9780721606156

Book Description: Saunders. Hardcover. Book Condition: New. 0721606156 New US Hardcover, will ship with free insurance and emailed tracking and confirmation. Bookseller Inventory # NPR-S-DEC11-9780721606156

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Book Description: Elsevier Health Sciences(Elsevier), 2005. Hardback. Book Condition: New. 10.24 by 7.24 inches. (976 pages) The completely revised and updated New Edition of this definitive text-now in full color Long known as the source to consult for guidance on diagnosis, prognosis, plan management, and genetic counseling, this easy-to-use reference focuses on the patterns of human defects caused by inborn errors in morphogenesis as opposed to defects caused by mechanical problems. It provides a wealth of information on normal and abnormal morphogenesis * minor anomalies and their relevance * clinical approaches to specific diagnoses * and normal standards of measurement for the entire spectrum of disorders. Each chapter includes a description of the specific abnormality-including occasional associated abnormalities-natural history, etiology, and references. On opposing pages are several descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality. 1.Recognizable Patterns of Malformation A.Chromosomal Abnormality Syndromes Down Syndrome Trisomy 18 Syndrome Trisomy 13 Syndrome Trisomy 8 Syndrome Trisomy 9 Mosaic Syndrome Triploidy Syndrome and Diploid/Triploid Mixoploidy Syndrome Deletion 3p Syndrome Duplication 3q Syndrome Deletion 4p Syndrome Deletion 4q Syndrome Deletion 5p Syndrome Deletion 9p Syndrome Duplication 10q Syndrome Aniridia-Wilms Tumor Association Deletion 11q Syndrome Deletion 13q Syndrome Duplication 15q Syndrome Deletion 18p Syndrome Deletion 18q Syndrome Cat-Eye Syndrome XYY Syndrome XXY Syndrome, Klinefelter Syndrome XXXY and XXXXY Syndromes XXX and XXXX Syndromes XXXXX Syndrome 45X Syndrome B.Very Small Stature, Not Skeletal Dysplasia Brachmann-De Lange Syndrome Rubinstein-Taybi Syndrome Russell-Silver Syndrome Short Syndrome 3-M Syndrome Mulibrey Nanism Syndrome Dubowitz Syndrome Bloom Syndrome Johanson-Blizzard Syndrome Seckel Syndrome Hallermann-Streiff Syndrome C.Moderate Short Stature, Facial, +/- Genital Smith-Lemli-Opitz Syndrome Kabuki Syndrome Williams Syndrome Noonan Syndrome Costello Syndrome Cardio-Facio-Cutaneous (CFC) Syndrome Aarskog Syndrome Robinow Syndrome Opitz G/BBB Syndrome Floating-Harbor Syndrome D.Senile-Like Appearance Progeria Syndrome Wiedemann-Rautenstrauch Syndrome Werner Syndrome Cockayne Syndrome Rothmund-Thomson Syndrome E.Early Overgrowth with Associated Defects Fragile X Syndrome Sotos Syndrome Weaver Syndrome Marshall-Smith Syndrome Beckwith-Wiedemann Syndrome Simpson-Golabi-Behmel Syndrome F.Unusual Brain and/or Neuromuscular Findings With Associated Defects Amyoplasia Congenita Disruptive Sequence Distal Arthrogryposis Syndrome, Type 1 Pena-Shokeir Phenotype Cerebro-Oculo-Facio-Skeletal (COFS) Syndrome Lethal Multiple Pterygium Syndrome Neu-Laxova Syndrome Restrictive Dermopathy Meckel-Gruber Syndrome Pallister-Hall Syndrome X-Linked Hydrocephalus Spectrum Hydrolethalus Syndrome Walker-Warburg Syndrome Miller-Dieker Syndrome Smith-Magenis Syndrome Ataxia-Telangiectasia Syndrome Menkes Syndrome 22q13 Deletion Syndrome Angelman Syndrome Prader-Willi Syndrome Cohen Syndrome Killian/Teschler-Nicola Syndrome 1p36 Deletion Syndrome Fryns Syndrome Zellweger Syndrome Freeman-Sheldon Syndrome Myotonic Dystrophy Syndrome Schwartz-Jampel Syndrome Marden-Walker Syndrome Schinzel-Giedion Syndrome Acrocallosal Syndrome 3C Syndrome Hecht Syndrome G.Facial Defects As Major Feature Moebius Sequence Blepharophimosis-Ptosis-Epicanthus Inversus Synrome Robin Sequence Cleft Lip Sequence Van Der Woude Syndrome Frontonasal Dysplasia Sequence Fraser Syndrome Melnick-Fraser Syndrome Branchio-Oculo-Facial Syndrome Charge Syndrome Waardenburg Syndrome, Types I and II Treacher Collins Syndrome Marshall Syndrome Cervico-Oculo-Acoustic Syndrome H.Facial-Limb Defects as Major Feature Miller Syndrome Nager Syndrome Townes-Brocks Syndrome Oral-Facial-Digital Syndrome Mohr Syndrome Deletion 22q11.2 Oculodentodigital Syndrome Lenz Microphthalmia Syndrome Oto-Palato-Digital Syndrome, Type I Oto-Palato-Digital Syndrome, Type II Coffin-Lowry Syndrom. Bookseller Inventory # AE0721606156

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Book Description: 2005. Hardback. Book Condition: New. New book. Shipped from UK. Bookseller Inventory # FD-9780721606156

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Book Description: Pending Action, 2005. Hardback. Book Condition: New. New book. Shipped from UK. Bookseller Inventory # BB-9780721606156

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Book Description: Book Condition: New. Bookseller Inventory # 3426340-n

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Book Description: Elsevier Publishers. Book Condition: New. New, This item can not be shipped Internationl. Bookseller Inventory # 0721606156

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Book Description: Pending Action, 2005. Hardback. Book Condition: New. New book. Shipped from UK. Bookseller Inventory # BB-9780721606156

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Book Description: Elsevier Health Sciences, United Kingdom, 2005. Mixed media product. Book Condition: New. 6th Revised edition. 260 x 184 mm. Brand New Book with Free Worldwide Delivery. The completely revised and updated new edition of this definitive text - now in full color! Long known as the source to consult for guidance on diagnosis, prognosis, plan management, and genetic counseling, this easy-to-use reference focuses on the patterns of human defects caused by inborn errors in morphogenesis as opposed to defects caused by mechanical problems. It provides: a wealth of information on normal and abnormal morphogenesis; minor anomalies and their relevance; clinical approaches to specific diagnoses; and, normal standards of measurement for the entire spectrum of disorders. Each chapter includes a description of the specific abnormality - including occasional associated abnormalities - natural history, etiology, and references. On opposing pages are several descriptive photographs and line drawings of either an individual with the abnormality or specific features of the abnormality. Bookseller Inventory # AA59780721606156

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Book Description: Saunders, 2005. Hardcover. Book Condition: New. New copy, in stock and despatched from the UK. In stock and despatched from the UK. UK Orders over 2 kilos in weight will be upgraded to First Class or courier delivery. Bookseller Inventory # 47950

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Book Description: W B Saunders Co, 2005. Hardback. Book Condition: New. New book. Shipped from US. Bookseller Inventory # IB-9780721606156

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