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Genetic Consultations in the Newborn

93.35
88.68
The definitive work in genetic evaluation of newborns. I cannot recommend it strongly enough." -Judith G. Hall

As demand continues to exceed availability when it comes to clinical geneticists, Genetic Consultations in the Newborn offers an essential new resource for practitioners everywhere: a streamlined diagnostic manual that connects subtle symptoms of newborn dysmorphology to their differential diagnosis.

Comprising more than 60 chapters organized by system and symptom, this book facilitates fast, expert navigation from recognition to management in syndromes that manifest during the newborn period. Richly illustrated and packed with pearls of practical wisdom from the authors' decades of practice, it empowers readers to recognize the outward signs and symptoms crucial for an effective diagnosis.

For geneticists, neonatologists, pediatricians, and anyone else who cares for infants in their first days of life, Genetic Consultations in the Newborn provides an essential and unmatched resource for navigating one of the most challenging areas of clinical practice. It should not be missed.

A streamlined diagnostic manual for neonatologists, clinical geneticists, and pediatricians - any clinician who cares for newborns
Organized by symptom and system, enriched with more than 250 photographs and clinical pearls derived from the authors' decades of clinical practice
Includes "Syndromes You Should Know" appendix, distilling the most frequently encountered syndromes and chromosomal abnormalities in newborns
OMIM numbers for each condition situate authors' practical guidance in the broader genetics literature, connecting readers to the most up-to-date references
An essential resource for all who care for infants during their first moments of life
Robin D. Clark, MD, is Professor of Pediatrics in the Division of Medical Genetics at Loma Linda School of Medicine. She has more than 30 years' experience in the practice of clinical genetics, including expertise in dysmorphology, prenatal diagnosis, cytogenetics, and clinical cancer genetics. She trained in medical genetics at Harbor-UCLA Medical Center and in dysmorphology at the Institute for Child Health in London. Cynthia J. Curry, MD, is Professor of Pediatrics, Emerita, at the University of California, San Francisco. She is an accomplished dysmorphologist and clinical geneticist with decades of experience in the evaluation of infants and children with both common and rare problems and malformations. She is an expert on the prenatal evaluation of abnormal fetal presentations and of stillborn infants. She developed the genetic services at Valley Children's Hospital in Madera, California, and at Community Regional Medical Center in Fresno, California.
Autores
ISBN
978-0-19-999099-3
EAN
9780199990993
Editor
Oxford University Press
Stock
NO
Idioma
Inglés
Nivel
Profesional
Formato
Encuadernado
Rústica
Páginas
400
Largo
290
Ancho
220
Peso
-
Edición
Fecha de edición
23-03-2019
Año de edición
2019
Nº de ediciones
1
Colección
-
Nº de colección
-