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 ...
This Brief provides a concise review of chaperonopathies, i.e., diseases in which molecular chaperones play an etiologic-pathogenic role. Introductory ...
This extensively illustrated reference work is designed for health professionals who care for newborn infants including neonatologists, pediatricians, ...
Protein Misfolding Disorders - A Trip into the ER Neurodegenerative disorders such as Amyotrophic lateral sclerosis (ALS), Alzheimer’s disease (A ...
JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously ...
This text collates and examines the jurisprudence that currently exists in respect of blood-tied genetic connection, arguing that the right to identit ...
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 ...
