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Oral manifestations of inherited disorders /

Oral Manifestations of Inherited Disorders.

Detalles Bibliográficos
Clasificación:Libro Electrónico
Autores principales: Sedano, Heddie O., Sauk, John J. (Autor), Gorlin, Robert J., 1923-2006 (Autor)
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Boston : Butterworths, �1977.
Temas:
Acceso en línea:Texto completo

MARC

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060 4 |a WU 290  |b S447o 1977 
082 0 4 |a 616/.042 
084 |a XG 2479  |2 rvk 
084 |a YP 4519  |2 rvk 
100 1 |a Sedano, Heddie O. 
245 1 0 |a Oral manifestations of inherited disorders /  |c Heddie O. Sedano, John J. Sauk, Jr., Robert J. Gorlin. 
260 |a Boston :  |b Butterworths,  |c �1977. 
300 |a 1 online resource (viii, 214 pages) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
504 |a Includes bibliographical references and index. 
506 |3 Use copy  |f Restrictions unspecified  |2 star  |5 MiAaHDL 
533 |a Electronic reproduction.  |b [Place of publication not identified] :  |c HathiTrust Digital Library,  |d 2010.  |5 MiAaHDL 
538 |a Master and use copy. Digital master created according to Benchmark for Faithful Digital Reproductions of Monographs and Serials, Version 1. Digital Library Federation, December 2002.  |u http://purl.oclc.org/DLF/benchrepro0212  |5 MiAaHDL 
583 1 |a digitized  |c 2010  |h HathiTrust Digital Library  |l committed to preserve  |2 pda  |5 MiAaHDL 
588 0 |a Print version record. 
505 0 |a Cover image; Title page; Table of Contents; Copyright; Preface; Chapter 1: Genetic Counseling and Oral Examination; Publisher Summary; 1.1 Genetic Counseling; 1.2 Physical Examination of the Oral Cavity; 1.3 Radiologic Interpretation of Some Oral and Paraoral Structures; Chapter 2: Some Inherited Conditions Affecting Only Calcified Dental Tissue; Publisher Summary; 2.1 Amelogenesis Imperfecta; 2.2 Coronal Dentin Dysplasia; 2.3 Hereditary Opalescent Dentin; 2.4 Radicular Dentin Dysplasia; Chapter 3: Systemic Inherited Disorders with Dental Involvement; Publisher Summary; 3.1 Acroosteolysis 
505 8 |a 3.2 Amelocerebrohypohidrosis Syndrome3.3 Cryptodontic Brachymetacarpalia; 3.4 Hypodontia and Nail Dysgenesis; 3.5 Hypophosphatasia (Phosphoethanolaminuria); 3.6 Hypophosphatemic Vitamin D-Resistant Rickets; 3.7 Hypoplastic-Hypocalcified Enamel, Onycholysis, and Functional Hypohidrosis; 3.8 Incontinentia Pigmenti; 3.9 Oculodentoosseous Dysplasia; 3.10 Otodental Syndrome; 3.11 Pseudohypoparathyroidism and Pseudopseudohypoparathyroidism; 3.12 Rothmund-Thomson Syndrome; Chapter 4: Systemic Inherited Disorders with Oral or Perioral Soft Tissue Involvement; Publisher Summary 
505 8 |a 4.1 Acrodermatitis Enteropathica4.2 Bloom Syndrome; 4.3 Ch�ediak-Higashi Syndrome; 4.4 Congenital Indifference to Pain; 4.5 Cutis Laxa; 4.6 Cyclic Neutropenia; 4.7 Double Lip, Blepharochalasis, and Nontoxic Thyroid Enlargement; 4.8 Dyskeratosis Congenita with Pigmentation, Dystrophic Nails, Aplastic Anemia, and Leukoplakia Oris; 4.9 Fabry Syndrome; 4.10 Familial Dysautonomia; 4.11 Gingival Fibromatosis with Ear, Nose, Bone, and Nail Defects and Hepatosplenomegaly; 4.12 Gingival Fibromatosis with Hypertrichosis, Epilepsy, and Mental Retardation 
505 8 |a 4.13 Gingival Fibromatosis with Multiple Hyaline Fibromas4.14 Hereditary Benign Intraepithelial Dyskeratosis; 4.15 Hereditary Hemorrhagic Telangiectasia; 4.16 Hermansky-Pudlak Syndrome; 4.17 Hyperkeratosis Palmoplantaris and Attached Gingival Hyperkeratosis; 4.18 Lesch-Nyhan Syndrome; 4.19 Moebius Syndrome; 4.20 Multiple Hamartoma and Neoplasia Syndrome; 4.21 Multiple Mucosal Neuromas, Medullary Carcinoma of the Thyroid, Pheochromocytoma, and Marfanoid Body Build with Muscle Wasting; 4.22 Neurofibromatosis; 4.23 Pachydermoperiostosis; 4.24 Pachyonychia Congenita, Jadassohn-Lewandowski Type 
505 8 |a 4.25 Peutz-Jeghers Syndrome4.26 Pseudoxanthoma Elasticum; 4.27 Xerodermic Idiocy; 4.28 White Sponge Nevus; Chapter 5: Systemic Inherited Disorders with Involvement of Jaw Bones; Publisher Summary; 5.1 Apert Syndrome; 5.2 Carpenter Syndrome; 5.3 Cerebrohepatorenal Syndrome; 5.4 Cherubism; 5.5 Chondrodysplasia Punctata; 5.6 Craniofacial Dysostosis; 5.7 Craniometaphyseal Dysplasia and Craniodiaphyseal Dysplasia; 5.8 Infantile Cortical Hyperostosis; 5.9 Mandibulofacial Dysostosis; 5.10 Marfan Syndrome; 5.11 Melnick-Needles Syndrome; 5.12 Mucopolysaccharidosis VII; 5.13 Pfeiffer Syndrome 
520 |a Oral Manifestations of Inherited Disorders. 
650 0 |a Oral manifestations of general diseases. 
650 0 |a Medical genetics. 
650 0 |a Genetic disorders. 
650 2 |a Genetic Diseases, Inborn  |0 (DNLM)D030342 
650 2 |a Oral Manifestations  |0 (DNLM)D009912 
650 2 |a Genetics, Medical  |0 (DNLM)D005826 
650 6 |a Manifestations buccales des maladies.  |0 (CaQQLa)201-0012237 
650 6 |a G�en�etique m�edicale.  |0 (CaQQLa)201-0001432 
650 6 |a Maladies g�en�etiques.  |0 (CaQQLa)201-0024547 
650 7 |a Genetic disorders  |2 fast  |0 (OCoLC)fst00940009 
650 7 |a Medical genetics  |2 fast  |0 (OCoLC)fst01014133 
650 7 |a Oral manifestations of general diseases  |2 fast  |0 (OCoLC)fst01047086 
650 7 |a Erbkrankheit  |2 gnd  |0 (DE-588)4015106-2 
655 7 |a Orale Manifestation.  |2 swd 
700 1 |a Sauk, John J.,  |e author. 
700 1 |a Gorlin, Robert J.,  |d 1923-2006,  |e author. 
776 0 8 |i Print version:  |a Sedano, Heddie O.  |t Oral manifestations of inherited disorders.  |d Boston : Butterworths, �1977  |w (DLC) 77008363  |w (OCoLC)3003104 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780409950502  |z Texto completo