Genetic Diseases And Development Disabilities: Aspects Of Detection And Prevention
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A01=Tamah L Sadick
Abruptio Placenta
Alpha-1 Antitrypsin Deficiency
Author_Tamah L Sadick
carrier screening
Carrier Test
Category=JHB
chromosomal disorders
CMV Infection
CPK Level
developmental disabilities
Dried Blood Spot Specimen
Duchenne Muscular Dystrophy
Elevated CPK Level
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Fetal Blood Sampling
Fetal Red Cell
genetic disorders
genetic screening protocols in healthcare
heterozygote detection
homozygote newborn screening
Lung Function Analysis
Maple Syrup Urine Disease
Maternal Serum Afp Screening
medical genetics
neural tube defect detection
NICHD Study
prenatal diagnosis
prenatal diagnostic techniques
Probability Density Function Method
Severe Alpha-1 Antitrypsin Deficiency
Spina Bifida
White Blood Cells
White Cell
X-linked disease counseling
Product details
- ISBN 9780367018290
- Weight: 440g
- Dimensions: 144 x 229mm
- Publication Date: 25 Apr 2019
- Publisher: Taylor & Francis Ltd
- Publication City/Country: GB
- Product Form: Hardback
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Advances in medical genetics during the past two decades have made possible the detection and prevention of many genetic disorders and developmental disabilities. The emphasis of this book is on the application of these new developments to real-life situations. Covering homozygote newborn screening, heterozygote detection in the community, and pren
