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Genetic Disorders and the Fetus: Diagnosis, Prevention, and Treatment [Hardcover]

Dr. Aubrey Milunsky MBBCh DSc FRCP FACMG DCH (Editor)


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Book Description

April 21, 2004 0801879280 978-0801879289 5th

The definitive reference work on prenatal diagnosis, Genetic Disorders and the Fetus is now available in a completely revised and updated fifth edition reflecting the most current advances in research, technology, and clinical care.

Written by an international team of experts, the volume provides an in-depth critical analysis and synthesis of the latest work in prenatal diagnosis of genetic disorders and fetal malformations. This volume represents a substantial repository of facts and emphasizes important advances in the prenatal detection and screening for cystic fibrosis, neural tube defects, chromosomal abnormalities, hemoglobinopathies, and fragile X syndrome. Technical advances in fetal blood sampling, abortion, and fetal therapy are highlighted, and an enormous personal experience with chorionic villus sampling provides valuable lessons and guidance. The extensive compilation of information concerning the prenatal detection of chromosomal abnormalities is essential to all those engaged daily in prenatal genetic diagnosis.

Other topics include: multianalyte screening for neural tube and chromosomal defects, with special reference to the first-trimester screening; fetal imaging; advances in molecular genetics that facilitate prenatal diagnosis and the indications, limitations, pitfalls, and guidelines for this type of testing; and the prenatal diagnosis of lipid, mucopolysaccharide, amino acid, folate, and other metabolic disorders, congenital adrenal hyperplasia, and immunodeficiency disorders. A comprehensive review and synthesis of the medicolegal and ethical aspects of prenatal genetic diagnosis completes this heavily referenced, up-to-date volume.

Table of Contents

1 Genetic Counseling: Preconception, Prenatal, and Perinatal / Aubrey Milunsky and Jeff M. Milunsky 2 Amniocentesis and Fetal Blood Sampling / Sherman Elias and Joe Leigh Simpson 3 Amniotic Fluid / Louis Dallaire and Aubrey Milunsky 4 Amniotic Fluid Cell Culture / Daniel L. Van Dyke 5 Prenatal Genetic Diagnosis through Chorionic Villus Sampling / Bruno Brambati and Lucia Tului 6 Prenatal Diagnosis of Chromosomal Abnormalities through Amniocentesis / Peter A. Benn and Lillian Y. F. Hsu 7 Prenatal Diagnosis of Sex Chromosome Abnormalities / Jeff M. Milunsky 8 Molecular Cytogenetics and Prenatal Diagnosis / Stuart Schwartz 9 Prenatal Diagnosis of the Fragile X Syndrom / Edmund C. Jenkins and W. Ted Brown 10 Molecular Genetics and Prenatal Diagnosis / Thomas W. Prior, Aubrey Milunsky, Cindy L. Vnencak-Jones, and John A. Phillips III 11 Prenatal Diagnosis of Disorders of Lipid Metabolism / Bryan G. Winchester and Elisabeth P. Young 12 Prenatal Diagnosis of Disorders of Mucopolysaccharide Metabolism / Gideon Bach 13 Disorders of the Metabolism of Amino Acids and Related Compounds / Vivian E. Shih and Roseann Mandell 14 Prenatal Diagnosis of Disorders of Carbohydrate Metabolism / Yuan-Tsong Chen 15 Prenatal Diagnosis of Cystic Fibrosis / Gerald L. Feldman and Kristin G. Monaghan 16 Prenatal Diagnosis and Treatment of Congenital Adrenal Hyperplasia / Phyllis W. Speiser 17 Prenatal Diagnosis of Miscellaneous Biochemical Disorders / David S. Rosenblatt 18 Prenatal Diagnosis of Primary Immunodeficiency Diseases / Jennifer M. Puck 19 Prenatal Diagnosis of the Hemoglobinopathies / John M. Old 20 Prenatal Diagnosis of Connective Tissue Disorders / James C. Hyland and Leena Ala-Kokko 21 Maternal Serum Screening for Neural Tube and Other Defects / Aubrey Milunsky and Jacob A. Canick 22 Multimarker Maternal Serum Screening for Chromosomal Abnormalities / Howard S. Cuckle and Svetlana Arbuzova 23 Prenatal Diagnosis of Fetal Malformations by Ultrasound / Yves G. Ville, Kypros H. Nicolaides, and Stuart Campbell 24 Prenatal Diagnosis and Management of Abnormal Fetal Development in the Third Trimester of Pregnancy / J. W. Wladimiroff 25 Prenatal Magnetic Resonance Imaging for Fetal Abnormalities / Anne M. Hubbard 26 Induced Abortion for Genetic Indications: Techniques and Complications / Lee P. Shulman, Sherman Elias, and Joe Leigh Simpson 27 Preimplantation Genetic Diagnosis / Yury Verlinsky and Anver Kuliev 28 Prenatal Diagnosis through the Analysis of Fetal Cells and Cell-Free Nucleic Acids in the Maternal Circulation / Diana W. Bianchi 29 Fetal Therapy / Diana L. Farmer, Hanmin Lee, Michael R. Harrison, and Kerilyn K. Nobuhara 30 Prenatal Diagnosis of Fetal Infection / Fernand Daffos, Fran& ccedil;ios Jacquemard, V& eacute;ronique Mirlesse, St& eacute;phane Romand, and Philippe Thulliez 31 Medicolegal Aspects of Prenatal Diagnosis / Mary Z. Pelias 32 Ethical Issues in the Diagnosis and Management of Genetic Disorders in the Fetus / Frank A. Chervenak and Laurence B. McCullough Appendix: Prenatal Diagnosis of Additional Miscellaneous Genetic Disorders / Aubrey Milunsky


Editorial Reviews

From The New England Journal of Medicine

For several years, Genetic Disorders and the Fetus has belonged with the classic textbooks on the shelf of every geneticist involved in genetic medicine. Because the book approaches each topic in depth, it is an invaluable reference not only for physicians but also for scientists interested in human fetal development. Topics range from the prenatal diagnosis and screening of chromosomal, biochemical, and multifactorial disorders to preimplantation genetic diagnosis and noninvasive prenatal diagnostic methods that involve the analysis of fetal cells and cell-free nucleic acids in the maternal circulation. The outstanding chapters on genetic counseling, chromosomal disorders and their detection through the screening of maternal serum, and molecular cytogenetic methods form the core of this well-designed book. The attention given particularly to the predictive prenatal diagnosis of severe adult-onset genetic disorders, to issues raised by the use of early amniocentesis, and to the recent recognition of the late-onset tremor-ataxia syndrome in male carriers of the fragile X syndrome bring the book up to date. Finally, by including a chapter on fetal infection, the author extends the coverage of topics to nongenetic disorders. In editing the fifth edition of this multiauthored book, Milunsky has succeeded in providing an updated source of guidance and a major repository of knowledge for those of us practicing fetal medicine and involved in human fetal research. Michel Vekemans, M.D., Ph.D.
Copyright © 2005 Massachusetts Medical Society. All rights reserved. The New England Journal of Medicine is a registered trademark of the MMS.

Review

"For several years, Genetic Disorders and the Fetus has belonged with the classic textbooks on the shelf of every geneticist involved with genetic medicine... In editing the fifth edition of this multiauthored book, Milunsky has succeeded in providing an updated source of guidance and a major repository of knowledge for those of us practicing fetal medicine and involved in human fetal research." -- New England Journal of Medicine



"Each clinical genetics and obstetric unit should have a copy of this volume to hand, as it remains the textbook on genetic disorders that may present in pregnant patients and their relatives." -- John L Tolmie, Human Genetics



"The extensive compilation of information concentrating the prenatal detection of chromosomal abnormalities is essential to all those engaged in prenatal genetic diagnosis." -- New Medical World Weekly


Product Details

  • Hardcover: 1248 pages
  • Publisher: The Johns Hopkins University Press; 5th edition (April 21, 2004)
  • Language: English
  • ISBN-10: 0801879280
  • ISBN-13: 978-0801879289
  • Product Dimensions: 10.3 x 7.2 x 2.5 inches
  • Shipping Weight: 5.1 pounds
  • Amazon Best Sellers Rank: #2,819,791 in Books (See Top 100 in Books)

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Inside This Book (learn more)
First Sentence:
Sequencing of the human genome has spawned much hope in the hearts and minds of millions affected by genetic disorders and their loved ones. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
churionic villus, venous volume flow, carhoxylase deficiency, cystic fihrusis, maternal hysterotomy, noncultivated cells, curved arrowhead, trisomie cells, specific mutation detection, fetal patient, prenatal cytogenetic diagnosis, prenatal genetic studies, molecular hases, antniotic fluid, scrum screening, supernumerary marker chromosomes, cytogenetic confirmation, spina hitida, open spina hifida, concurrent screening, maternal cell contamination, prenatal diagnostic studies, gene transfer research, hydratase deficiency, fetal sacrococcygeal teratoma
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Prenat Diagn, Med Genet, Obstet Gynecol, Hum Genet, New York, Ohstet Gynecol, Nat Genet, Inherit Metab Dis, Obstet Gynaecol, Clin Genet, Acad Sci, Inherit Metah Dis, Pediatr Res, Hum Mol Genet, Hum Reprod, Pediatr Surg, Mcd Genet, Ultrasound Med, Clin Invest, Fetal Diagn Ther, Hum Mutat, Ohstet Gynecul, Clin Endocrinol Metab, Ohstet Gynaecol, Plenum Press
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