Detalles del Título
Detalles del Título

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Título Atlas of Mental Retardation SyndromesLibros / Impreso - Libros
Autor(es) Gellis, Sydney S. (Autor)
Feingold, Murray (Autor)
Rutman, Joel Y. (Autor)
Publicación Washington D. C : U.S. Departmen of Health, Education, and Welfare, 1968
Descripción Física 188p
Idioma Inglés;
Clasificación(es) 157.8
Materia(s) Deficiencia mental; RETRASADOS MENTALES;
Resumen Con: Achondroplasia, p. 3 Albright's Hereditary Osteodystrophy, p. 5 Apert's Syndrome, p. 7 Ataxia-Telangiectasia, p. 9 Bird-Headed Dwarf, p. 11 Bloom's Syndrome, p. 13 Cebocephaly, p. 15 Cerebral Gigantism, p. 17 Cerebro-Hepato-Renal Syndrome, p. 19 Chondrodystrophia Calcificans Congenita, p. 21 Chromosome 18, Partial Deleetion of the Long Arm, p. 23 Cri du Chat, p. 25 Crouzon's Disease, p. 27 Cyclopia, p. 29 Cytomegalic Inclusion Disease, Congenital, p. 31 De Lange's Syndrome, p. 33 Diencephalic Syndrome, p. 35 Down's Syndrome, p. 37 Ectodermal Dysplasia, p. 39 Ellis-Van Creveld Syndrome, p. 41 Familial Dysautonomia, p. 43 Ganliosidosis, Generalized, p. 45 Hallerman-Streiff Syndrome, p. 47 Happy Puppet Syndrome, p. 49 Hydranencephaly, p. 51 Hydrocephalus, Congenital, p. 53 Hypercalcemia, Infantile, p. 55 Hypertelorism, Ocular, p. 57 Hyperuricemia, p. 59 Hypoclycemia (nenonatal): Macroglossia, p. 61 Hypothyroidism, Congenital, p. 63 Kernicterus, p. 65 Kleeblattschadel, Syndrome, p. 67 Klinefelter's Syndrome, p. 69 Laurence-Moon-Biedl Syndrome, p. 71 Leprechaunism, 83 Lipogranulomatosis, p. 75 Marinesco-Sjögren Syndrome, p. 77 Median Cleft Face Syndrome, p. 79 Metaphyseal Dysplasia, Familial, p. 81 Microcephaly, Familial, p. 83 Mucopolysaccharidosis-Hunter's, p. 85 Mucopolysaccharidosis-Hurler's, p. 87 Mucopolysaccharidosis-Morquio's, p. 89 Mucopolysaccharidosis-Sanfilippo, p. 91 Mucopolysaccharidosis-Scheie, p. 93 Myotonic Dystrophy, p. 95 Neurodegenerative Disease With Monilethrix, p. 97 Neurofibromatosis, p. 99 Nevoid-Basal Cell Carcinoma Syndrome, p. 101 Niemann-Pick Disease.p. 103 Oculo-Auriculo-Vertebral Dysplasia, p. 105 Oculo-Cerebro-Renal Syndrome, p. 107 Oculo-Dental-Digital Dysplasia, p. 109 Oral-Facial-Digital Syndrome, p. 111 Osteogeneis imperfecta, p.113 Osteopetrosis, p. 115 Oto-Palato-Digital, p. 117 Phenylketonuria, p. 119 Pierre Robin Syndrome, p. 121 Popliteal Pterygia Syndrome, p. 123 Prader-Willi Syndrome, p. 125 Progeria, p. 127 Pygnodysostosis, p. 129 Riegeer's Syndrome, p. 131 Ring Chromosome 18, p. 133 Rubella, Congenital, p. 135 rubinstein's Syndrome, p. 137 Sebaceous Nevi Linear, Convulsions, and Mental Retardation, p. 139 Silver's Syndrome, p. 141 Sjögren-Larsson Syndrome, p. 143 Smith-Lemli-Opitz Syndrome, p. 145 Sturge-Weber Disease, p. 147 Syphilis, Congenital, p. 149 Toxoplasmosis, Congenital, p. 151 Treacher Collins Syndrome, p. 153 Trisomy 13-15, p. 155 Trysomy 17-18, p. 157 Tuberous Sclerosis, p. 159 Turner's Syndrome, p. 161 Turner's Syndrome, Male, p. 163 Waardenburg Syndrome, p. 165 Wilson's Disease, p. 167 Index of Clinical Characteristics, p. 168 I 187
Disponibilidad
CodBarras Localización Ubicación Habitual Signatura Estado Categoría Solicitar
0000009438Universidad de San Buenaventura - Sede BogotáColección Depósito 157.8 / G319aIDisponibleGeneralSolicitar