Ben je op zoek naar creating conditions the making and remaking of a genetic syndrome? Bekijk onze boeken selectie en zie direct bij welke webshop je creating conditions the making and remaking of a genetic syndrome online kan kopen. Ga je voor een ebook of paperback van creating conditions the making and remaking of a genetic syndrome. Zoek ook naar accesoires voor creating conditions the making and remaking of a genetic syndrome. Zo ben je er helemaal klaar voor. Ontdek ook andere producten en koop vandaag nog je creating conditions the making and remaking of a genetic syndrome met korting of in de aanbieding. Alles voor veel leesplezier!
and classification of conditions. Rett Syndrome is thus a key exemplar of the implications of genetic medicine that are far-reaching and;
Vergelijkbare producten zoals Creating Conditions: The making and remaking of a genetic syndrome
and classification of conditions. Rett Syndrome is thus a key exemplar of the implications of genetic medicine that are far-reaching and;
Vergelijkbare producten zoals Creating Conditions
, arrhythmogenic right ventricular cardiomyopathy, and sick sinus syndrome. The issue concludes with a consideration of the potential for genetic testing;
Vergelijkbare producten zoals Genetics Of Cardiac Arrhythmias, An Issue Of Cardiac Electro
. Long QT syndrome may result from a genetic mutation or be caused by certain medications and medical conditions. The condition is treatable with;
Vergelijkbare producten zoals Long QT Syndrome, An Issue of Cardiac Electrophysiology Clinics
Offering a summary of the current state of knowledge in autism research, Defining Autism looks at the different genetic, neurological and;
Vergelijkbare producten zoals Defining Autism
greatly stimulated both theoretical and applied genetic research in recent years. A range of new analytical tools has been developed for the;
Vergelijkbare producten zoals Genetic Endocrinology of the Metabolic Syndrome
be recognized socially, to go to mainstream school, to have a job, to integrate in their community and to enjoy a better quality of life. The;
Vergelijkbare producten zoals Down Syndrome
Chromosomal aberrations are disruptions in the normal chromosomal content of a cell, and are a major cause of genetic conditions in humans;
Vergelijkbare producten zoals Genetic Translocations & Other Chromosome Aberrations
with emphasis on in utero origins and specific genetic and epigenetic factors. This book provides a wealth of relevant information for every;
Vergelijkbare producten zoals Hyperandrogenism in Women
Genetics and Neurobiology of Down Syndrome provides a thorough review of the genetic etiology and mechanisms of trisomy 21. The author;
Vergelijkbare producten zoals Genetics and Neurobiology of Down Syndrome
Down syndrome is a developmental disorder caused by the presence of an extra copy of chromosome 21. This extra genetic material causes;
Vergelijkbare producten zoals Down Syndrome
in every 1000 born in the UK has the condition. Parents are often frightened and confused by the birth of a baby with Down syndrome, and they need;
Vergelijkbare producten zoals Down Syndrome
needs are detected early and effectively managed. This book is the perfect aid for doing so, providing detailed information on the range;
Vergelijkbare producten zoals Medical Aspects of Autism and Asperger Syndrome
There are many disorders of a lack of pigmentation in the skin, with different causations and effects, of which vitiligo is only the;
Vergelijkbare producten zoals Hypopigmentation
This unique, case-based guide provides a thoughtful and comprehensive overview of the genetic basis of male infertility for the practicing;
Vergelijkbare producten zoals Genetics of Male Infertility
for the benefit of everyone. Asperger Syndrome and Employment provides essential information for those making the decisions and;
Vergelijkbare producten zoals Asperger Syndrome and Employment
Prominent researchers and clinicians describe in detail all the latest laboratory techniques currently used to define the molecular genetic;
Vergelijkbare producten zoals Congenital Heart Disease
and some insights on their genetics conservation, systematics and the pleistocene influence on their genetic characteristics; strategies for;
Vergelijkbare producten zoals Advances in Genetics Research
Down syndrome is a condition in which extra genetic material causes delays in the way a child develops, both mentally and physically. It;
Vergelijkbare producten zoals Handbook of Down Syndrome Research
practices reveal, in different ways, the operative role of the photographic media in making and remaking history. Not limited to a particular;
Vergelijkbare producten zoals Lieven Gevaert Series 20 - Images performing history
Rett syndrome, a rare genetic disease caused by mutations of the MECP2 gene, includes severe to profound developmental impairments;
Vergelijkbare producten zoals Rett Syndrome (RTT)
This book provides a fresh, multidisciplinary, and exciting look at the making and remaking of pharmaceutical patents at the GATT/WTO, by;
Vergelijkbare producten zoals the Political Economy of Pharmaceut
This book provides a fresh, multidisciplinary, and exciting look at the making and remaking of pharmaceutical patents at the GATT/WTO, by;
Vergelijkbare producten zoals The Political Economy of Pharmaceutical Patents
, the appetite is often a symptom. This makes our gut a vital indicator of health. Along with the genetic material we inherit the gut microbiota;
Vergelijkbare producten zoals Understanding our Valuable Tenants
> The author here provides basic information about what genetic predispositions, medical conditions, and lifestyle choices make Metabolic;
Vergelijkbare producten zoals Metabolic Syndrome and Psychiatric Illness: Interactions, Pathophysiology, Assessment and Treatment
syndrome, A Scoping Review of Psychosocial Interventions for Neurogenetic Conditions across the Lifespan, Clinical Trials and Outcome Measures;
Vergelijkbare producten zoals Contemporary Issues in Evaluating Treatment in Neurodevelopmental Disorders
Einde inhoud
Geen pagina's meer om te laden'