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150509s2011 pau o 000 0 eng d |
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|a 923525864
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|a 9781451166842
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|a 1451166842
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|z (OCoLC)923525864
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|a RL793 .G46 2011
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|a 616.5/042
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|a UAMI
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|a Spitz, Joel L.
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|a Genodermatoses :
|b a Clinical Guide to Genetic Skin Disorders.
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| 250 |
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|a 2nd ed.
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| 260 |
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|a Philadelphia :
|b Wolters Kluwer Health,
|c 2011.
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| 300 |
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|a 1 online resource (420 pages)
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| 336 |
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|a text
|b txt
|2 rdacontent
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|a computer
|b c
|2 rdamedia
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|a online resource
|b cr
|2 rdacarrier
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|a Print version record.
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|a Genodermatoses:A Clinical Guide to Genetic Skin Disorders; Foreword; Preface; Acknowledgments; Contributors; Introduction; Contents; Disorders of Cornification; Ichthyosis Vulgaris; X-linked Ichthyosis; Epidermolytic Hyperkeratosis; Lamellar Ichthyosis; Congenital Ichthyosiform Erythroderma (CIE); Harlequin Fetus; Sjögren-Larsson Syndrome; Refsum Syndrome; Conradi-Hünermann Syndrome; CHILD Syndrome; Netherton Syndrome; Erythrokeratoderma Variabilis; KID Syndrome; Diffuse Palmoplantar Keratoderma (PPK); Howel-Evans Syndrome; Vohwinkel Syndrome; Mal de Meleda; Papillon-Lefèvre Syndrome.
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| 505 |
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|a Richner-Hanhart SyndromeDarier Disease; Epidermal Nevus Syndrome; Suggested Reading; Chapter 2; Disorders of Pigmentation; Oculocutaneous Albinism Type 1 (OCA1); Oculocutaneous Albinism Type II (OCA2); Hermansky-Pudlak Syndrome; Chédiak-Higashi Syndrome; Griscelli Syndrome; Piebaldism; Waardenburg Syndrome; Hypomelanosis of Ito; Incontinentia Pigmenti; LEOPARD Syndrome; Carney Complex; McCune-Albright Syndrome; Neurofibromatosis I; Neurofibromatosis II; Tuberous Sclerosis; Suggested Reading; Disorders of Vascularization; Sturge-Weber Syndrome; Klippel-Trenaunay Syndrome; Cobb Syndrome.
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| 505 |
8 |
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|a Proteus SyndromeBeckwith-Wiedemann Syndrome; Von Hippel-Lindau Syndrome; Ataxia-Telangiectasia; Hereditary Hemorrhagic TelangiectasiaSyndrome; Cutis Marmorata Telangiectatica Congenita; Maffucci Syndrome; Blue Rubber Bleb Nevus Syndrome; Kasabach-Merritt Syndrome; Diffuse Neonatal Hemangiomatosis; PHACE Syndrome; Suggested Reading; Disorders of Connective Tissue; Ehlers-Danlos Syndrome; Marfan Syndrome; Cutis Laxa; Pseudoxanthoma Elasticum; Osteogenesis Imperfecta; Buschke-Ollendorff Syndrome; Focal Dermal Hypoplasia; Lipoid Proteinosis; Progeria; Werner Syndrome; Aplasia Cutis Congenita.
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| 505 |
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|a Suggested ReadingDisorders With Malignant Potential; Basal Cell Nevus Syndrome; Xeroderma Pigmentosum; Muir-Torre Syndrome; Dyskeratosis Congenita; Gardner Syndrome; Peutz-Jeghers Syndrome; Cowden Syndrome; Multiple Endocrine Neoplasia Type IIb; Birt-Hogg-Dube Syndrome; Suggested Reading; EpidermolysisBullosa; Epidermolysis Bullosa Simplex; Junctional Epidermolysis Bullosa (JEB); Dystrophic Epidermolysis Bullosa; Suggested Reading; Disorders of PorphyrinMetabolism; Porphyria Cutanea Tarda (PCT); Variegate Porphyria (VP); Acute Intermittent Porphyria (AIP); Hereditary Coproporphyria (HCP).
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| 505 |
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|a Erythropoietic Protoporphyria (EPP)Congenital Erythropoietic Porphyria (CEP); Hepatoerythropoietic Porphyria (HEP); Suggested Reading; Disorders WithPhotosensitivity; Bloom Syndrome; Rothmund-Thomson Syndrome; Cockayne Syndrome; Trichothiodystrophy; Hartnup Disease; Suggested Reading; Disorders With Immunodeficiency; Wiskott-Aldrich Syndrome; Chronic Granulomatous Disease; Hyper-Immunoglobulin E Syndrome; Severe Combined Immunodeficiency; Hereditary Angioedema; Suggested Reading; Disorders of Hair and Nails; Menkes' Syndrome; Björnstad Syndrome; Argininosuccinic Aciduria; Monilethrix.
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| 500 |
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|a Uncombable Hair Syndrome.
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| 590 |
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|a ProQuest Ebook Central
|b Ebook Central Academic Complete
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| 650 |
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0 |
|a Skin
|x Diseases
|x Genetic aspects.
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| 650 |
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6 |
|a Peau
|x Maladies
|x Aspect génétique.
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| 650 |
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7 |
|a Skin
|x Diseases
|x Genetic aspects
|2 fast
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| 776 |
0 |
8 |
|i Print version:
|a Spitz, Joel L.
|t Genodermatoses : A Clinical Guide to Genetic Skin Disorders.
|d Philadelphia : Wolters Kluwer Health, ©2011
|z 9780781740883
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| 856 |
4 |
0 |
|u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=3418275
|z Texto completo
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| 938 |
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|a ProQuest Ebook Central
|b EBLB
|n EBL2032562
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| 994 |
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|a 92
|b IZTAP
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