Keywords: مشاوره ژنتیکی; Prenatal diagnosis; Trisomy 8; Mosaicism; Outcome; Genetic counselling;
مقالات ISI مشاوره ژنتیکی (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: مشاوره ژنتیکی; Reproductive genetic screening; Prenatal testing; Genetic counselling; Cell-free DNA; Non-invasive prenatal testing; Informed decision-making;
Keywords: مشاوره ژنتیکی; Genetic counselling; Counselling model; Autism Spectrum Disorder; Genetics of Autism Spectrum Disorder;
Keywords: مشاوره ژنتیکی; Complex chromosome rearrangement; Genetic counselling; Next-generation sequencing; Preimplantation genetic testing;
Keywords: مشاوره ژنتیکی; Genetic counselling; Mosaicism; Next-generation sequencing; Preimplantation genetic screening; Prenatal diagnosis;
Keywords: مشاوره ژنتیکی; Donación de ovocitos; Cribado genético; Enfermedades autosómicas recesivas; Asesoramiento genético; Oocyte donation; Extended carrier screening; Autosomal recessive diseases; Genetic counselling;
Keywords: مشاوره ژنتیکی; preconception care; prenatal care; genetic counselling; genetic testing; mass screening; folic acid;
Keywords: مشاوره ژنتیکی; Karyotype; Balanced translocation; Gene disrupted; Developmental abnormalities; Genetic counselling
Keywords: مشاوره ژنتیکی; Array comparative genomic hybridization; congenital heart defects; prenatal diagnosis; genetic counselling; CGH; comparative genomic hybridization; CHD; congenital heart disease; CNV; copy number variant; FISH; fluorescence in situ hybridization; VOUS; va
Keywords: مشاوره ژنتیکی; adrenocortical carcinoma; genetic counselling; hereditary cancer syndromes; medical genetics; paraganglioma; pheochromocytoma
Keywords: مشاوره ژنتیکی; Congenital heart disease; Genetic counselling; Genetics education; Intervention; Guilt and shame; Psychological stress
Keywords: مشاوره ژنتیکی; Epilepsy; Genetics; Qualitative research; Genetic testing; Genetic counselling
Keywords: مشاوره ژنتیکی; Carrier testing; Minors; Carrier screening; Genetic counselling
Keywords: مشاوره ژنتیکی; Congenital pulmonary lymphangiectasis; Review; Classification; Diagnosis; Therapeutic options; Genetic counselling
Keywords: مشاوره ژنتیکی; Breast cancer; Genetic counselling; Communication; Interaction analysis;
Keywords: مشاوره ژنتیکی; Lynch syndrome; Genetic counselling; Developing country; Communication; Qualitative; Predictive testing;
Keywords: مشاوره ژنتیکی; Glioma; Familial glioma; Clinical characteristics; Genetic counselling;
Surprisingly good outcome in antenatal diagnosis of severe hydrocephalus related to CCDC88C deficiency
Keywords: مشاوره ژنتیکی; Congenital hydrocephalus; CCDC88C; Brain malformation; Autosomal recessive; Reproductive medicine; Genetic counselling; Molecular genetics;
Utilidad del estudio molecular de la hipercalcemia hipocalciúrica familiar; detección de una nueva mutación genética
Keywords: مشاوره ژنتیکی; Hipercalcemia hipocalciúrica familiar; Gen CASR; Hiperparatiroidismo primario; Hiperparatiroidismo neonatal grave; Asesoramiento genético; Familial hypocalciuric hypercalcemia; CASR gene; Primary hyperparathyroidism; Severe neonatal hyperparathyroidism;
Discusión ética y legal del asesoramiento genético en paciente portadora de una variación patológica en RAD51D
Keywords: مشاوره ژنتیکی; RAD51D; Cáncer hereditario de mama; Cáncer hereditario de ovario; BRCA1; BRCA2; Asesoramiento genético; Aspectos ético-legales; RAD51D; Hereditary breast cancer; Hereditary ovarian cancer; BRCA1; BRCA2; Genetic counselling; Ethical-legal aspects;
Original ResearchOnline self-test identifies women at high familial breast cancer risk in population-based breast cancer screening without inducing anxiety or distress
Keywords: مشاوره ژنتیکی; Breast cancer; Population screening; BRCA1; BRCA2; Hereditary; Risk; Familial risk assessment; Genetic counselling; Distress; Prevention;
Consejo genético oncológico: las aplicaciones de la Psicooncología
Keywords: مشاوره ژنتیکی; Psicooncología; Consejo genético; CáncerPsycho-oncology; Genetic counselling; Cancer
Comparing the ability of OPTION12 and OPTION5 to assess shared decision-making in genetic counselling.
Keywords: مشاوره ژنتیکی; Shared decision-making; OPTION instrument; Genetic counselling; Decisional conflict; Anxiety; Informed decision-making
Antenatal counselling for congenital anomaly tests: Pregnant Muslim Moroccan women׳s preferences
Keywords: مشاوره ژنتیکی; CT; combined test; FAS; fetal anomaly scan; Genetic counselling; Antenatal diagnosis; Islam; Needs assessment; Down syndrome; Personal autonomy;
Le syndrome de Van der Woude : une entité clinique méconnue
Keywords: مشاوره ژنتیکی; Syndrome de Van der Woude; IRF6; Conseil génétiqueVan der Woude syndrome; IRF6; Genetic counselling
SÃndromes de Prader-Willi y de Angelman. Expriencia de 21 años
Keywords: مشاوره ژنتیکی; Impronta genómica; Deleción; DisomÃa uniparental; Consejo genético; Metilación; Genomic imprinting; Deletion; Uniparental dysomy; Genetic counselling; Methylation;
Identification of Familial Adenomatous Polyposis carriers among children with desmoid tumours
Keywords: مشاوره ژنتیکی; Desmoid tumour; Aggressive fibromatosis; APC; β-Catenin; CTNNB1; FAP; Genetic counselling;
Chromosomal aberrations in 2000 couples of Indian ethnicity with reproductive failure
Keywords: مشاوره ژنتیکی; chromosomal aberrations; genetic counselling; infertility; karyotyping; recurrent spontaneous abortions; reproductive failure
Guidelines for molecular diagnosis of Charcot-Marie-Tooth disease
Keywords: مشاوره ژنتیکی; Axon; Charcot-Marie-Tooth disease; Clinical guideline; Dejerine–Sottas disease; Genetic counselling; Gene mutation; Genetic neuropathy; Molecular diagnosis; Myelin; Motor nerve conduction velocityAxón; Consejo genético; Diagnóstico molecular; Enfermedad d
Delayed diagnosis and underreporting of congenital anomalies associated with oral clefts in the Netherlands: A national validation study
Keywords: مشاوره ژنتیکی; Cleft lip; Cleft palate; Congenital abnormalities; Registry; Genetic counselling
Hereditary Hearing Loss: Genetic Counselling
Keywords: مشاوره ژنتیکی; Genetic counselling; Hereditary hearing loss; Deafness; Sensorineural hearing loss; Syndromic hearing loss; Nonsyndromic hearing loss; GJB2Consejo genético; Hipoacusia hereditaria; Sordera; Hipoacusia neurosensorial; Hipoacusia sindrómica; Hipoacusia no s
Non-syndromic malformations of the central nervous system in twin pregnancies: diagnostic and other clinical features of importance
Keywords: مشاوره ژنتیکی; Twin pregnancy; Genetic counselling; Malformation of the central nervous system; Selective termination of pregnancy; Induced abortion
Prenatal cytogenetic diagnosis in Spain: analysis and evaluation of the results obtained from amniotic fluid samples during the last decade
Keywords: مشاوره ژنتیکی; Karyotype; Prenatal diagnosis; Ultrasound abnormalities; Nuchal translucency; Genetic counselling;
Azoospermia and paternal autosomal ring chromosomes: case report and literature review
Keywords: مشاوره ژنتیکی; azoospermia; cryptozoospermia; genetic counselling; male infertility; oligozoospermia; ring chromosomes
NOTCH3 gene mutations in subjects clinically suspected of CADASIL
Keywords: مشاوره ژنتیکی; NOTCH3; CADASIL; Stroke; Genetic variations; Genetic counselling;
Avances en el diagnóstico molecular de la enfermedad de Wilson
Keywords: مشاوره ژنتیکی; Enfermedad de Wilson; Degeneración hepatolenticular; Mutación; Asesoramiento genético; Secuenciación; Diagnóstico molecular; Diagnóstico prenatal; Wilson's disease; Hepatolenticular degeneration; Mutation; Genetic counselling; Sequencing; Molecular
Thrombocytopenia-absent radius (TAR) syndrome: A clinical genetic series of 14 further cases. Impact of the associated 1q21.1 deletion on the genetic counselling
Keywords: مشاوره ژنتیکی; TAR syndrome; Radial aplasia; 1q21.1 deletion; Genetic counselling; Prenatal diagnosis
PICOGEN: Five years experience with a genetic counselling program for dementia
Keywords: مشاوره 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
PICOGEN: experiencia de 5 años de un programa de asesoramiento genético en demencia
Keywords: مشاوره 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
Genetic counselling in Neurology: A complex problem that requires regulation
Keywords: مشاوره ژنتیکی; Genetic tests; Genetic counselling; Neurogenetics; Legislation; Rare disorders; Predictive testing; Análisis genéticos; Asesoramiento genético; Neurogenética; Legislación; Enfermedades raras; Test predictivos;
Neonatal abdominal wall defects
Keywords: مشاوره ژنتیکی; Fetal diagnosis; Gastroschisis; Genetic counselling; Omphalocele
Stratégies de dépistage de l'adénocarcinome pancréatique chez les patients à haut risque
Keywords: مشاوره ژنتیکی; cancer du pancréas; cancer pancréatique familial; conseil génétique; échoendoscopie; pancreatic cancer; familial pancreatic cancer; genetic counselling; endoscopic ultrasound;
Childhood phaeochromocytoma and paraganglioma: 100% incidence of genetic mutations and 100% survival
Keywords: مشاوره ژنتیکی; Phaeochromocytoma; Paraganglioma; Genetic counselling
Non-mosaic trisomy 20 of paternal origin in chorionic villus and amniotic fluid also detected in fetal blood and other tissues
Keywords: مشاوره ژنتیکی; Prenatal diagnosis; Trisomy 20; Mosaicism; Genetic counselling
Genetic Counselling Issues in Cystic Fibrosis
Keywords: مشاوره ژنتیکی; cystic fibrosis; genetic counselling; newborn screening; prenatal diagnosis; classification of CFTR mutations
Capacidad predictiva del modelo BCRAPro frente al profesional de enfermerÃa en la selección de candidatos a estudio genético de cáncer de mama u ovario hereditario
Keywords: مشاوره ژنتیکی; EnfermerÃa; Consejo genético; Modelos predictivos; Cáncer de mama; Cáncer de ovario; Nurse; Genetic counselling; Predictive models; Breast cancer; Ovarian cancer;
Sperm FISH analysis in two healthy infertile brothers with t(15;18) unbalanced translocation: Implications for genetic counselling and reproductive management
Keywords: مشاوره ژنتیکی; ART; Genetic counselling; Infertility; Sperm FISH; Unbalanced translocation
Fragile X syndrome prenatal diagnosis: parental attitudes and reproductive responses
Keywords: مشاوره ژنتیکی; Fragile X syndrome; genetic counselling; molecular diagnosis; prenatal;
Postępy w leczeniu zespołu łamliwego chromosomu X
Keywords: مشاوره ژنتیکی; zespół łamliwego chromosomu X; terapia behawioralna; leczenie wspomagające; poradnictwo genetycznefragile X syndrome; behavioural therapy; supporting treatment; genetic counselling
Hereditary Renal Cancer Syndromes: An Update of a Systematic Review
Keywords: مشاوره ژنتیکی; Birt-Hogg-Dubé syndrome; Constitutional chromosome 3 translocations; Genetic counselling; Hereditary cancer; Hereditary leiomyomatosis renal cell carcinoma; Hereditary papillary renal cell carcinoma; Kidney cancer; Renal cell carcinoma; Tuberous sclerosis