گزارشات JIMD – گزارش های موردی و پژوهشی
JIMD Reports – Case and Research Reports, 2012/3
گزارشات JIMD – گزارش های موردی و پژوهشی
JIMD Reports – Case and Research Reports, 2012/1
گزارشات JIMD – گزارش های موردی و پژوهشی
JIMD Reports – Case and Research Reports, 2011/2
بیماری دوپویترن و اختلالات هایپر پرولیفراتیو – اصول، پژ ...
Dupuytren’s Disease and Related Hyperproliferative Diso ......
ژنتیک موش
Genetics of the Mouse
ارزش تشخیصی، پیش آگهی و درمانی امضا های ژن
Diagnostic, Prognostic and Therapeutic Value of Gene Si ...
اختلالات هیستوسیتیک کودکان و بزرگسالان – علم پایه، ویژگ ...
Histiocytic Disorders of Children and Adults...
مدیریت جامع ناهنجاری های شریانی مغز و ستون فقرات
Comprehensive Management of Arteriovenous Malformations ...
ژن، درمانگاه، و خانواده – تشخیص نقص مورفولوژی (دیسمورفو ...
The Gene, the Clinic, and the Family...
تبعیض ژنتیکی
Genetic Discrimination
اپی ژنتیک و پاتولوژی – بررسی ارتباطات بین مکانیسم های ژ ...
Epigenetics and Pathology...
ناهنجاری های مادرزادی اندام فوقانی – اتیولوژی و مدیریت
Congenital Anomalies of the Upper Extremity
تغییرات DNA در سندرم لینچ – پیشرفت ها در تشخیص مولکولی ...
DNA Alterations in Lynch Syndrome...
کروموزوم های انسانی
Human Chromosomes
نقش ترانسکریپتوم در پیشگیری از سر ...
Role of the Transcriptome in Br ...
This book will provide the latest advances in molecular and cellular biology for establishing the foundation of a complete understanding of the mechan ...
گزارشات JIMD – گزارش های موردی و ...
JIMD Reports – Case and Researc ...
This book offers current case studies and short research reports in the area of inherited metabolic disorders. Coverage includes unusual or previously ...
گزارشات JIMD – گزارش های موردی و ...
JIMD Reports – Case and Researc ...
JIMD Reports publishes case and short research reports on inherited metabolic disorders. These highlight unusual or previously unrecorded features rel ...
گزارشات JIMD – گزارش های موردی و ...
JIMD Reports – Case and Researc ...
This book offers peer-reviewed case studies and short research reports in the area of inherited metabolic disorders. Coverage includes unusual or prev ...
سندرم های میلودیسپلاستیک – از پات ...
Myelodysplastic Syndromes
In spite of tremendous advances in the field, the current understanding of pathogenesis of myelodysplastic syndromes (MDS) remains limited. Furthermor ...
بیماری دوپویترن و اختلالات هایپر ...
Dupuytren’s Disease and Related ...
Dupuytren’s Disease and Related Hyperproliferative Disorders - Principles, Research, and Clinical Perspectives This book is based on results of t ...
کوچک مولکول درمانی برای بیماری ژن ...
Small Molecule Therapy for Gene ...
Thoene summarises the substantial work that has been accomplished in the treatment of inborn errors of metabolism with simple molecules. This handbook ...
ژنتیک موش
Genetics of the Mouse
This book, written by experienced geneticists, covers topics ranging from the natural history of the mouse species, its handling and reproduction in t ...
از DNA تا شناخت اجتماعی
From DNA to Social Cognition
Decision-making is an integral part of our daily lives. Researchers seek a complete understanding of the decision-making process, including the biolog ...
بیماری های متابولیک مادرزادی – تش ...
Inborn Metabolic Diseases
Being up to Date: Status Quo and Trends of Treatment --- For those involved in the identification and management of patients with inborn errors of met ...
ارزش تشخیصی، پیش آگهی و درمانی ام ...
Diagnostic, Prognostic and Ther ...
Gene expression studies have revealed diagnostic profiles and upregulation of specific pathways in many solid tumors. The explosion of new information ...
اختلالات هیستوسیتیک کودکان و بزرگ ...
Histiocytic Disorders of Childr ...
Histiocytic Disorders of Children and Adults: Basic Science, Clinical Features and Therapy As a comprehensive reference on all aspects of the his ...
مدیریت جامع ناهنجاری های شریانی م ...
Comprehensive Management of Art ...
Vascular malformations of the brain and spine pose many management challenges. This text provides a comprehensive, state-of-the-art review of the natu ...
مالفرماسیون های کاورنوس سیستم عصب ...
Cavernous Malformations of the ...
Questions regarding the nature and appropriate management of cavernous malformation (CM) have clouded researchers and those faced with making clinical ...
ژن، درمانگاه، و خانواده – تشخیص ن ...
The Gene, the Clinic, and the F ...
The Gene, the Clinic, and the Family - Diagnosing Dysmorphology, Reviving Medical Dominance While some theorists argue that medicine is caught in ...
آزمایش ژنتیک – حساب های استقلال، ...
Genetic Testing
Genetic Testing - Accounts of Autonomy, Responsibility and Blame Advances in molecular genetics have led to the increasing availability of geneti ...
تبعیض ژنتیکی
Genetic Discrimination
As genetic technologies advance, genetic testing may well offer the prospect of detecting the onset of future disabilities. Some research also forward ...
بحث ژنتیک انسانی – مسائل معاصر در ...
Debating Human Genetics
Debating Human Genetics - Contemporary Issues in Public Policy and Ethics Debating Human Genetics is based on ethnographic research focusing prim ...
اپی ژنتیک و پاتولوژی – بررسی ارتب ...
Epigenetics and Pathology
Epigenetics and Pathology: Exploring Connections Between Genetic Mechanisms and Disease Expression This important book explores recent research b ...
سندرم داون – مقدمه ای برای والدین ...
Down Syndrome
Down Syndrome - An Introduction for Parents and Carers Updated to reflect the most current information in the field, this practical reference add ...
ناهنجاری های مادرزادی اندام فوقان ...
Congenital Anomalies of the Upp ...
Congenital Anomalies of the Upper Extremity - Etiology and Management Written by leading experts in the fields of pediatrics, orthopedic surgery ...
تشخیص ژنتیکی پیش از لانه گزینی عم ...
Practical Preimplantation Genet ...
Although treatment remains the major goal in the control of genetic disease, this is not yet a reality for most inherited conditions. In the absence o ...
تغییرات DNA در سندرم لینچ – پیشرف ...
DNA Alterations in Lynch Syndro ...
DNA Alterations in Lynch Syndrome - Advances in Molecular Diagnosis and Genetic Counselling Lynch syndrome (LS) is the most common cause of inher ...
کروموزوم های انسانی
Human Chromosomes
His book presents a comprehensive introduction to the principles of human Tcytogenetics and provides examples of their applications, especially those ...
فیبروز کیستیک (سیستیک فیبروزیس) – ...
Cystic Fibrosis
Cystic Fibrosis - Diagnosis and Protocols, Volume II: Methods and Resources to Understand Cystic Fibrosis Despite the many milestones in cystic f ...