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Genetic Issues in Neonatal Care

Creator:   Catherine Witt
Created:   11/3/2011
Contains:  23 items
Articles published in ANC dealing with genetic and embryologic issues in neonates

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Congenital Central Hypoventilation Syndrome: A Case Report

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Familial Hemophagocytic Lymphohistiocytosis in the Neonate

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Neonatal Experiences of Newborns With Full Trisomy 18

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A Case Study on Walker—Warburg Syndrome

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Recognition and Management of the Infant With Beckwith–Wiedemann Syndrome

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Hemophagocytic Lymphohistiocytosis in the Premature Neonate

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Klippel—Trenaunay Syndrome: A Case Study

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Recognition of Caudal Regression Syndrome

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DOWN SYNDROME

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A Parent's Guide to the Genetics of Down Syndrome

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Assessment and Care of the Newborn With Down Syndrome

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Focus on the Physical Assessment of the Infant With Stickler Syndrome

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Examination of the Newborn With Congenital Scoliosis: Focus on the Physical

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Transient Myeloproliferative Disorder in a Newborn With Down Syndrome

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Congenital Diaphragmatic Hernia: Advanced Physiology and Care Concepts

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Osteogenesis Imperfecta in the Neonate

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Infantile Myofibroma: A Case Report and Review of the Literature

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Epidermolysis Bullosa: A Case Study in Transport, Treatment, and Care

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Prune Belly Syndrome: A Focused Physical Assessment

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PART 2. PHYSICAL ASSESSMENT OF THE INFANT WITH CLEFT LIP AND/OR PALATE

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