Oxford Desk Reference: Clinical Genetics and Genomics
9780199557509
-
₪545.00₪604.00
פריט זה ניתן על ידי קרדיטים.
לחצו על "הוספה לעגלה" להמשך
לחצו על "הוספה לעגלה" להמשך
אזל המלאי עבור /
-
זמן אספקה ותנאי רכישההערות:
• זמן אספקה: הזמנות בהן כל הספרים זמינים במלאי - זמן אספקה – כ- 5 ימי עסקים (למעט אזורים חריגים בהם ייתכן עיכוב נוסף).
ספרים שאינם זמינים במלאי: זמן אספקה כ- 14 -45 ימי עסקים בהתאם למלאי במחסני המו"ל בחו"ל - הודעה תימסר ללקוח.
• הזמנה במשקל כולל של עד 14 קילו ישלחו ללקוח באמצעות חברת שליחויות עם שליח עד הבית (בישובים מסוימים המסירה תתבצע למרכז חלוקת הדואר המקומי)
• במידה וקיים עיכוב במשלוח ההזמנה או חוסר במלאי הספרים תשלח הודעה ללקוח.
• במידה ויבחר הלקוח עקב עיכוב במשלוח כנ"ל לבטל הזמנתו ויודיע על כך לידע, ידע מתחייבת לזכות החיוב.
• במידה ויתברר כי הספרים אזלו מהמלאי ולא ניתן לספקם - תשלח הודעה ללקוח.
• האיסוף העצמי ממשרדי ידע יבוצע רק לאחר הודעה ללקוח שההזמנה מוכנה לאיסוף.
דמי משלוח:
ניתן לבחור: 1. איסוף עצמי - ללא תשלום
2. משלוח עד הבית
Oxford Desk Reference: Clinical Genetics and Genomics/ Helen V. Firth ,Jane A. Hurst
2nd Edition
A popular and easy-to-use guide, this book is a must-have tool for clinical consultations in genetics and genomic medicine.
Ideal for quick reference during practice, it covers the process of diagnosis, investigation, management, and counselling for patients. With a strong evidence base and international guidelines, it puts reliable and trustworthy guidance at your fingertips. Designed for use as a first-line guide, the A to Z format ensures it's accessible, and the simple layout makes it easy to assimilate information. Highly illustrated, the book also contains up-to-date glossaries of terms used in genetics and
dysmorphology providing quick reference for key concepts.
The second edition is an eagerly anticipated update of the gold standard in the specialty. It covers new developments in the field, particularly the advent of genome-wide sequencing and major updates in cancer. Fifteen new topics have been added, including Sudden cardiac death, Neonatal screening, and Ciliopathies.
The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both outpatient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered, and where available diagnostic criteria are included. In addition there are chapters on familial cancer and pregnancy-related topics such as fetal anomalies, teratogens, prenatal and pre-implantation diagnosis and non-invasive prenatal
testing. The book also provides information on the less common situations where management is particularly complex.
Both practical and pertinent, Oxford Desk Reference: Clinical Genetics and Genomics is the companion you need by your side during clinical consultations.
A popular and easy-to-use guide, this book is a must-have tool for clinical consultations in genetics and genomic medicine.
Ideal for quick reference during practice, it covers the process of diagnosis, investigation, management, and counselling for patients. With a strong evidence base and international guidelines, it puts reliable and trustworthy guidance at your fingertips. Designed for use as a first-line guide, the A to Z format ensures it's accessible, and the simple layout makes it easy to assimilate information. Highly illustrated, the book also contains up-to-date glossaries of terms used in genetics and
dysmorphology providing quick reference for key concepts.
The second edition is an eagerly anticipated update of the gold standard in the specialty. It covers new developments in the field, particularly the advent of genome-wide sequencing and major updates in cancer. Fifteen new topics have been added, including Sudden cardiac death, Neonatal screening, and Ciliopathies.
The authors have used their experience to devise a practical clinical approach to many common genetic referrals, both outpatient and ward based. The most common Mendelian disorders, chromosomal disorders, congenital anomalies and syndromes are all covered, and where available diagnostic criteria are included. In addition there are chapters on familial cancer and pregnancy-related topics such as fetal anomalies, teratogens, prenatal and pre-implantation diagnosis and non-invasive prenatal
testing. The book also provides information on the less common situations where management is particularly complex.
Both practical and pertinent, Oxford Desk Reference: Clinical Genetics and Genomics is the companion you need by your side during clinical consultations.
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