Alexia - Diagnosis, Treatment and Theory This book is a comprehensive review of the main acquired disorders of reading: hemianopic, pure and cent ...
Over the past several decades the incidence of autism spectrum disorders (ASD) has increased dramatically. the etiology of ASD remains an unsolved puz ...
اختلال هماهنگی رشدی (developmental coordination disorder) یا DCD که به عنوان دیسپراکسی یا دیسپراکسیای رشد و نموی (dyspraxia) نیز نامیده می شود، با عنو ...
Congenital hip disease (CHD) is the main cause of secondary osteoarthritis (OA) of the hip in young adults, which accounts for almost 40% of all cases ...
Timing, racing, combating, struggling and targeting are some actions through which cellular fate could be reflected and evaluated. Interaction between ...
In this thoroughly revised and expanded third edition of the highly praised classic, The Principles of Clinical Cytogenetics, a panel of hands-on expe ...
A comprehensive review of the recent developments in DNA repair research that have potential for translational applications. The book explains in deta ...
Human Genetics: From Molecules to Medicine provides balanced coverage of molecular and clinical genetics for the preclinical medical student with rele ...
Androgens and androgen receptors (AR) play critical roles in the development and progression of prostate cancer, the most frequently diagnosed cancer ...
Important scientific discoveries and ever-changing guidelines for how to identify and manage patients with hereditary cancer syndromes are constantly ...
Preimplantation genetic diagnosis (PGD) is a rapidly advancing field of reproductive genetics. With the significant improvements achieved over the las ...
This 6th Edition of Genetic Disorders and the Fetus maintains it's pre-eminence as the major repository of facts about prenatal diagnosis. It provides ...
Events of reproduction occurring from meiotic resumption of the immature oocyte up to its exit from the second meiotic block following activation will ...
Between the Lines of Genetic Code lays out methodologies and tools for the measurement and evaluation of gene-gene and gene-environment studies and gi ...
تغییرپذیری های کپی نامبر میکروسکوپی و ساب میکروسکوپی (CNV ها) در ژنتیک و مشاوره
The present book is an in-depth synopsis of recent advances in the fragile X field. The fragile X syndrome (FXS) is the most common form of inherited ...
EB یا اپیدرمولیز بولوزا (Epidermolysis Bullosa) یک بیماری وراثتی بافت همبند است، که باعث تاول در پوست و مخاط می گردد. این بیماری ناشی از یک نقص در نگه ...
Written by one of the most consulted authorities on the subject, Atlas of Developmental Field Anomalies of the Human Skeleton is the pre-eminent resou ...
The Philadelphia Chromosome: A Mutant Gene and the Quest to Cure Cancer at the Genetic
اختلالات ژنتیکی در کودکان می تواند اثرات بسیار متغیری داشته باشد. حتی اختلالات نسبتا شایع ممکن است توسط پزشکانی که با طیف وسیعی از علائم شناختی یا رفت ...
الگوهای قابل تشخیص دفرماسیون انسانی اسمیت، تنها کتاب اختصاص داده شده به تشخیص و مدیریت نقائص هنگام تولد ناشی از نیروهای مکانیکی در اواخر دوره بارداری ...
