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100426s1977 maua ob 001 0 eng d |
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|z 77008363
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|a OCLCE
|b eng
|e pn
|c OCLCE
|d OCLCQ
|d OCLCO
|d UIU
|d OCLCQ
|d IDEBK
|d OCLCF
|d OCLCO
|d E7B
|d YDXCP
|d OCLCQ
|d OCLCO
|d OCLCQ
|d OCLCA
|d LUN
|d OCLCQ
|d UKAHL
|d VLY
|d OCLCO
|d OCL
|d OCLCQ
|d OCLCO
|d INARC
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019 |
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|a 658140947
|a 878132530
|a 901618818
|a 974618123
|a 974665329
|a 1100952964
|a 1409369109
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|z 0409950505
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|z 9780409950502
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|a 9781483192680
|q (e-book)
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020 |
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|a 1483192687
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035 |
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|a (OCoLC)609520446
|z (OCoLC)658140947
|z (OCoLC)878132530
|z (OCoLC)901618818
|z (OCoLC)974618123
|z (OCoLC)974665329
|z (OCoLC)1100952964
|z (OCoLC)1409369109
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042 |
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|a dlr
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050 |
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4 |
|a RC815
|b .S455
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060 |
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4 |
|a WU 290
|b S447o 1977
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082 |
0 |
4 |
|a 616/.042
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|a XG 2479
|2 rvk
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084 |
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|a YP 4519
|2 rvk
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100 |
1 |
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|a Sedano, Heddie O.
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245 |
1 |
0 |
|a Oral manifestations of inherited disorders /
|c Heddie O. Sedano, John J. Sauk, Jr., Robert J. Gorlin.
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260 |
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|a Boston :
|b Butterworths,
|c �1977.
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300 |
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|a 1 online resource (viii, 214 pages) :
|b illustrations
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336 |
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|a text
|b txt
|2 rdacontent
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337 |
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|a computer
|b c
|2 rdamedia
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338 |
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|a online resource
|b cr
|2 rdacarrier
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504 |
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|a Includes bibliographical references and index.
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506 |
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|3 Use copy
|f Restrictions unspecified
|2 star
|5 MiAaHDL
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533 |
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|a Electronic reproduction.
|b [Place of publication not identified] :
|c HathiTrust Digital Library,
|d 2010.
|5 MiAaHDL
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538 |
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|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
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583 |
1 |
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|a digitized
|c 2010
|h HathiTrust Digital Library
|l committed to preserve
|2 pda
|5 MiAaHDL
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588 |
0 |
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|a Print version record.
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505 |
0 |
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|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
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505 |
8 |
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|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
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505 |
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|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
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505 |
8 |
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|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
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505 |
8 |
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|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
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520 |
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|a Oral Manifestations of Inherited Disorders.
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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 |
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|a Sauk, John J.,
|e author.
|
700 |
1 |
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|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
|