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To Stay Current With Their Profession, Speechlanguage, And Hearing Clinicians And Students Must Have A Strong Working Knowledge Of Genetic Disorders And Their Associated Symptoms. Dr. Shprintzen'S Comprehensive Manual Provides A Clear, Understandable Overview Of Human Genetics And The Modes Of Inheritance Directly Related To Communicative Disorders, As Well As The Proper Methodology Taking A Detailed Medical, Behavioral, And Genetic History For Diagnosis, Treatment, And Prognosis. Textbook
⚠️ WARNING (California Proposition 65):
This product may contain chemicals known to the State of California to cause cancer,
birth defects, or other reproductive harm.
Q: What is the main focus of 'Genetics, Syndromes and Communication Disorders'?A: The book provides an overview of human genetics and inheritance modes related to communicative disorders, helping clinicians understand genetic disorders and their symptoms.
Q: Who is the author of this textbook?A: The author of the textbook is Dr. Robert J. Shprintzen, who is known for his expertise in genetics and communication disorders.
Q: What edition is this book?A: This is the first edition of 'Genetics, Syndromes and Communication Disorders'.
Q: What type of binding does this book have?A: The book is bound in hardcover, which offers durability and a professional appearance.
Q: How many pages does the book contain?A: The textbook contains 328 pages.
Q: What is the condition of the used book?A: The book is listed as being in good condition, indicating that it has been well maintained.
Q: When was 'Genetics, Syndromes and Communication Disorders' published?A: The book was published on October 1, 1997.
Q: Is this book suitable for students?A: Yes, the book is suitable for speech-language and hearing students, providing essential knowledge on genetic disorders.
Q: What topics are covered in this textbook?A: The textbook covers human genetics, inheritance patterns, diagnosis methods, and the connection between genetic disorders and communication issues.
Q: Can this book assist in clinical practice?A: Yes, the manual offers methodologies for taking detailed medical and genetic histories, which are crucial for diagnosis and treatment in clinical settings.
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