetic screening; Variants interpretationTG, thyroglobulin; CH, congenital hypothyroidism; PCH, permanent congenital hypothyroidism; VUS, variants of unknown significance; ACHE, acetylcholinesterase; TSH, th
Keywords: غربالگری ژنتیکی; Spinal muscular atrophy; Genetic screening; Therapy;
Keywords: غربالگری ژنتیکی; Prenatal screening; Aneuploidy screening; Genetic screening;
Keywords: غربالگری ژنتیکی; Psoriatic arthritis; Psoriasis; Biomarkers; Genetic screening;
Keywords: غربالگری ژنتیکی; Familial hypercholesterolemia registry; Cardiovascular diseases; Cascade testing; Mutations; Genetic screening;
Keywords: غربالگری ژنتیکی; Assisted reproductive technology; carrier; genetic screening; infertility; next-generation sequencing
Keywords: غربالگری ژنتیکی; UK; Fatherhood; Antenatal care; Genetic screening; Sickle cell; Masculinity;
Keywords: غربالگری ژنتیکی; Newborn screening; Genetic screening; Ethics; Public policy; Duchenne muscular dystrophy; Krabbe disease; Fragile X syndrome;
Keywords: غربالگری ژنتیکی; Genetic screening; genetic test; biomarker; single nucleotide polymorphism; personalized medicine; tooth extraction; tooth loss; preventive care; clinical data reanalysis; ASW; African Americans from the Southwest; CEU; Caucasians from Utah; CHB; Han Chin
Keywords: غربالگری ژنتیکی; Madelung's deformity; Children; Genetic screening; Léri-Weill syndrome; Turner syndrome
Keywords: غربالگری ژنتیکی; Carrier screening; Cystic fibrosis carrier screening; Genetic screening; Population screening; Attitudes;
Keywords: غربالگری ژنتیکی; Ashkenazi Jewish; genetic screening; genomic medicine; preconception care; prenatal testing;
Keywords: غربالگری ژنتیکی; Genetic dynamics; Genetic screening; Optimal control;
Keywords: غربالگری ژنتیکی; alcohol septal ablation; genetic screening; hypertrophic cardiomyopathy; implantable cardioverter-defibrillators; sudden cardiac death; surgical myectomy
Keywords: غربالگری ژنتیکی; Semen donor; sperm donor; genetic screening; informed consent;
Maturity Onset Diabetes of the Young (MODY) in Tunisia: Low frequencies of GCK and HNF1A mutations
Keywords: غربالگری ژنتیکی; Apo A; apolipoprotein A; Apo B; apolipoprotein B; BMI; body mass index; DHPLC; Denaturing High Performance Liquid Chromatography; GAD; Anti-Glutamic acid Decarboxylase; HbA1c; glycated hemoglobin; HDL-C; high-density lipoprotein cholesterol; HLA-DRB1; HLA
Beyond ALS and FTD: the phenotypic spectrum of TBK1 mutations includes PSP-like and cerebellar phenotypes
Keywords: غربالگری ژنتیکی; TBK1; PSP; Ataxia; Whole-exome sequencing; Genetic screening; FTD;
Beyond BRCA: A Case Series Examining the Advent of Multigene Panel Testing
Keywords: غربالگری ژنتیکی; ATM; BRIP1; Carcinogenic risk; CHEK2; Genetic screening; Hereditary; Ovarian cancer; PTEN; RAD50; Variant of uncertain significance;
A multiplex ARMS PCR approach to detection of common β-globin gene mutations
Keywords: غربالگری ژنتیکی; ARMS PCR; Ã-thalessamia; Multiplex PCR; Genetic screening; MARMS;
Unrecognized Fibrinogen A α-Chain Amyloidosis: Results From Targeted Genetic Testing
Keywords: غربالگری ژنتیکی; Amyloidosis; chronic kidney disease (CKD); fibrinogen A alpha-chain; genetic screening; hemodialysis; mutation; proteinuria; hypertension; FGA p.Glu545Val; Portugal; end-stage renal disease (ESRD);
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases
Keywords: غربالگری ژنتیکی; Genotyping; NeuroX; NeuroChip; Genetic screening; Neurodegeneration;
Cell-free DNA screening in clinical practice: abnormal autosomal aneuploidy and microdeletion results
Keywords: غربالگری ژنتیکی; aneuploidy; cell-free DNA; genetic screening; microdeletion; noninvasive prenatal testing; prenatal diagnosis; positive predictive value; trisomy 13; trisomy 18; trisomy 21;
Next-generation sequencing of 28 ALS-related genes in a Japanese ALS cohort
Keywords: غربالگری ژنتیکی; Amyotrophic lateral sclerosis; Japan; Genetic screening; Next-generation sequencer;
Adaptability of sunflower (Helianthus annuus L.) high oleic hybrids to different Italian areas for biodiesel production
Keywords: غربالگری ژنتیکی; Sunflower crop; High oleic genotype; Climatic conditions; Genetic screening; Biofuel
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants
Keywords: غربالگری ژنتیکی; ALS; FTD; SOD1; FUS; C9ORF72; TARDBP; Genetic screening;
An effective enrichment strategy for EML4-ALK fusion gene screening in patients with non-small cell lung cancer
Keywords: غربالگری ژنتیکی; EML4-ALK fusion gene; Non-small cell lung cancer; Genetic screening; Driver gene mutation;
Newborn hearing concurrent genetic screening for hearing impairment-A clinical practice in 58,397 neonates in Tianjin, China
Keywords: غربالگری ژنتیکی; GJB2; GJB3; SLC26A4; MTRNR1; Newborn hearing screening; Genetic screening;
A reverse dot blot assay for the expanded screening of eleven Chinese G6PD mutations
Keywords: غربالگری ژنتیکی; Glucose 6-phosphate dehydrogenase deficiency (G6PD); Reverse dot blot (RDB); Multiplex polymerase reaction (M-PCR); Point mutation; Genetic screening
Genetics and Preterm Birth
Keywords: غربالگری ژنتیکی; preterm birth; premature birth; genetic screening; parturition; SNPs; GWAS; NGS;
Emotional and Psychological Implications of Early AD Diagnosis
Keywords: غربالگری ژنتیکی; Emotion; Psychology; Early diagnosis; Alzheimer disease; Early-onset dementia; Genetic screening; Caregiver; Diagnosis disclosure;
Offering antenatal sickle cell and thalassaemia screening in primary care: A pre-post evaluation of a brief type of communication skills training
Keywords: غربالگری ژنتیکی; Evaluation; Primary health care; Genetic screening; Thalassaemia; Sickle cell; Antenatal diagnosis;
Factors influencing intention to undergo whole genome screening in future healthcare: A single-blind parallel-group randomised trial
Keywords: غربالگری ژنتیکی; Screening; Genome; Genetic screening; Sequence analysis; DNA; Individualised medicine; Psychological models; Information disclosure; Consumer information handout;
COMBINATORIAL APPROACHES FOR INVERSE METABOLIC ENGINEERING APPLICATIONS
Keywords: غربالگری ژنتیکی; inverse metabolic engineering; genetic engineering; microbes; genetic screening; mutagenesis
Cardiovascular Disease in India
Keywords: غربالگری ژنتیکی; Cardiovascular diseases; Young Indians; Risk factors; Biomarkers; Genetic screening;
Genetic Screening and Counseling: Family Medicine Obstetrics
Keywords: غربالگری ژنتیکی; Genetic screening; Family medicine; Obstetrics; Genetic counseling;
Newborn screening and maternal diagnosis: Rethinking family benefit
Keywords: غربالگری ژنتیکی; USA; Newborn screening; Genetic screening; Genetic technologies; Health and families; Maternal health; Benefit
PICOGEN: experiencia de 5 años de un programa de asesoramiento genético en demencia
Keywords: غربالگری ژنتیکی; Consejo genético; Pruebas genéticas; Demencia familiar; Enfermedad de Alzheimer; Degeneración lobular frontotemporal; Enfermedades priónicas; Genetic counselling; Genetic screening; Familial dementia; Alzheimer disease; Frontotemporal lobar degenerati
PICOGEN: Five years experience with a genetic counselling program for dementia
Keywords: غربالگری ژنتیکی; Genetic counselling; Genetic screening; Familial dementia; Alzheimer disease; Frontotemporal lobar degeneration; Prion diseasesConsejo genético; Pruebas genéticas; Demencia familiar; Enfermedad de Alzheimer; Degeneración lobular frontotemporal; Enfermedad
Newborn hearing concurrent gene screening can improve care for hearing loss: A study on 14,913 Chinese newborns
Keywords: غربالگری ژنتیکی; Newborn hearing screening; Genetic screening; mtDNA 12S rRNA; GJB2; SLC26A4;
Drosophila metalloproteases in development and differentiation: The role of ADAM proteins and their relatives
Keywords: غربالگری ژنتیکی; ADAM; Cardiogenesis; Drosophila heart morphogenesis; EMS; Genetic screening; Kuzbanian; Meltrin; Mesoderm; Neprilysin; Unc5
E-cadherin genetic screening and clinico-pathologic characteristics of early onset gastric cancer
Keywords: غربالگری ژنتیکی; Early onset gastric cancer; E-cadherin; Pathology; Diffuse gastric cancer; Hereditary and sporadic cancer; Germline mutations; Family history; Genetic screening; Second hit; Promoter methylation
Pregnancy in Cystic Fibrosis
Keywords: غربالگری ژنتیکی; Cystic fibrosis; Pregnancy; Birth outcomes; Genetic screening;
Clinical Approach to Diagnosis and Management of Ovarian, Fallopian Tube, and Peritoneal Carcinoma
Keywords: غربالگری ژنتیکی; Ovarian cancer; Fallopian tube cancer; Primary peritoneal cancer; Genetic screening; Epidemiology; Staging procedures; Cytoreductive surgery; Chemotherapy