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
مشاوره ژنتیک برای بیماری نوروژنتیک بزرگسالان – کتاب مور ...
Genetic Counseling for Adult Neurogenetic Disease...
تغییرات DNA در سندرم لینچ – پیشرفت ها در تشخیص مولکولی ...
DNA Alterations in Lynch Syndrome...
کروموزوم های انسانی
Human Chromosomes
سندرم آتاکسی تریمور همراه با X شکننده (FXTAS)
The Fragile X-Associated Tremor Ataxia Syndrome - FXTAS
راهنمای تجزیه و تحلیل داده های ژنتیک انسانی – رویکرد ها ...
Handbook on Analyzing Human Genetic Data...
ژن ها، الگو های رفتاری، فرهنگ، و بیماری های روانی – به ...
Genes, Memes, Culture, and Mental Illness...
دیزومی تک والدینی (UPD) در ژنتیک بالینی – راهنمایی برای ...
Uniparental Disomy (UPD) in Clinical Genetics...
بررسی ژنوم انسان – بینش ها در تنوع انسان و حساسیت بیمار ...
Investigating the Human Genome...
ژنتیک پزشکی
Medical Genetics
نسل بعدی فناوری های توالی در ژنتیک پزشکی
Next Generation Sequencing Technologies in Medical Gene ...
ژنتیک سکته مغزی
Stroke Genetics
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 ...
مشاوره ژنتیک برای بیماری نوروژنتی ...
Genetic Counseling for Adult Ne ...
Genetic Counseling for Adult Neurogenetic Disease - A Casebook for Clinicians The adult patient diagnosed with or at risk for a neurogenetic dise ...
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 ...
سندرم آتاکسی تریمور همراه با X شک ...
The Fragile X-Associated Tremor ...
In Fragile X-Associated Tremor Ataxia Syndrome (FXTAS), the editors present information on all aspects of FXTAS, including clinical features and curre ...
راهنمای تجزیه و تحلیل داده های ژن ...
Handbook on Analyzing Human Gen ...
Handbook on Analyzing Human Genetic Data - Computational Approaches and Software This handbook offers guidance on selections of appropriate compu ...
ژن ها، الگو های رفتاری، فرهنگ، و ...
Genes, Memes, Culture, and Ment ...
Genes, Memes, Culture, and Mental Illness - Toward an Integrative Model What produces mental illness: genes, environment, both,neither? The answe ...
دیزومی تک والدینی (UPD) در ژنتیک ...
Uniparental Disomy (UPD) in Cli ...
Uniparental Disomy (UPD) in Clinical Genetics - A Guide for Clinicians and Patients This book focus on genetic diagnostics for Uniparental Disomy ...
بررسی ژنوم انسان – بینش ها در تنو ...
Investigating the Human Genome
Investigating the Human Genome - Insights into Human Variation and Disease Susceptibility An Up-to-Date Assessment of Recent Advances in Human Ge ...
ژنتیک پزشکی
Medical Genetics
A complete introductory text on how to integrate basic genetic principles into the practice of clinical medicine. Medical Genetics is the first text t ...
عقلانیت و چالش ژنتیک – ایجاد مردم ...
Rationality and the Genetic Cha ...
Rationality and the Genetic Challenge - Making People Better Should we make people healthier, smarter, and longer-lived if genetic and medical ad ...
تنوع ژنتیکی انسانی – پیامد های عم ...
Human Genetic Diversity
Human Genetic Diversity - Functional Consequences for Health and Disease This book describes the remarkable progress which has been made in defin ...
نسل بعدی فناوری های توالی در ژنتی ...
Next Generation Sequencing Tech ...
This book introduces readers to Next Generation Sequencing applications in medical genetics. The authors discuss the direct application of next-genera ...
آیا من ژن های من هستم؟ – مقابله ب ...
Am I My Genes?
Am I My Genes? - Confronting Fate and Family Secrets in the Age of Genetic Testing In the fifty years since DNA was discovered, we have seen extrao ...
درسنامه ژنتیک تولید مثل انسانی
Textbook of Human Reproductive ...
What happens with our genome and epigenome in the first fundamental days of our development? How can this be analysed? What do we need to know when fa ...
ژنتیک سکته مغزی
Stroke Genetics
Over the last decade there has been a substantial increase in our understanding of the genetic basis of common disorders such as stroke. Stroke Geneti ...
چپرونوپاتی ها – بیماری های با چپر ...
The Chaperonopathies - Diseases ...
This Brief provides a concise review of chaperonopathies, i.e., diseases in which molecular chaperones play an etiologic-pathogenic role. Introductory ...
ناهنجاری های رایج (مالفرماسیون ها ...
Common Malformations
This extensively illustrated reference work is designed for health professionals who care for newborn infants including neonatologists, pediatricians, ...
گزارشات JIMD – گزارش های موردی و ...
JIMD Reports - Case and Researc ...
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously ...