Human Malformations and Related Anomalies: Oxford Monographs on Medical Genetics, cartea No. 52
Editat de Roger E. Stevenson, Judith G. Hallen Limba Engleză Hardback – 30 noi 2005
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Specificații
ISBN-13: 9780195165685
ISBN-10: 0195165683
Pagini: 1520
Ilustrații: 653 black & white photographs,176 line illustrations, numerous tables
Dimensiuni: 225 x 287 x 60 mm
Greutate: 3.62 kg
Ediția:2
Editura: Oxford University Press
Colecția OUP USA
Seria Oxford Monographs on Medical Genetics
Locul publicării:New York, United States
ISBN-10: 0195165683
Pagini: 1520
Ilustrații: 653 black & white photographs,176 line illustrations, numerous tables
Dimensiuni: 225 x 287 x 60 mm
Greutate: 3.62 kg
Ediția:2
Editura: Oxford University Press
Colecția OUP USA
Seria Oxford Monographs on Medical Genetics
Locul publicării:New York, United States
Recenzii
From reviews of the first edition:
Provides an excellent, up-to-date summary that is an important resource for any clinical geneticist... The chapters are well-illustrated and include lists of associated syndromes that can be used to narrow down a diagnosis for a patient, or provide a broad review that is useful for medical rounds. This set is well worth the investment.
I am pleased to say that... 'field trials' have confirmed without doubt the excellence of this huge and scholarly work. It will be a key reference text for students, researchers, biomedical scientists, and clinicians, particularly clinical geneticists, paediatricians, and obstetricians. Extensive and up to date references are given and the vast number of illustrations and line diagrams are excellent... The editors are to be congratulated on their concept and design of thesevolumes... I really don't have any criticisms... I would strongly recommend that this book is used as a 'bench book' and is located in all clinical genetics departments; the hospital or university library should also contain a reference copy.
Provides an excellent, up-to-date summary that is an important resource for any clinical geneticist... The chapters are well-illustrated and include lists of associated syndromes that can be used to narrow down a diagnosis for a patient, or provide a broad review that is useful for medical rounds. This set is well worth the investment.
I am pleased to say that... 'field trials' have confirmed without doubt the excellence of this huge and scholarly work. It will be a key reference text for students, researchers, biomedical scientists, and clinicians, particularly clinical geneticists, paediatricians, and obstetricians. Extensive and up to date references are given and the vast number of illustrations and line diagrams are excellent... The editors are to be congratulated on their concept and design of thesevolumes... I really don't have any criticisms... I would strongly recommend that this book is used as a 'bench book' and is located in all clinical genetics departments; the hospital or university library should also contain a reference copy.