Genetic Diseases And Development Disabilities: Aspects Of Detection And Prevention
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A01=Tamah L Sadick
Abruptio Placenta
Age Group_Uncategorized
Age Group_Uncategorized
Alpha-1 Antitrypsin Deficiency
Author_Tamah L Sadick
automatic-update
carrier screening
Carrier Test
Category1=Non-Fiction
Category=JHB
chromosomal disorders
CMV Infection
COP=United Kingdom
CPK Level
Delivery_Pre-order
developmental disabilities
Dried Blood Spot Specimen
Duchenne Muscular Dystrophy
Elevated CPK Level
eq_bestseller
eq_isMigrated=2
eq_nobargain
eq_non-fiction
eq_society-politics
Fetal Blood Sampling
Fetal Red Cell
genetic disorders
genetic screening protocols in healthcare
heterozygote detection
homozygote newborn screening
Language_English
Lung Function Analysis
Maple Syrup Urine Disease
Maternal Serum Afp Screening
medical genetics
neural tube defect detection
NICHD Study
PA=Temporarily unavailable
prenatal diagnosis
prenatal diagnostic techniques
Price_€20 to €50
Probability Density Function Method
PS=Active
Severe Alpha-1 Antitrypsin Deficiency
softlaunch
Spina Bifida
White Blood Cells
White Cell
X-linked disease counseling
Product details
- ISBN 9780367168162
- Weight: 280g
- Dimensions: 144 x 229mm
- Publication Date: 26 Oct 2020
- Publisher: Taylor & Francis Ltd
- Publication City/Country: GB
- Product Form: Paperback
- Language: English
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This book emphasizes the application of new developments in medical genetics to real-life situations. It includes reviews on homozygote new born screening, heterozygote detection in the community, and prenatal diagnostic techniques such as ultrasonography, amniocentesis, and fetal blood sampling.
