Chromosomal Syndromes
Autor Pai, Borgaonkar, Lewandowskien Limba Engleză Hardback – 28 oct 2002
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Specificații
ISBN-13: 9780471372172
ISBN-10: 047137217X
Pagini: 376
Dimensiuni: 183 x 260 x 25 mm
Greutate: 0.9 kg
Editura: Wiley
Locul publicării:Hoboken, United States
ISBN-10: 047137217X
Pagini: 376
Dimensiuni: 183 x 260 x 25 mm
Greutate: 0.9 kg
Editura: Wiley
Locul publicării:Hoboken, United States
Public țintă
Human Geneticists, Human Medical Cytogeneticists, Genetic Counselors, Primary Medical Care Providers, Health Care Professionals, Teachers and Educators in Health and Biological SciencesNotă biografică
Dr. Digamber S. Borgaonkar obtained his Ph.D. degree in genetics from Oklahoma State University. He joined the Division of Medical Genetics at Johns Hopkins University School of Medicine as Director of the Chromosome Laboratory in 1964. Dr. Borgaonkar initiated the Chromosomal Variation in Man database www.wiley.com/borgaonkar at Johns Hopkins in 1974. He was later appointed human medical geneticist for the State of Delaware.
Dr. G. Shashindhar Pai has been an active teacher, practitioner and researcher of clinical genetics for more than 25 years. The author of nearly 100 papers relating to clinical genetics and cytogenetics, Dr. Pai currently serves on the faculty of the Division of Genetics at the Medical University of South Carolina.
Dr. Raymond Lewandowski is at the Center for Genetic Services in Corpus Christi, Texas.
Dr. G. Shashindhar Pai has been an active teacher, practitioner and researcher of clinical genetics for more than 25 years. The author of nearly 100 papers relating to clinical genetics and cytogenetics, Dr. Pai currently serves on the faculty of the Division of Genetics at the Medical University of South Carolina.
Dr. Raymond Lewandowski is at the Center for Genetic Services in Corpus Christi, Texas.
Descriere
This comprehensive reference provides a pictorial and descriptive account of approximately 200 chromosomal aneuploidy syndromes. It focuses exclusively on clinical syndromes due to chromosomal abnormalities.