{"product_id":"cassidy-and-allansons-management-of-genetic-syndromes-hardback-9781119432678","title":"Cassidy and Allanson's Management of Genetic Syndromes (Hardback) 9781119432678","description":"\u003cfont face=\"Georgia\"\u003e\r\n\u003cp\u003e\u003cfont size=\"6\"\u003eCassidy and Allanson's Management of Genetic Syndromes\u003c\/font\u003e\u003cbr\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003c\/p\u003e\n\u003cp\u003e\u003cfont size=\"4\"\u003eJohn C. Carey (Edited by), SB Carey (Author), Suzanne B. Cassidy (Edited by), Agatino Battaglia (Edited by), David Viskochil (Edited by)\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e9781119432678, Wiley\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eHardback, published 17 December 2020\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e1104 pages\u003cbr\u003e27.9 x 22.6 x 4.6 cm, 2.903 kg\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\r\n\r\n\r\n\u003cp align=\"justify\"\u003e\u003cstrong\u003e\u003cfont size=\"3\"\u003eDie 4. Auflage dieses Praktikerbuchs ist hochaktuell, bleibt aber ihren Ursprüngen treu. Zu jedem der 59 Krankheitsbilder gibt es aktuelle Informationen zu Identifikation (auch mit neuen Diagnosekriterien), genetischen Grundlagen, Diagnosetests und Management.\u003c\/font\u003e\u003c\/strong\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003e\u003cp\u003eForeword to the Fourth Edition xi\u003c\/p\u003e \u003cp\u003eForeword to the Third Edition xiii\u003c\/p\u003e \u003cp\u003eForeword to the Second Edition xv\u003c\/p\u003e \u003cp\u003eForeword to the First Edition xvii\u003c\/p\u003e \u003cp\u003ePreface xix\u003c\/p\u003e \u003cp\u003eList of Contributors xxi\u003c\/p\u003e \u003cp\u003eIntroduction xxvii\u003c\/p\u003e \u003cp\u003e1 Aarskog Syndrome 1\u003cbr\u003e\u003ci\u003eRoger E. Stevenson\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e2 Achondroplasia 9\u003cbr\u003e\u003ci\u003eRichard M. Pauli and Lorenzo Botto\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e3 Alagille Syndrome 31\u003cbr\u003e\u003ci\u003eHenry C. Lin and Ian D. Krantz\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e4 Albinism: Ocular and Oculocutaneous Albinism and Hermansky–Pudlak Syndrome 45\u003cbr\u003e\u003ci\u003eC. Gail Summers and David R. Adams\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e5 Angelman Syndrome 61\u003cbr\u003e\u003ci\u003eCharles A. Williams and Jennifer M. Mueller-Mathews\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e6 Arthrogryposis 75\u003cbr\u003e\u003ci\u003eJudith G. Hall\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e7 ATR-X: α Thalassemia\/Mental Retardation-X-Linked 93\u003cbr\u003e\u003ci\u003eRichard J. Gibbons\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e8 Bardet–Biedl Syndrome 107\u003cbr\u003e\u003ci\u003eAnne M. Slavotinek\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e9 Beckwith–Wiedemann Syndrome and Hemihyperplasia 125\u003cbr\u003e\u003ci\u003eCheryl Shuman and Rosanna Weksberg\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e10 Cardio-Facio-Cutaneous Syndrome 147\u003cbr\u003e\u003ci\u003eMaria Inês Kavamura and Giovanni Neri\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e11 CHARGE Syndrome 157\u003cbr\u003e\u003ci\u003eDonna M. Martin, Christine A. Oley, and Conny M. van Ravenswaaij-Arts\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e12 Coffin–Lowry Syndrome 171\u003cbr\u003e\u003ci\u003eR. Curtis Rogers\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e13 Coffin–Siris Syndrome 185\u003cbr\u003e\u003ci\u003eTomoki Kosho and Noriko Miyake\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e14 Cohen Syndrome 195\u003cbr\u003e\u003ci\u003eKate E. Chandler\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e15 Cornelia de Lange Syndrome 207\u003cbr\u003e\u003ci\u003eAntonie D. Kline and Matthew Deardorff\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e16 Costello Syndrome 225\u003cbr\u003e\u003ci\u003eBronwyn Kerr, Karen W. Gripp, and Emma M.M. Burkitt Wright\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e17 Craniosynostosis Syndromes 241\u003cbr\u003e\u003ci\u003eElizabeth J. Bhoj and Elaine H. Zackai\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e18 Deletion 1p36 Syndrome 253\u003cbr\u003e\u003ci\u003eAgatino Battaglia\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e19 Deletion 4p: Wolf–Hirschhorn Syndrome 265\u003cbr\u003e\u003ci\u003eAgatino Battaglia\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e20 Deletion 5p Syndrome 281\u003cbr\u003e\u003ci\u003eAntonie D. Kline, Joanne M. Nguyen, and Dennis J. Campbell\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e21 Deletion 22q11.2 (Velo-Cardio-Facial Syndrome\/DiGeorge Syndrome) 291\u003cbr\u003e\u003ci\u003eDonna M. McDonald-McGinn, Stephanie Jeong, Michael-John McGinn II, Elaine H. Zackai, and Marta Unolt\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e22 Deletion 22q13 Syndrome: Phelan–McDermid Syndrome 317\u003cbr\u003e\u003ci\u003eKaty Phelan, R. Curtis Rogers, and Luigi Boccuto\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e23 Denys–Drash Syndrome, Frasier Syndrome, and WAGR Syndrome (\u003ci\u003eWT1\u003c\/i\u003e-related Disorders) 335\u003cbr\u003e\u003ci\u003eJoyce T. Turner and Jeffrey S. Dome\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e24 Down Syndrome 355\u003cbr\u003e\u003ci\u003eAditi Korlimarla, Sarah J. Hart, Gail A. Spiridigliozzi, and Priya S. Kishnani\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e25 Ehlers–Danlos Syndromes 389\u003cbr\u003e\u003ci\u003eBrad T. Tinkle\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e26 Fetal Alcohol Spectrum Disorders 405\u003cbr\u003e\u003ci\u003eH. Eugene Hoyme and Prachi E. Shah\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e27 Fetal Anticonvulsant Syndrome 425\u003cbr\u003e\u003ci\u003eElizabeth A. Conover, Omar Abdul-Rahman, and H. Eugene Hoyme\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e28 Fragile X Syndrome and Premutation-Associated Disorders 443\u003cbr\u003e\u003ci\u003eRandi J. Hagerman\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e29 Gorlin Syndrome: Nevoid Basal Cell Carcinoma Syndrome 459\u003cbr\u003e\u003ci\u003ePeter A. Farndon and D. Gareth Evans\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e30 Hereditary Hemorrhagic Telangiectasia 475\u003cbr\u003e\u003ci\u003eJonathan N. Berg and Anette D. Kjeldsen\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e31 Holoprosencephaly 487\u003cbr\u003e\u003ci\u003ePaul Kruszka, Andrea L. Gropman, and Maximilian Muenke\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e32 Incontinentia Pigmenti 505\u003cbr\u003e\u003ci\u003eDian Donnai and Elizabeth A. Jones\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e33 Inverted Duplicated Chromosome 15 Syndrome (Isodicentric 15) 515\u003cbr\u003e\u003ci\u003eAgatino Battaglia\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e34 Kabuki Syndrome 529\u003cbr\u003e\u003ci\u003eSarah Dugan\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e35 47,XXY (Klinefelter Syndrome) and Related X and Y Chromosomal Conditions 539\u003cbr\u003e\u003ci\u003eCarole Samango-Sprouse, John M. Graham Jr, Debra R. Counts, and Jeannie Visootsak\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e36 Loeys–Dietz Syndrome 563\u003cbr\u003e\u003ci\u003eAline Verstraeten, Harry C. Dietz, and Bart L. Loeys\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e37 Marfan Syndrome 577\u003cbr\u003e\u003ci\u003eUta Francke\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e38 Mowat–Wilson Syndrome 597\u003cbr\u003e\u003ci\u003eDavid Mowat and Meredith Wilson\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e39 Myotonic Dystrophy Type 1 611\u003cbr\u003e\u003ci\u003eIsis B.T. Joosten, Kees Okkersen, Baziel G.M. van Engelen, and Catharina G. Faber\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e40 Neurofibromatosis Type 1 629\u003cbr\u003e\u003ci\u003eDavid Viskochil\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e41 Noonan Syndrome 651\u003cbr\u003e\u003ci\u003eJudith E. Allanson and Amy E. Roberts\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e42 Oculo-Auriculo-Vertebral Spectrum 671\u003cbr\u003e\u003ci\u003eKoenraad Devriendt, Luc De Smet, and Ingele Casteels\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e43 Osteogenesis Imperfecta 683\u003cbr\u003e\u003ci\u003eAn N. Dang Do and Joan C. Marini\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e44 Pallister–Hall Syndrome and Greig Cephalopolysyndactyly Syndrome 707\u003cbr\u003e\u003ci\u003eLeslie G. Biesecker\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e45 Pallister–Killian Syndrome 717\u003cbr\u003e\u003ci\u003eEmanuela Salzano, Sarah E. Raible, and Ian D. Krantz\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e46 Prader–Willi Syndrome 735\u003cbr\u003e\u003ci\u003eShawn E. McCandless and Suzanne B. Cassidy\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e47 Proteus Syndrome 763\u003cbr\u003e\u003ci\u003eLeslie G. Biesecker\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e48 \u003ci\u003ePTEN \u003c\/i\u003eHamartoma Tumor Syndrome 775\u003cbr\u003e\u003ci\u003eJoanne Ngeow and Charis Eng\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e49 Rett Syndrome 791\u003cbr\u003e\u003ci\u003eEric E. Smeets\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e50 Robin Sequence 807\u003cbr\u003e\u003ci\u003eHoward M. Saal\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e51 Rubinstein–Taybi Syndrome 823\u003cbr\u003e\u003ci\u003eLeonie A. Menke and Raoul C. M. Hennekam\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e52 Silver–Russell Syndrome 837\u003cbr\u003e\u003ci\u003eEmma L. Wakeling\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e53 Smith–Lemli–Opitz Syndrome 851\u003cbr\u003e\u003ci\u003eAlicia Latham and Christopher Cunniff\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e54 Smith–Magenis Syndrome 863\u003cbr\u003e\u003ci\u003eAnn C.M. Smith and Andrea L. Gropman\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e55 Sotos Syndrome 895\u003cbr\u003e\u003ci\u003eTrevor R.P. Cole and Alison C. Foster\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e56 Stickler Syndrome 915\u003cbr\u003e\u003ci\u003eMary B. Sheppard and Clair A. Francomano\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e57 Treacher Collins Syndrome and Related Disorders 927\u003cbr\u003e\u003ci\u003eMarilyn C. Jones\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e58 Trisomy 18 and Trisomy 13 Syndromes 937\u003cbr\u003e\u003ci\u003eJohn C. Carey\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e59 Tuberous Sclerosis Complex 957\u003cbr\u003e\u003ci\u003eLaura S. Farach, Kit Sing Au, and Hope Northrup\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e60 Turner Syndrome 977\u003cbr\u003e\u003ci\u003eAngela E. Lin and Melissa L. Crenshaw\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e61 VATER\/VACTERL Association 995\u003cbr\u003e\u003ci\u003eBenjamin D. Solomon and Bryan D. Hall\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e62 Von Hippel–Lindau Syndrome 1005\u003cbr\u003e\u003ci\u003eSamantha E. Greenberg, Luke D. Maese, and Benjamin L. Maughan\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003e63 Williams Syndrome 1021\u003cbr\u003e\u003ci\u003eColleen A. Morris and Carolyn B. Mervis\u003c\/i\u003e\u003c\/p\u003e \u003cp\u003eIndex 1039\u003c\/p\u003e\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\u003cp\u003e\u003cfont size=\"3\"\u003eSubject Areas: Biology, life sciences [\u003ca title=\"See our other books on Biology, life sciences\" href=\"https:\/\/freshlyprintedbooks.co.uk\/search?q=%22Biology,%20life%20sciences%20%5BPS%5D%22\"\u003ePS\u003c\/a\u003e]\u003c\/font\u003e\u003c\/p\u003e\r\n\r\n\r\n\u003c\/font\u003e","brand":"Wiley-Blackwell","offers":[{"title":"Brand New","offer_id":52428585107736,"sku":"9781119432678","price":140.69,"currency_code":"GBP","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0730\/2037\/5320\/files\/9781119432678.jpg?v=1784680518","url":"https:\/\/freshlyprintedbooks.co.uk\/products\/cassidy-and-allansons-management-of-genetic-syndromes-hardback-9781119432678","provider":"Freshly Printed Books","version":"1.0","type":"link"}