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  • Lingua: Inglese

    Editore: -, 2010

    0521184320 / 9780521184328

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    Paperback. Condizione: Very Good. Velo-Cardio-Facial Syndrome: A Model for Understanding Microdeletion Disorders This book is in very good condition and will be shipped within 24 hours of ordering. The cover may have some limited signs of wear but the pages are clean, intact and the spine remains undamaged. This book has clearly been well maintained and looked after thus far. Money back guarantee if you are not satisfied. See all our books here, order more than 1 book and get discounted shipping.

  • Lingua: Inglese

    Editore: Cambridge University Press 13/01/2011, 2011

    0521184320 / 9780521184328

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    Paperback. Condizione: Very Good. Shipped within 24 hours from our UK warehouse. Clean, undamaged book with no damage to pages and minimal wear to the cover. Spine still tight, in very good condition. Remember if you are not happy, you are covered by our 100% money back guarantee.

  • Lingua: Inglese

    Editore: Cambridge University Press., 2005

    0521821851 / 9780521821858

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    Da: Universitätsbuchhandlung Herta Hold GmbH, Berlin, GermaniaUniversitätsbuchhandlung Herta Hold GmbH

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    1st ed. 18 x 25 cm. 256 pages. Hardcover. Versand aus Deutschland / We dispatch from Germany via Air Mail. Einband bestoßen, daher Mängelexemplar gestempelt, sonst sehr guter Zustand. Imperfect copy due to slightly bumped cover, apart from this in very good condition. Stamped. Sprache: Englisch.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    PAP. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2005

    0521821851 / 9780521821858

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    Da: Labyrinth Books, Princeton, NJ, U.S.A.Labyrinth Books

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    Condizione: Usato - Molto buono

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    Condizione: Very Good.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Condizione: As New. Unread book in perfect condition.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    PAP. Condizione: New. New Book. Shipped from UK. Established seller since 2000.

  • Lingua: Inglese

    Editore: Cambridge University Press, GB, 2010

    0521184320 / 9780521184328

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    EUR 60,24

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    Paperback. Condizione: New. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders.

  • Lingua: Inglese

    Editore: Cambridge University Press, Cambridge, 2010

    0521184320 / 9780521184328

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    Paperback. Condizione: new. Paperback. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by deletion of part of chromosome 22. The focus is clinical issues with chapters devoted to psychiatric disorders, neuroimaging, speech and language, cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. This 2005 book has been authored by leading international VCFS clinicians and researchers. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.

  • Lingua: Inglese

    Editore: Cambridge University Press, GB, 2010

    0521184320 / 9780521184328

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    EUR 63,75

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    Paperback. Condizione: New. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    EUR 58,33

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    Condizione: New. pp. 258 67:B&W 6.69 x 9.61 in or 244 x 170 mm (Pinched Crown) Perfect Bound on White w/Gloss Lam.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Condizione: New. In English.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2011

    0521184320 / 9780521184328

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    Condizione: New. A definitive 2005 text describing the diagnosis, treatment and molecular biology of Velo-cardio-facial Syndrome. Editor(s): Murphy, Kieran C.; Scambler, Peter J. Num Pages: 258 pages, black & white illustrations. BIC Classification: MFN; MJW; MMH. Category: (P) Professional & Vocational. Dimension: 244 x 170 x 14. Weight in Grams: 420. . 2011. Reissue. paperback. . . . .

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Condizione: New.

  • Lingua: Inglese

    Editore: Cambridge University Press 2011-01-13, 2011

    0521184320 / 9780521184328

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    Paperback. Condizione: New.

  • Lingua: Inglese

    Editore: Cambridge Univ Pr, 2011

    0521184320 / 9780521184328

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    Paperback. Condizione: Brand New. reissue edition. 243 pages. 9.50x6.50x0.55 inches. In Stock.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Condizione: As New. Unread book in perfect condition.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Condizione: New. A definitive 2005 text describing the diagnosis, treatment and molecular biology of Velo-cardio-facial Syndrome. Editor(s): Murphy, Kieran C.; Scambler, Peter J. Num Pages: 258 pages, black & white illustrations. BIC Classification: MFN; MJW; MMH. Category: (P) Professional & Vocational. Dimension: 244 x 170 x 14. Weight in Grams: 420. . 2011. Reissue. paperback. . . . . Books ship from the US and Ireland.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Paperback / softback. Condizione: New. New copy - Usually dispatched within 3 working days.

  • Lingua: Inglese

    Editore: Cambridge University Press CUP, 2010

    0521184320 / 9780521184328

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    Condizione: New. pp. 258.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

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    Condizione: New. pp. 258.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

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  • Lingua: Inglese

    Editore: Cambridge University Press, GB, 2010

    0521184320 / 9780521184328

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    Paperback. Condizione: New. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders.

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    EUR 57,22

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    Condizione: New. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by deletion of part of chromosome 22. The focus is clinical issues with chapters devoted to psychiatric disorders, neuroimaging, speech and language, cardiac, ENT, gastrointestinal, ophthalmic .

  • Lingua: Inglese

    Editore: Cambridge University Press, 2010

    0521184320 / 9780521184328

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    Da: AHA-BUCH GmbH, Einbeck, GermaniaAHA-BUCH GmbH

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    EUR 80,27

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    Taschenbuch. Condizione: Neu. Druck auf Anfrage Neuware - Printed after ordering - Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders.

  • Lingua: Inglese

    Editore: Cambridge University Press, Cambridge, 2010

    0521184320 / 9780521184328

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    EUR 95,07

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    Paperback. Condizione: new. Paperback. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by deletion of part of chromosome 22. The focus is clinical issues with chapters devoted to psychiatric disorders, neuroimaging, speech and language, cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. This 2005 book has been authored by leading international VCFS clinicians and researchers. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.

  • Lingua: Inglese

    Editore: Cambridge University Press, GB, 2010

    0521184320 / 9780521184328

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    Paperback. Condizione: New. Velo-Cardio-Facial Syndrome (VCFS) is a genetic disorder caused by the deletion of part of chromosome 22. It occurs in approximately one in 4000 births and there are now more than 100 physical phenotypic features reported. VCFS affects every major system in the body and this 2005 book was the first to describe its full clinical impact. It has been authored by leading international VCFS clinicians/researchers. The focus is on clinical issues with chapters devoted to psychiatric disorders (with the sufferer showing very high levels of schizophrenia), neuroimaging, speech and language disorders, as well as cardiac, ENT, gastrointestinal, ophthalmic and urological manifestations. Molecular genetics, immunodeficiency and genetic counselling are also covered, and practical approaches to diagnosis and treatment described. As VCFS is seen as a paradigm for other microdeletion disorders, this book will not just appeal to clinicians seeing VCFS patients, but also to those interested in other genetic disorders.