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RowTitlePresenting AuthorScientific ChapterAffiliation
1 A Novel Missence Mutation in the Transglutaminase-1 Gene in an Autosomal Recessive Congenital Ichthyosis Patient Ahmadi shadmehri Aazam تازه هاي ژنتيک و اختلالات شايع ژنتيکي Social Welfare Organization of South Khorasan Province, Birjand, Iran
2 Whole-exome sequencing (WES) provides the possibility of genome-wide preconception carrier screening Alipour Olyaei Nasrin تازه هاي ژنتيک و اختلالات شايع ژنتيکي Genomic Research Center, Shahid Beheshti University of Medical Sciences, Taleghani Hospital, Aarabi St., Yaman Ave., Velenjak, Tehran-Iran
3 Genetic causes of premature ovarian failure Almadani Seyed navid تازه هاي ژنتيک و اختلالات شايع ژنتيکي Department of Genetics,Reproductive Biomedicine Reserch Center ,Royan Institute for Reproductive Biomedicine , ACECR ,Tehran, Iran
4 Effects of familial hypercholesterolemia-associated genes on the phenotype of premature myocardial infarction. Asadi Seyed ehsan تازه هاي ژنتيک و اختلالات شايع ژنتيکي phd of Nursing, Esfahan Medical University, Esfahan, Iran.
5 ازدواج فامیلی و اختلالات ژنتیکی Asadpour Shaghayegh تازه هاي ژنتيک و اختلالات شايع ژنتيکي دانشگاه آزاد اسلامی بابل
6 The robust bioinformatics pipeline and comprehensive clinical review of patients with genetic disorders significantly improve overall diagnosis by exome sequencing Bahreini Amir تازه هاي ژنتيک و اختلالات شايع ژنتيکي Karyogen, Isfahan, IRAN
7 Role of the clinical genetic databases in a better performance of genetic counseling Falah Masoumeh تازه هاي ژنتيک و اختلالات شايع ژنتيکي ENT and Head & Neck Research Center and Department, The Five Senses Institute, Hazrat Rasool Akram Hospital, Iran University of Medical Sciences, Tehran, Islamic Republic of Iran;
8 DOCK8-related immunodeficiency syndrome (DIDS): novel deleterious mutations Gharesouran Jalal تازه هاي ژنتيک و اختلالات شايع ژنتيکي Division of Medical Genetics, Tabriz Children's Hospital, Tabriz University of Medical Sciences, Tabriz, Iran.
9 SPINK5 and Netherton syndrome: novel deleterious mutation Gharesouran Jalal تازه هاي ژنتيک و اختلالات شايع ژنتيکي Molecular Genetics Division, GMG center, Tabriz, Iran
10 Comparison and comparison of telomerase expression in healthy tissue and breast cancer Igder Mohsen تازه هاي ژنتيک و اختلالات شايع ژنتيکي Tabriz university
11 Diagnosis of lethal or prenatal-onset or familial coinciding recessive disorders by parental exome sequencing Jamali Payman تازه هاي ژنتيک و اختلالات شايع ژنتيکي Aliakbar genetic counseling center, Shahrood welfare office, Shahrood, Iran
12 Carrier detection of CAH, in a consanguineous family with a deseased affected child Jazayeri Roshanak تازه هاي ژنتيک و اختلالات شايع ژنتيکي Department of Genetics, Faculty of Medicine, Alborz University of Medical Sciences, Karaj, Iran
13 New Phenotypes for Old Genes Kariminejad Ariana تازه هاي ژنتيک و اختلالات شايع ژنتيکي Chief Genetic Counselor
14 The first world report of a homozygous mutation in Pseudouridine synthase-3 gene (PUS3) in two patients with intellectual disability in an Iranian family Keshavarz Parvaneh تازه هاي ژنتيک و اختلالات شايع ژنتيکي Genetics Medical Laboratory of Dr Keshavarz, Rasht, Iran- School of Medicine (Department of Genetics), Guilan University of Medical Science, Rasht, Iran
15 Association of a genetic variant in Interleukin-10 gene with increased risk and inflammation associated with cervical cancer Maftouh Mina تازه هاي ژنتيک و اختلالات شايع ژنتيکي Mashhad University of Medical Sciences
16 شناسایی موتاسیون جدید (c.1006C>T) در ژن SPG20 مرتبط با سندروم Troyer Mahdavi Mohammad Reza تازه هاي ژنتيک و اختلالات شايع ژنتيکي دانشگاه علوم پزشکی مازندران
17 شناسایی موتاسیون جدید در ژن AIPL1 همبسته با بیماری Leber Congeital Amaurosis Mahdavi Mohammad Reza تازه هاي ژنتيک و اختلالات شايع ژنتيکي دانشگاه علوم پزشکی مازندران
18 LAMA1 gene variant associated with intellectual disability and sever myopia - a case report Moghbelinejad Sahar تازه هاي ژنتيک و اختلالات شايع ژنتيکي 3Cellualr and molecular research center, Qazvin university of medical science, Qazvin, IRAN.
19 Genetic Approach to Recurrent Pregnancy Loss Pooladi Arash تازه هاي ژنتيک و اختلالات شايع ژنتيکي 1- Cellular and Molecular Research Center, Medical Genetics and Molecular Medicine Department, Kurdistan University of Medical Sciences, Sanandaj, Iran.
20 Characterization of human papillomavirus (HPV) genotypes among patients referred to gynecology clinic, Laleh hospital, Tehran, Iran. Rezaei IMAN تازه هاي ژنتيک و اختلالات شايع ژنتيکي مركز ژنتيك بيمارستان لاله و پژوهشگاه بيماريهاي ويروسي، بخش تشخيص مولكولي
21 بررسی و مقایسه بیان آنزیم تلومراز در بافت سالم و بافت سرطانی پستان¬ها Rezvani Zahra sadat تازه هاي ژنتيک و اختلالات شايع ژنتيکي دانشجوی کارشناسی ارشد رشته زیست شناسی، گرایش ژنتیک، دانشگاه آزاد اسلامی واحد علوم و تحقیقات آذربایجان شرقی
22 اختلالات متابولیسم ارثی Shahzadeh fazeli Seyed abolhassan تازه هاي ژنتيک و اختلالات شايع ژنتيکي Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
23 Two variants in exon and intron 9 of LDLR gene in Iranian familial hypercholesterolemia patients Tajamolian Masoud تازه هاي ژنتيک و اختلالات شايع ژنتيکي Medical Genetic Research Center, Shahid Sadoughi University of Medical science, Yazd,Iran
24 آنالیز پیوستگی لوکوس در ناشنوایان DFNB77 و DFNB37 های غیر سندرومی با وراثت اتوزومال مغلوب در استان هرمزگان Ahmadi Banafsheh تازه هاي ژنتيک و اختلالات شايع ژنتيکي Medical Biotechnology Resarch Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd
25 : شناسایی جهش A1298C ژن MTHFR در مردان نابارور Darvishi Maryam تازه هاي ژنتيک و اختلالات شايع ژنتيکي دانشگاه آزاد اسلامی واحد دزفول
26 سندرم داون و آزمایشات قبل از تولد برای شناسایی آن Fakeri Mahsa تازه هاي ژنتيک و اختلالات شايع ژنتيکي دانشگاه سراسری تبریز
27 Determine a mutation in a daughter suffer from hydrocephalus and developmental disorder Ghavabesh Jassem تازه هاي ژنتيک و اختلالات شايع ژنتيکي Center of Geneics consulation of Ahwaz Behzisti
28 Investigation and Comparison of margin and tumor in breast cancer patient (lominal A) by proteomic approach Khani Ramtin تازه هاي ژنتيک و اختلالات شايع ژنتيکي Young Researchers and Elite club, Azad Islamic University, Medical science branch, Tehran, Iran
29 Detection of a new pathogenic mutation on DMD gene associated with Duchene Muscular Dystrophy Mohaddes Ardebili Seied Vahid تازه هاي ژنتيک و اختلالات شايع ژنتيکي Cytogenetics Division, Dr. Mohaddes Medical Genetics Laboratory (DMMGL), Tabriz, Iran
30 Association of A Novel Balanced Reciprocal Translocation and Recurrent Miscarriage: A Case Report Mohaddes Ardebili Seied Vahid تازه هاي ژنتيک و اختلالات شايع ژنتيکي Cytogenetics Division, Dr. Mohaddes Medical Genetics Laboratory (DMMGL), Tabriz, Iran
31 A brief view on the role of genetic counseling in neuromuscular disease Sadeghinia Farnaz تازه هاي ژنتيک و اختلالات شايع ژنتيکي Genetics research center, University of social welfare and rehabilitation sciences, Tehran, Iran
32 Case Report of Bardet Biedl Syndrome Sorkhkooh Azari Noushin تازه هاي ژنتيک و اختلالات شايع ژنتيکي Allame Amini Genetic Consultant Center, Tabriz, Iran
33 Effects of N-acetyl-cysteine supplementation on sperm quality, chromatin integrity and level of oxidative stress in infertile men. Asadi Seyed ehsan ديس مورفولوژي phd of Nursing, Esfahan Medical University, Esfahan, Iran.
34 Deletion 22q11.2 syndrome frequency in patients with cleft palate referred to Alzahra Hospital, Isfahan, Iran Nejati Omid ديس مورفولوژي 22 Bahman Hospital- Medical and Pathological laboratory - Islamic Azad University of Mashhad, Iran
35 A Case report of Expanding the clinical spectrum of Van Maldergem Syndrome in Hasti genetic counselling centre in south Khorasan Rezazadeh Jamileh ديس مورفولوژي اداره کل بهزیستی خراسان جنوبی
36 اثربخشی آموزش مهارت‌های ارتباطی بر بهبود کیفیت زندگی افراد کم بینای آرپی Mozafari HOSEIN نابينايي آموزش وپرورش استثنایی
37 Application of multi-gene panel in juvenile-onset glaucoma: report of 2 cases with dominant & recessive inheritance Vahedi Afsaneh نابينايي Mana genetic counseling center, Shahrood, Iran.
38 Maternal circulating microRNAs as non-invasive biomarkers for prenatal diagnosis of congenital heart defects Abtin Maryam اختلالات قلبي – عروقي Department of medical genetics, Faculty of medicine, Tabriz university of medical sciences,Tabriz, Iran
39 بررسی علل مرگ کودکان 59-1 ماهه ناشی از ناهنجاری مادرزادی در بخش خارج بیمارستانی دانشگاه علوم پزشکی تبریز ولزوم انجام مشاوره ژنتیک Ansari Masoumeh اختلالات قلبي – عروقي معاونت بهداشت دانشگاه علوم پزشکی تبریز
40 Randomized, double-blind, placebo-controlled clinical trial of choline supplementation in school-aged children with fetal alcohol spectrum disorders. Asadi Seyed ehsan تراتولوژي phd of Nursing, Esfahan Medical University, Esfahan, Iran.
41 تحلیل روابط "تنظیم هیجانی"،"بهزیستی روانشناختی" ،"ریسک فاکتورهای قلبی در بیماران مبتلا به سکته قلبی Ghobadi Soroush اختلالات قلبي – عروقي سازمان بهزیستی
42 Association of a genetic variant in the angiopoietin-like protein 4 gene with metabolic syndrome. Avan Amir اختلالات قلبي – عروقي Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
43 Rare P376L variant in the SR-BI gene associates with HDL dysfunction and risk of cardiovascular disease Avan Amir اختلالات قلبي – عروقي Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
44 Bioinformatics study and genetic counseling contribute to the diagnosis of cardiovascular disorders Mansouri Fatemeh اختلالات قلبي – عروقي Department of Genetics and Immunology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
45 The study of KCNE1 gene mutations in Iranian LQTS patients Norouzi Rambod اختلالات قلبي – عروقي 1-Rajaie Cardiovascular Medical and Research Center, Iran University of Medical Sciences, Tehran, Iran 2- Department of Biology, Faculty of Basic Science, Kharazmi University, Tehran, Iran
46 A novel large exon deletion in GFAP gene, Adult Alexander disease in Iran; The first report in the world Alizadeh Fatemeh Other related topics Genomic Psychiatry Department, Roozbeh Hospital, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
47 بررسی وضعیت موجود تشخیص ناهنجاریهای مادرزادی با انجام سونوگرافی دردانشگاه علوم پزشکی تبریز Ansari Masoumeh Other related topics معاونت بهداشت دانشگاه علوم پزشکی تبریز
48 Effect of inorganic polyphosphate on microvascular endothelial permeability and its mechanism: focus on AMP kinase signaling pathway Avan Amir Other related topics Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
49 Genetic Consultation, Genomics Techniques and further in-vitro fertilization Strategies in families with a child involved with auto-immune hemolytic disorders Banihashemi Kambiz Other related topics Academic member, ATU, MSRT, Tehran, Iran
50 preferencing 4p medicnes Darsaneh Zahra Other related topics azad babol university
51 جنبه های بالینی تفسیر کلینیکال داده های WES در جمعیت ایرانی Dastmalchi Romina Other related topics دانشگاه علوم پزشکی شهید بهشتی
52 Associated genes with early and late onset of symptoms in patients with Charcot–Marie–Tooth disease Gharesouran Jalal Other related topics Division of Medical Genetics, Tabriz Children's Hospital, Tabriz University of Medical Sciences, Tabriz, Iran
53 مشاوره ویژه ژنتیک ناباروری در مردان آزواسپرمیک با اختلالات کروموزومی و حذف های جزئی در ناحیه AZF Montazeri Somayeh Other related topics دانشجوی دکترای ژنتیک، مرکز تحقیقات ژنتیک تالاسمی،هموفیلی و تشخیص قبل از تولد، بیمارستان آیت الله شهید دستغیب دانشگاه علوم پزشکی شیراز،شیراز، ایران
54 The role of genetic counseling in the prevention of hearing loss in Iranian patients Morovvati Saeid Other related topics Human Genetic Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran.
55 Association of heteromorphism of chromosome 9 and recurrent abortion (ultrasound diagnosed blighted ovum) Nazarabadi Mohamad Other related topics MASSHAD University of Medical Science Department Of medical Genetic & polyclinic Genetics Of Nasle Omid
56 نتایج 381 مورد آمنیوسنتز Reyhanifar Farahnaz Other related topics بیمارستان فوق تخصصی بهبود
57 بایدهاونبایدهای تست های غربالگری ئوران بارداری Reyhanifar Farahnaz Other related topics سازمان بهزیستی
58 spinocerbellar ataxia Sahebalzamani Afsaneh Other related topics kerman Welfare organization
59 Glioblastomas and Genetic Counseling Salmani Tayyebali Other related topics Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran
60 The gene association between obesity and type 2 diabetes Sheikhpour Mojgan Other related topics Department of Mycobacteriology and Pulmonary Research, Pasteur Institute of Iran, Tehran, Iran.
61 Association between four novel miRNAs polymorphisms and susceptibility to idiopathic recurrent spontaneous abortion Hosseinzadeh Asghar Other related topics Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran
62 Cytogenetic investigation and Clinical Phenotype of patients with primary amenorrhea in Kermanshah Province, west of Iran Jalilian Nazanin Other related topics department of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical Sciences
63 Expression of CAPN11 and UBQLN3 in non-obstructive azoospermia Karimi Masoumeh Other related topics department of mesenchymal stem cell, academic center for education culture and researc, Qom, Iran.
64 AMP-kinase inhibitor dorsomorphin reduces the proliferation and migration behavior of colorectal cancer cells by targeting the AKT/mTOR Pathway Maftouh Mina Other related topics Metabolic syndrome Research center, Mashhad University of Medical Sciences, Mashhad, Iran
65 Comparison of neonatal blood glucose of diabetic mothers who took hypoglycemic drug and diabetic mothers who did not take medication at Buali Hospital 2017 – 2018 Mohammadnuri Marjan Other related topics Pediatrician , Assistant professor , Pediatric Department ,Tehran Medical sciences Branch , Islamic Azad University , Tehran , Iran
66 Repot on a Second Case of Cockayne Syndrome in Zanjan Province due to a Missense Mutation in ERCC6 Gene Nikfar Ali Other related topics Zanjan Metabolic Diseases Research Center, Zanjan University of Medical Sciences, Zanjan, Iran
67 The Impotance of The Genetic Counseling Rahimi Maryam Other related topics The Genetic Research Center, The University of Social Welfare and Rehabilitation Sciences, Tehran, Iran
68 Phelan-McDermid syndrome presenting with developmental delays: a case reaport Yousefipour Faride Other related topics مرکز مشاوره ژنتیک دولتی بهزیستی


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