Ultrasound of Congenital Fetal Anomalies : Differential Diagnosis and Prognostic Indicators, Second Edition
Dario (Gaslini Children’s Hospital, Genoa, Italy) Paladini
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Statistical Methods in Genetic Epidemiology
Duncan C. (Professor of Preventive Medicine, Director of the B Thomas
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Cancer Cytogenetics : Chromosomal and Molecular Genetic Aberrations of Tumor Cells
Sverre (The Norwegian Radium Hospital, Norway) Heim
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Huntington's Disease
Gillian (, Professor of Neurogenetics, Division of Medical and Bates
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Prader-Willi Syndrome : Development and Manifestations
Joyce (University of Cambridge) Whittington
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Perfusion for Congenital Heart Surgery : Notes on Cardiopulmonary Bypass for a Complex Patient Population
Gregory S. Matte
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Colour Atlas of Paediatric Facial Diagnosis
Trevor P Mann
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Inherited Disorders of the Kidney : Investigation and Management
Steven H. (Consultant Renal Physician, Consultant Renal Physic Morgan
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The Spondylarthritides
Andrei (Consultant Rheumatologist, Consultant Rheumatologist, R Calin
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The Muscular Dystrophies
Alan E H (, Department of Neurology, Royal Devon and Exeter Hos Emery
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Lysosomal Disorders of the Brain : Recent Advances in Molecular and Cellular Pathogenesis and Treatment
Frances (, Glycobiology Institute, Department of Biochemistry, Platt
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Integrating Evolutionary Biology into Medical Education : for maternal and child healthcare students, clinicians, and scientists
Jay (Research Professor, Research Professor, Georgtown Unive Schulkin
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Human Malformations and Related Anomalies
Roger E. (Senior Clinical Geneticist, Senior Clinical Genet Stevenson
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Pediatric and Adult Nutrition in Chronic Diseases, Developmental Disabilities, and Hereditary Metabolic Disorders : Prevention, Assessment, and Treatment
Shirley W. (Adjunct Professor, Adjunct Professor, Nova Univers Ekvall
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Duchenne Muscular Dystrophy
Alan E. H. (Emeritus Professor of Human Genetics, University of Emery
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Hereditary Hearing Loss and Its Syndromes
Helga V. (Director of Clinical Genetics, Director of Clinica Toriello
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Management of Prader-Willi Syndrome
Merlin Butler
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Genetics Diagnosis, Inborn Errors of Metabolism and Newborn Screening: An Update, An Issue of Clinics in Perinatology : Volume 42-2
Michael J. (Emory University, Atlanta, GA) Gambello
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The Tricuspid Valve in Congenital Heart Disease
Alessandro Giamberti
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Living with Genetic Disorder : The Impact of Neurofibromatosis 1
Joan Ablon
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Fragile X Syndrome : Diagnosis, Treatment, and Research
Randi Jenssen (Professor) Hagerman
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The Encyclopedia of Genetic Disorders and Birth Defects
James Wynbrandt
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Sickle Cell and the Social Sciences : Health, Racism and Disablement
Simon (De Montfort University, UK) Dyson
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Muscular Dystrophy Therapeutics : Methods and Protocols
Rika Maruyama
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