قانون روابط خونی - «حقی» برای دسترسی به اصل و نسب ژنتیک ...
A Law of Blood-ties - The ‘Right’ to Access Genetic Anc ......
گزارشات JIMD – گزارش های موردی و تحقیقاتی، 2012/5
JIMD Reports - Case and Research Reports, 2012/5
چپرونوپاتی ها – بیماری های با چپرون های مولکولی ناقص
The Chaperonopathies - Diseases with Defective Molecula ...
ژنتیک سکته مغزی
Stroke Genetics
نسل بعدی فناوری های توالی در ژنتیک پزشکی
Next Generation Sequencing Technologies in Medical Gene ...
ژنتیک پزشکی
Medical Genetics
بررسی ژنوم انسان – بینش ها در تنوع انسان و حساسیت بیمار ...
Investigating the Human Genome...
دیزومی تک والدینی (UPD) در ژنتیک بالینی – راهنمایی برای ...
Uniparental Disomy (UPD) in Clinical Genetics...
ژن ها، الگو های رفتاری، فرهنگ، و بیماری های روانی – به ...
Genes, Memes, Culture, and Mental Illness...
راهنمای تجزیه و تحلیل داده های ژنتیک انسانی – رویکرد ها ...
Handbook on Analyzing Human Genetic Data...
سندرم آتاکسی تریمور همراه با X شکننده (FXTAS)
The Fragile X-Associated Tremor Ataxia Syndrome - FXTAS
سندرم هیوز: سندرم فسفولیپید – راهنمایی برای دانشجویان
Hughes Syndrome - The Antiphospholipid Syndrome
کروموزوم های انسانی
Human Chromosomes
تغییرات DNA در سندرم لینچ – پیشرفت ها در تشخیص مولکولی ...
DNA Alterations in Lynch Syndrome...
زیست شناسی سلولی و مولکولی اختلال ...
Cellular and Molecular Biology ...
Over the past several decades the incidence of autism spectrum disorders (ASD) has increased dramatically. the etiology of ASD remains an unsolved puz ...
آلکسی (آلکسیا، الکسی: اختلال مغزی ...
Alexia
Alexia - Diagnosis, Treatment and Theory This book is a comprehensive review of the main acquired disorders of reading: hemianopic, pure and cent ...
قانون روابط خونی - «حقی» برای دست ...
A Law of Blood-ties - The ‘Righ ...
This text collates and examines the jurisprudence that currently exists in respect of blood-tied genetic connection, arguing that the right to identit ...
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 ...
اختلالات میسفولدینگ پروتئین – سفر ...
Protein Misfolding Disorders
Protein Misfolding Disorders - A Trip into the ER Neurodegenerative disorders such as Amyotrophic lateral sclerosis (ALS), Alzheimer’s disease (A ...
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, ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
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 ...
سندرم هیوز: سندرم فسفولیپید – راه ...
Hughes Syndrome - The Antiphosp ...
Hughes Syndrome - The Antiphospholipid Syndrome - A Guide for Students Hughes Syndrome: The Antiphospholipid Syndrome, A Guide for Students provi ...
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 ...
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 ...
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 ...
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 ...
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 ...