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Signs and Symptoms of Genetic Conditions: A Handbook
By Helga V. Toriello (editor), Louanne Hudgins (editor), Gregory M. Enns (editor) and H. Eugene Hoyme (editor)
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Bibliographic Detail
Publisher Oxford Univ Pr
Publication date June 27, 2014
Pages 540
Binding Paperback
Edition 1
Book category Adult Non-Fiction
ISBN-13 9780199930975
ISBN-10 019993097X
Dimensions 1 by 6.50 by 9.25 in.
Weight 1.70 lbs.
Original list price $84.00
Summaries and Reviews
Amazon.com description: Product Description: Connecting an abnormal physical exam to a possible genetic condition is a daunting and inexact task for any physician, be they a primary care provider, non-geneticist specialist, or fellowship-trained geneticist.

Comprising 31 clinical protocols from the world's foremost clinical geneticists, Signs and Symptoms of Genetic Conditions provides a practical manual for the diagnosis and management of common human genetic conditions based on their presenting signs and/or symptoms. Each chapter examines a specific clinical finding and leads the user through a step-by-step approach to a differential diagnosis.

To maximize clinical utility, this handbook features:

· Prominent flow chart diagrams that graphically depict the diagnostic approach
· Concise recommendations for laboratory and/or imaging studies
· Health supervision and management strategies for the most common conditions associated with each presenting sign or symptom

Whether for the student, resident, or seasoned clinician, Signs and Symptoms of Genetic Conditions will serve as a frontline resource for navigating differential diagnosis.


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Paperback
Book cover for 9780199930975
 
The price comparison is for this edition
With Gregory M. Enns (other contributor), Helga V. Toriello (other contributor), Louanne Hudgins (other contributor) | 1 edition from Oxford Univ Pr (June 27, 2014)
9780199930975 | details & prices | 540 pages | 6.50 × 9.25 × 1.00 in. | 1.70 lbs | List price $84.00
About: Connecting an abnormal physical exam to a possible genetic condition is a daunting and inexact task for any physician, be they a primary care provider, non-geneticist specialist, or fellowship-trained geneticist.

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