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Chromosome Abnormalities and Genetic Counseling (Oxford Monographs on Medical Genetics) de Grant R Sutherland
Descripción - Críticas Review(s) from other edition(s)As one who has watched human cytogenetics from its birth in 1956 to its present extraordinary capabilities and who counsels families with chromosomal problems without ever having learned how to prepare a karyotype, I found this book a godsend...The writing is rigorous and often elegant. Gardner and Sutherland have the necessary knowledge to and provide useful assessments of the available information. (New England Journal of Medicine)Chromosome Abnormalities and Genetic Counseling is a comprehensive text encompassing a full complement of cytogenetic information. Concepts are introduced such as basic cytogenetic elements, ethical and counseling issues and the handling of risk figures. A brief and concise review of chromosome pathology is included, enough to refresh the memory without insulting the reader's intelligence...This book is a wonderful asset to any library and can serve either as an educational text or as a reference. (Applied Cytogentics)...this book has been written primarily for two groups of readers: the genetic counsellor (both medical and nonmedical) and the cytogenetic laboratory scientist. There are substantial sections of the book, however, which are of relevance to paediatricians...The authors are to be congratulated, not only because their book is one of the best of its kind, written in a clear and balanced manner and practically oriented! (Journal of Paediatrics and Child Health) Reseña del editor Chromosome abnormalities have been known for over 50 years, though the methods of analysis have become increasing more sophisticated and precise. Surprisingly, the questions that parents and families raise in genetic counseling have changed little over that period. Questions like, 'Why did an abnormality happen? Why did it cause the problems we see in our child? Would it happen again in a future child? How could we avoid it happening again?' are common concerns for families. This new edition of Chromosome Abnormalities and Genetic Counseling deals with these universal questions, and in the context of the recent developments in molecular cytogenetic analysis, but retaining always the major focus on the needs of the families in which these conditions occur. Thoroughly updated once again, this richly-illustrated text combines basic concepts of chromosomal analysis with practical applications of recent advances in molecular cytogentics. The book will give counselors the information that will enable them to help concerned parents accommodate and adapt to their particular chromosomal challenges and to determine what may be, for them, the best course of action. Biografía del autor Lisa G. Shaffer is President of Signature Genomic Laboratories. R.J. McKinlay Gardner is a Consultant Medical Geneticist at Northern Regional Genetic Service at Auckland City Hospital. Grant R. Sutherland is an Emeritus Geneticist at Women's and Children's Hospital in Adelaide, Australia.
Detalles del Libro
- Name: Chromosome Abnormalities and Genetic Counseling (Oxford Monographs on Medical Genetics)
- Autor: Grant R Sutherland
- Categoria: Libros,Libros universitarios y de estudios superiores,Medicina y ciencias de la salud
- Tamaño del archivo: 11 MB
- Tipos de archivo: PDF Document
- Descargada: 714 times
- Idioma: Español
- Archivos de estado: AVAILABLE
Download Chromosome Abnormalities and Genetic Counseling (Oxford Monographs on Medical Genetics) de Grant R Sutherland PDF [ePub Mobi] Gratis
Chromosome Abnormalities and Genetic Counseling (Oxford ~ Chromosome Abnormalities and Genetic Counseling (Oxford Monographs on Medical Genetics Book 61) (English Edition) eBook: McKinlay Gardner, R.J.M, Sutherland, Grant R, Shaffer, Lisa G.: : Tienda Kindle
Chromosome Abnormalities and Genetic Counseling - Oxford ~ This new edition of Chromosome Abnormalities and Genetic Counseling is a thoroughly updated ands richly-illustrated resource, combining basic concepts of chromosomal analysis with practical applications of recent advances in molecular cytogentics. It gives counselors the information that will enable them to help concerned parents accommodate and adapt to their particular chromosomal challenges .
Chromosome Abnormalities and Genetic Counseling - R.J.M ~ Chromosome abnormalities have been known for over 50 years, though the methods of analysis have become increasing more sophisticated and precise. Surprisingly, the questions that parents and families raise in genetic counseling have changed little over that period.
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Chromosome Abnormalities - Oxford Medicine ~ This chapter covers the following chromosome abnormalities: TRISOMY 21, TRISOMY 18, TRISOMY 13, and includes definitions, appearance, associated malformations, developmental defect, prevalence, genetic factors, environmental factors, treatment and prognosis, and genetic counselling.
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Chromosome Abnormalities and Genetic Counseling - R.J ~ Chromosome abnormalities have been known for over 50 years, though the methods of analysis have become increasing more sophisticated and precise. Surprisingly, the questions that parents and families raise in genetic counseling have changed little over that period. Questions like, "Why did an abnormality happen? Why did it cause the problems we see in our child?
Clinical Genetics - Oxford University Press ~ Chromosome Abnormalities and Genetic Counseling. Fourth Edition. R.J.M Gardner, Grant R Sutherland, and Lisa G. Shaffer . Online Resource Oxford Monographs on Medical Genetics. Chromosome Segregation & Structure. Cold Spring Harbor Symposium on Quantitative Biology, Volume LXXXII $
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Medical Genetics: How Chromosome Abnormalities Happen ~ Medical Genetics: How Chromosome Abnormalities Happen. Chromosomes are stick-shaped structures in the middle of each cell in the body. Each cell has 46 chromosomes grouped in 23 pairs.
Genetic counseling for sex chromosome abnormalities ~ Sex chromosome abnormalities (SCAs) are the most frequently occurring chromosomal abnormalities encountered at both prenatal diagnosis and at birth. Approximately 1/400 newborns has an SCA, and incidence at prenatal diagnosis is even greater, 1/250 to 1/300.
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