دانلود کتاب سندروم های سروگردنSyndromes of the Head and Neck 4 ED (کد: RXN1080)

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کتاب سندروم های سروگردنSyndromes of the Head and Neck (Oxford Monographs on Medical Genetics) 4th Editionویرایش چهارم 2001 :

کتاب دکر شده با فرمت پی دی اف بوده و قابلیت اجرا بر روی تمامی دیوایس های پشتیبان کننده از PDF را دارا می باشد.

کتاب ارائه شده توسط با ضمانت و صد در صد اورجینال و شامل 1328صفحه می باشد و تفاوت آن با نسخه های متفرقه، در کیفیت تصاویر و متون کتاب وهمچنین امکان هایلایت و کپی برداری ساده از متون و تصاویر موجود در کتاب می باشد که همین امر سبب تفاوت رنج قیمت گردیده بطوریکه قیمت کتاب سندروم های سروگردنSyndromes of the Head and Neck (Oxford Monographs on Medical Genetics) 4th Editionویرایش چهارم 2001 در سایت اصلی و سایت های فروش خارجی بین 50 الی 65 دلار میباشد.

978-0195118612,ISBN:0195118618 

حجم فایل:68MB

نویسندگان :Robert J. Gorlin , M. Michael Cohen, Raoul C.M. Hennekam


توضیحات تکمیلی:

  • This classic text, one of the true anchors of our clinical genetics publishing program, covers over 700 different genetic syndromes involving the head and neck, and it has established itself as the definitive, comprehensive work on the subject. The discussion covers the phenotype spectrum, epidemiology, mode of inheritance, pathogenesis, and clinical profile of each condition, all of which is accompanied by a wealth of illustrations. The authors are recognized leaders in the field, and their vast knowledge and strong clinical judgment will help readers make sense of this complex and burgeoning field.

    Dr. Gorlin retires as editor in this edition and co-editor Raoul Hennekam takes over. Dr. Hennekam is regarded as one of the top dysmorphologists--and indeed one of the top clinical geneticists--in the world. Judith Allanson is new to the book but is a veteran OUP author and a widely respected geneticist, and Ian Krantz at Penn is a rising star in the field. Dr. Gorlin's name has always been closely associated with the book, and it has now become part of the title.

    As in all fields of genetics, there has been an explosion in the genetics of dysmorphology syndromes, and the author has undertaken a complete updating of all chapters in light of the discoveries of the Human Genome Project and other ongoing advances, with some chapters requiring complete rewriting. Additional material has been added both in terms of new syndromes and in updating information on existing syndromes. The book will appeal to clinical geneticists, pediatricians, neurologists, head and neck surgeons, otolarynologists, and dentists. The 4th edition, which published in 2001, has sold 2,600 copies.
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