Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis / / by Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk |
Autore | Wyandt Herman Edwin <1939-> |
Edizione | [2nd ed. 2017.] |
Pubbl/distr/stampa | Singapore : , : Springer Singapore : , : Imprint : Springer, , 2017 |
Descrizione fisica | 1 online resource (XX, 490 p. 87 illus., 29 illus. in color.) |
Disciplina | 611.01816 |
Soggetto topico |
Medical genetics
General practice (Medicine) Gene Function General Practice / Family Medicine |
ISBN | 981-10-3035-9 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto | Introduction -- Chromosome Heteromorphism -- Frequencies of Heteromorphisms -- Clinical Populations -- Euchromatic Variants -- Chromosome Heteromorphism (Summaries)- Fragile Sites -- Chromosome Variation Detected by Fluorescent In Situ Hybridization (FISH) -- Array-Comparative Genomic Hybridization/Microarray Analysis: Interpretation of Copy Number variants -- A CNV Catalog -- Gene and Genome Sequencing: Interpreting Genetic Variation at the Nucleotide Level. . |
Record Nr. | UNINA-9910253910803321 |
Wyandt Herman Edwin <1939-> | ||
Singapore : , : Springer Singapore : , : Imprint : Springer, , 2017 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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Pediatric Imaging : Rapid-Fire Questions and Answers / / by: Quattromani, Frank |
Autore | Handal Gilbert A |
Pubbl/distr/stampa | New York, : Thieme, c2008 |
Descrizione fisica | 1 online resource (469 p.) |
Disciplina | 618.92/00754 |
Soggetto topico |
Pediatric diagnostic imaging
Diagnostic imaging |
ISBN |
1-63853-061-0
1-282-89125-1 9786612891250 1-58890-659-0 |
Formato | Materiale a stampa |
Livello bibliografico | Monografia |
Lingua di pubblicazione | eng |
Nota di contenuto |
Pediatric Imaging: Rapid-Fire Questions and Answers; Title Page; Copyright; Dedication; Contents; Preface; Acknowledgments; Contributors; 1 Airway/Head and Neck; Adenoids; Antrochoanal Polyp; Cephalocele; CHARGE Acronym; Choanal Atresia; Chordoma (Clivus; Spheno-occipital); Congenital and Other Head and Neck Masses; Croup; Cystic Hygroma; Epiglottitis (Supraglottitis); Familial Dysautonomia (Riley-Day Syndrome); Foreign Body Aspiration; Glottic and Subglottic Obstruction; Gorlin Syndrome (Basal Cell Carcinoma Syndrome); Head and Neck Masses (see also Congenital Head and Neck Masses)
Hereditary Angioneurotic Edema (HAE Quincke Disease/Quincke Edema); Hurler Syndrome; Juvenile-Onset Recurrent Respiratory Laryngeal Papillomas (JLP); Juvenile Nasopharyngeal Angiofibroma (JNA); Laryngocele; Laryngomalacia; Laryngotracheoesophageal Cleft; Lymphangioma; Macroglossia; Mandible; Membranous Croup (Bacterial Tracheitis); Mucocele; Nasal Polyps; Pierre Robin Sequence (PRS); Retropharyngeal Abscess; Retropharyngeal Soft Tissue Thickening; Sinuses; Stridor; Subglottic Hemangioma; Supraglottic Obstruction; Subglottic Stenosis; Thyroglossal Duct Cyst; Tracheal Stenosis; Tracheomalacia Tumors of the AirwayVascular Rings; Vocal Cord Paralysis; Wegener Disease; 2 Allergy/Immunology/Rheumatology; B-Cell System Antibody or Humoral Immunity; T-Cell Cellular Immunity; Phagocyte Cell Disorder; Complement Disorders; 3 Pediatric Cardiac Imaging; Aberrant Left Pulmonary Artery (LPA) Pulmonary Sling; Acyanotic Congenital Heart Disease (CHD); Anomalous Left Coronary Arising from Pulmonary Artery (ALCAPA); Anomalous Pulmonary Venous Return; Total Anomalous Pulmonary Venous Return (TAPVR); Aortic Aneurysm; Aortic Arch; Aortic Dilatation; Aortic Interruption; Aortic Stenosis Asplenia Syndrome (Ivemark Syndrome)/HeterotaxyAtrial Enlargement; Atrial Septal Defect (ASD); Cantrell Pentalogy; Cardiac Malpositions; Cardiac Tumors (in Childhood); Cerebral Emboli Associated with CHD; Coarctation of the Aorta; Congenital Heart Disease (CHD); Congestive Heart Failure (CHF); Cor Triatriatum; Cyanosis in the Neonate; Cyanotic Congenital Heart Disease; Cyanosis with Decreased Pulmonary Vascularity; Cyanosis with Increased Pulmonary Vascularity; Ventricle Double-Outlet Right (DORV); Ebstein Malformation; Eisenmenger Syndrome; Ellis Van Creveld (EVC) Syndrome Embryology of the HeartEndocardial Cushion Defect (ECD) (Atrioventricular Septal Defect); Glycogen Storage Disease; Holt-Oram Syndrome; Hypertension (HTN); Hypoplastic Left Heart Syndrome (HLHS); Kartagener Syndrome; Kawasaki Disease (Infantile Periateritis Nodosa); Left-to-Right Shunts; Lutembacher Complex; Marfan Syndrome; Noonan Syndrome; Patent Duct Arteriosus (PDA); Polysplenia; Pulmonary Artery Stenosis; Pulmonary Circulation; Pulmonary Venous Pressure; Pulmonic Valve Stenosis; Supravalvular Pulmonary Stenosis (SPS); Infundibular Pulmonary Stenosis (Subvalvular); Scimitar Syndrome Shone Anomaly |
Record Nr. | UNINA-9910781289603321 |
Handal Gilbert A | ||
New York, : Thieme, c2008 | ||
Materiale a stampa | ||
Lo trovi qui: Univ. Federico II | ||
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