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Source: Wikipedia (Herausgeber):

Genodermatoses Turner syndrome, Prader-Willi syndrome, Joubert syndrome, Neurofibromatosis, Von Hippel-Lindau disease, Tuberous sclerosis, Freeman-Sheldon syndrome, Progeria, Treacher-Collins syndrome, Ataxia telangiectasia, Angelman syndrome - new book

2011, ISBN: 1156711746

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Source: Wikipedia (Herausgeber):

Genodermatoses Turner syndrome, Prader-Willi syndrome, Joubert syndrome, Neurofibromatosis, Von Hippel-Lindau disease, Tuberous sclerosis, Freeman-Sheldon syndrome, Progeria, Treacher-Collins syndrome, Ataxia telangiectasia, Angelman syndrome - new book

2011, ISBN: 1156711746

Kartoniert / Broschiert MEDICAL / Dermatology, mit Schutzumschlag 11, [PU:Books LLC, Reference Series]

Shipping costs:Versandkosten innerhalb der BRD. (EUR 2.50) MARZIES.de Buch- und Medienhandel, 14621 Schönwalde-Glien
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Genodermatoses (Paperback) - Paperback

ISBN: 1156711746

[EAN: 9781156711743], Neubuch, Paperback. Chapters: Turner syndrome, Joubert syndrome, Neurofibromatosis, Von Hippel-Lindau disease, Tuberous sclerosis, Freeman-Sheldon syndrome, Progeria… More...

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Genodermatoses Turner Syndrome, Prader-Willi Syndrome, Joubert Syndrome, Neurofibromatosis, Von Hippel-Lindau Disea - Paperback

2011, ISBN: 9781156711743

General Books LLC , Jun-2011. softcover. New. pp. 1198, General Books LLC

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Genodermatoses - new book

2011, ISBN: 9781156711743

PB, Neubuch, pp. 1198., [PU: General Books LLC]

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Bibliographic data of the best matching book

Details of the book
Genodermatoses: Turner syndrome, Prader-Willi syndrome, Joubert syndrome, Neurofibromatosis, Von Hippel-Lindau disease, Tuberous sclerosis, ... Ataxia telangiectasia, Angelman syndrome

Source: Wikipedia. Pages: 116. Chapters: Turner syndrome, Prader-Willi syndrome, Joubert syndrome, Neurofibromatosis, Von Hippel-Lindau disease, Tuberous sclerosis, Freeman-Sheldon syndrome, Progeria, Treacher-Collins syndrome, Ataxia telangiectasia, Angelman syndrome, Johanson-Blizzard syndrome, Dyskeratosis congenita, Heterochromia iridum, Ectrodactyly-ectodermal dysplasia-cleft syndrome, LEOPARD syndrome, X-linked ichthyosis, Epidermolysis bullosa, Noonan syndrome, Bloom syndrome, POEMS syndrome, MELAS syndrome, Proteus syndrome, Keratosis pilaris, Epidermolytic hyperkeratosis, Crouzon syndrome, Keratolytic winter erythema, Costello syndrome, Adams-Oliver syndrome, Lamellar ichthyosis, Xeroderma pigmentosum, Apert syndrome, Klippel-Feil syndrome, Harlequin-type ichthyosis, Ichthyosis bullosa of Siemens, Kabuki syndrome, Werner syndrome, Silver-Russell syndrome, Albright's hereditary osteodystrophy, Infantile Refsum disease, Ichthyosis vulgaris, Oculodentodigital dysplasia, Hypohidrotic ectodermal dysplasia, McCune-Albright syndrome, Cockayne syndrome, Schindler disease, XXYY syndrome, Multiple sulfatase deficiency, Darier's disease, Epidermolysis bullosa dystrophica, Wolf-Hirschhorn syndrome, Acrodermatitis enteropathica, Rothmund-Thomson syndrome, Gardner's syndrome, Hay-Wells syndrome, Netherton syndrome, Papillon-Lefèvre syndrome, Popliteal pterygium syndrome, Cronkhite-Canada syndrome, Hailey-Hailey disease, Cartilage-hair hypoplasia, Pachyonychia congenita, Conradi-Hünermann syndrome, Cardiofaciocutaneous syndrome, Ichthyosis hystrix, Blue rubber bleb nevus syndrome, Kindler syndrome, Zunich-Kaye syndrome, CHILD syndrome, Cutis verticis gyrata, Congenital ichthyosiform erythroderma, Townes-Brocks syndrome, Zimmermann-Laband syndrome, Acrocephalosyndactylia, Pfeiffer syndrome, Van der Woude syndrome, Rombo syndrome, IBIDS syndrome, Clouston's hidrotic ectodermal dysplasia, Marinesco-Sjögren syndrome, Confluent and reticulated papillomatosis of Gougerot and Carteaud, Disseminated superficial actinic porokeratosis, Sjögren-Larsson syndrome, Bazex-Dupré-Christol syndrome, Naegeli-Franceschetti-Jadassohn syndrome, Dermatopathia pigmentosa reticularis, Erythrokeratodermia variabilis, Meleda disease, Holocarboxylase synthetase deficiency, Lhermitte-Duclos disease, Scleroatrophic syndrome of Huriez, Primary hypertrophic osteoathropathy, Ichthyosis follicularis with alopecia and photophobia syndrome, Bart syndrome, Plaque-type porokeratosis, Epidermolysis bullosa simplex, Lelis syndrome, Naxos syndrome, Focal palmoplantar keratoderma with oral mucosal hyperkeratosis, Franceschetti-Klein syndrome, Peeling skin syndrome, Carvajal syndrome, Linear and whorled nevoid hypermelanosis, Atrophodermia vermiculata, Rhizomelic chondrodysplasia punctata, DeSanctis-Cacchione syndrome, Keratosis linearis with ichthyosis congenital and sclerosing keratoderma syndrome, Restrictive dermopathy, Acrokeratosis verruciformis, Recessive dystrophic epidermolysis bullosa, Keratitis-ichthyosis-deafness syndrome, Ectodermal dysplasia with corkscrew hairs, Focal dermal hypoplasia, Dyschromatosis universalis hereditaria, Neutral lipid storage disease, Keratosis pilaris atrophicans faciei, Pachyonychia congenita type I, Jaffe-Campanacci syndrome, Atrichia with papular lesions, Laryngoonychocutaneous syndrome, Incontinentia pigmenti achromians, Hypotrichosis-lymphedema-telangiectasia syndrome, Tricho-rhino-phalangeal syndrome, Polyostotic fibrous dysplasia, Junctiona...

Details of the book - Genodermatoses: Turner syndrome, Prader-Willi syndrome, Joubert syndrome, Neurofibromatosis, Von Hippel-Lindau disease, Tuberous sclerosis, ... Ataxia telangiectasia, Angelman syndrome


EAN (ISBN-13): 9781156711743
ISBN (ISBN-10): 1156711746
Paperback
Publishing year: 2010
Publisher: LIFE JOURNEY
1198 Pages
Weight: 1,565 kg
Language: eng/Englisch

Book in our database since 2010-07-19T19:02:12+01:00 (London)
Detail page last modified on 2022-04-28T12:39:11+01:00 (London)
ISBN/EAN: 9781156711743

ISBN - alternate spelling:
1-156-71174-6, 978-1-156-71174-3
Alternate spelling and related search-keywords:
Book title: lindau, prader willi syndrom, neurofibromatosis, sheldon, joubert, freeman, angelman, von hippel


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