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Genetics Metabolic & Syndromes

Craniosynostosis and Rare Craniofacial Clefts: Diagnosis, Treatment, and Outcomes 1st Edition 2016

Craniosynostosis and Rare Craniofacial Clefts: Diagnosis, Treatment, and Outcomes 1st Edition 2016

Craniosynostosis and Rare Craniofacial Clefts: Diagnosis, Treatment, and Outcomes 1st Edition 2016 Craniosynostosis and Rare Craniofacial Clefts: Diagnosis, Treatment, and Outcomes 1st Edition 2016  (New Developments in Medical Research) Craniosynostosis and rare craniofacial clefts represent overlapping spectra of craniofacial disorders that present significant multi-system challenges in reconstructive surgery. Caused by …

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Down’s Syndrome Screening and Reproductive Politics 1st Edition 2017

Down's Syndrome Screening and Reproductive Politics 1st Edition 2017

Down’s Syndrome Screening and Reproductive Politics 1st Edition 2017 Down’s Syndrome Screening and Reproductive Politics 1st Edition 2017 Down’s Syndrome Screening and Reproductive Politics: Care, Choice, and Disability in the Prenatal Clinic (Routledge Studies in the Sociology of Health and Illness) 1st Edition 2017 In the UK and beyond, Down’s syndrome …

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Cleft Lip and Palate Management: A Comprehensive Atlas 1st Edition 2015

Cleft Lip and Palate Management: A Comprehensive Atlas 1st Edition 2015

Cleft Lip and Palate Management: A Comprehensive Atlas 1st Edition 2015 Cleft Lip and Palate Management: A Comprehensive Atlas 1st Edition 2015 Cleft Lip and Palate Management: A Comprehensive Atlas—with more than 400 photographs and illustrations—provides the latest concepts about the surgical/orthodontic interrelation in cleft lip and palate treatment. Dr. …

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Succinct Pediatrics: Evaluation and Management for Newborn, Genetic, Neurologic, and Developmental-Behavioral Disorders (Book 3) 1st Edition 2017

Succinct Pediatrics Evaluation and Management for Newborn, Genetic, Neurologic, and Developmental-Behavioral Disorders (Book 3) 1st Edition 2017

Succinct Pediatrics: Evaluation and Management for Newborn, Genetic, Neurologic, and Developmental-Behavioral Disorders (Book 3) 1st Edition 2017 Succinct Pediatrics: Evaluation and Management for Newborn, Genetic, Neurologic, and Developmental-Behavioral Disorders (Succint Pediatrics) (Book 3) 1st Edition 2017 Obtain evidence-based information to make timely and accurate diagnoses and treatment decisions. Continuing with this volume, Succinct …

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Common Malformations 1st Edition 2011

Common Malformations 1st Edition 2011

Common Malformations 1st Edition 2011 Common Malformations 1st Edition 2011 This extensively illustrated reference work is designed for health professionals who care for newborn infants including neonatologists, pediatricians, NICU nurses, pediatric neurologists, pediatric surgeons, geneticists, and genetic counselors. It describes the most common malformations and draws the information needed for …

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Inborn Metabolic Diseases: Diagnosis and Treatment 6th Edition 2016

Inborn Metabolic Diseases: Diagnosis and Treatment 6th Edition 2016

Inborn Metabolic Diseases: Diagnosis and Treatment 6th Edition 2016 Inborn Metabolic Diseases: Diagnosis and Treatment 6th Edition 2016 This work is recognised as the standard textbook for professionals involved in the diagnosis and management of inborn errors of metabolism (IEM) and an essential resource in this multidisciplinary field. For the …

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The Bedside Dysmorphologist 1st Edition 2007

The Bedside Dysmorphologist 1st Edition 2007

The Bedside Dysmorphologist 1st Edition 2007 The Bedside Dysmorphologist 1st Edition 2007 A highly illustrated field guide to dysmorphology, a key area of clinical genetics and a vital competency for all clinicians. Oxford Genetics is a comprehensive, cross-searchable collection of resources offering quick and easy access to Oxford University Press’s prestigious …

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Signs and Symptoms of Genetic Conditions: A Handbook 1st Edition 2014

Signs and Symptoms of Genetic Conditions: A Handbook 1st Edition 2014

Signs and Symptoms of Genetic Conditions: A Handbook 1st Edition 2014 Signs and Symptoms of Genetic Conditions: A Handbook 1st Edition 2014 Connecting an abnormal physical exam to a possible genetic condition is a daunting and inexact task for any physician, be they a primary care provider, non-geneticist specialist, or …

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