English
- استرجاع مجاني وسهل
- أفضل العروض
Oxford Desk Reference: Clinical Genetics and Genomics
قبل:
د.إ. 1466.00
الآن:
د.إ. 979.00 شامل ضريبة القيمة المضافة
وفرّت:
د.إ. 487.00 د.إ. خصم 33%
توصيل مجاني
باقي 1 وحدات في المخزونتوصيل مجانيباقي 1 وحدات في المخزون
احصل عليه خلال 11 مارس
احصل على د.إ. 48.95 رصيد مسترجع باستخدام بطاقة بنك المشرق نون الائتمانية. اشترك الآن. قدّم الحين
1
توصيل مجاني لنقطة نون ومراكز الاستلام
معرفة المزيد
إرجاع سهل لكل المنتجات في هذا العرض.
الميزات الأساسية
- Oxford University Press
- Firth, Helen V. (Consultant in Clinical Genetics, Consultant in Clinical Genetics, Cambridge Univers
- Oxford Desk Reference: Clinical Genetics and Genomics
المواصفات
| الناشر | Oxford University Press |
| رقم الكتاب المعياري الدولي 13 | 9780199557509 |
| رقم الكتاب المعياري الدولي 10 | 199557500 |
| الكاتب | Firth, Helen V. (Consultant in Clinical Genetics, Consultant in Clinical Genetics, Cambridge Univers |
| تنسيق الكتاب | Hardcover |
| اللغة | English |
| وصف الكتاب | Oxford Desk Reference: Clinical Genetics and Genomics |
| عن المؤلف | Dr Helen Firth, DM FRCP DCH is a Consultant Clinical Geneticist at Cambridge University Hospitals, an Honorary Faculty Member of the Wellcome Trust Sanger Institute, and a Bye-Fellow of Newnham College, Cambridge. Her main research interests are in mapping the clinical genome and the matching of rare genomic variants to empower discovery and diagnosis in rare disease. In 2004, she initiated the DECIPHER project ( that enables clinicians and scientists around the world to share information about rare genomic variants to facilitate diagnosis and help to elucidate the role of genes whose function is not yet known. In 2010 Dr Firth became Clinical Lead for the Deciphering Developmental Disorders study (DDD study) ( one of the world's largest nationwide, genome-wide sequencing projects in rare disease. The study aims to improve diagnosis and further understanding of the genomic architecture of severe developmental disorders. Dr Jane Hurst is a clinician working full time as a clinical geneticist in the one of the leading children's hospitals in the world; a centre of excellence for the diagnosis and treatment of rare diseases. She moved to her current post in 2010 to lead the dysmorphology service after 18 years working in Oxford, UK. Although primarily a patient-focussed clinician, she has always worked closely with scientific colleagues by identifying families that give important clues to the genetic aetiology. Thus early in her career she identified the first family shown to have leptin deficiency and the two families that led to the cloning of the FOXP2 gene. |
| تقييم الآباء | 12+ |
| Language | English |
| تاريخ النشر | 2017 |
| عدد الصفحات | 936.0 |
Oxford Desk Reference: Clinical Genetics and Genomics
تمت الإضافة لعربة التسوق
مجموع السلة 979.00 د.إ.
