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Renal genetic disorders may become apparent at any time in life and recognition of specific renal disorders is important in allowing accurate genetic ...Lees meer
This is the third edition of the foremost medical reference on hereditary hearing loss. Chapters on epidemiology, embryology, non-syndromic hearing lo...Lees meer
Duchenne Muscular Dystrophy, an inherited and progressive muscle wasting disease, is one of the most common single gene disorders found in the develop...Lees meer
This reference work should prove relevant, not only to to the student seeking a basic understanding of a particular disease, but also to the physician...Lees meer
Designed for GPs, obstetricians and paediatricians, this reference work on foetal medicine is firmly rooted in clinical practice and based on many yea...Lees meer
There have been many exciting advances in our understanding of mammalian sex determination and differentiation in the last decade. Using these advance...Lees meer
The first edition of Genomics and Clinical Medicine provided an overview of genomics-based advances in disease susceptibility, diagnosis, and predicti...Lees meer
The third edition of Human Malformations and Related Anomalies is a comprehensive reference and clinical guide to significant human malformations. Aut...Lees meer
Psychosocial issues are integral to all genetic counseling interactions. They include counselees' beliefs about the cause of birth defects and genetic...Lees meer
This fully revised and updated edition of GENETIC SKIN DISORDERS reflects the most current understanding of the diagnosis, treatment, genetic basis, a...Lees meer
When rediscovered at the turn of the century, Mendel's laws were found to be applicable to humans, but from the beginning they were fraught with probl...Lees meer
The fourth edition of the preeminent resource on Huntington's disease is a comprehensive resource on the current knowledge base surrounding this disea...Lees meer
Features information on the subject of mental retardation and developmental delay, and applies it to clinical medicine, providing information useful t...Lees meer
With the accelerating discovery of human genes, public health professionals are increasingly confronted with a large body of scientific information th...Lees meer
Obesity is one of the most important contributing factors to disease throughout the world and is an area of great current interest among researchers a...Lees meer
Advances in genetics over the past 50 years have been dramatically changed the understanding and management of inherited disorders, and are beginning ...Lees meer
Several general principles have emerged from the study of human transcription factors. First, germline mutations in genes encoding transcription facto...Lees meer
This book is a new addition to the Oxford Monographs on Medical Genetics series, providing a comprehensive review of the area of mitochondrial genetic...Lees meer
Many diseases of the nervous system are difficult to treat but can be prevented when we have adequate genetic information. This work covers the geneti...Lees meer
Overgrowth Syndromes is a comprehensive clinical guide to the well-defined genetic disorders (and others that are less well-defined) for which somatic...Lees meer