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Smith`s Recognizable Patterns Of Human Malformation - David W. Smith
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David W. Smith:

Smith`s Recognizable Patterns Of Human Malformation - used book

ISBN: 9780721606156

ID: INF3003079900

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. Reviews REVIEW OF THE LAST EDITION: `This volume is an invaluable reference for all those engaged in the areas of genetics, dysmorphology, pediatrics, and internal medicine. Dr. Jones should be congratulated for perpetuating this great book....A magnificent contribution to the field.`-Archives of Pediatrics & Adolescent Medicine Features Provides over 1,450 photographs and illustrations to depict each malformation-many from the personal collections of Drs. Smith and Jones-to aid readers in diagnosis.Uses a consistent chapter format to help readers quickly and easily find information on any given disorderOffers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation. What`s NewOffers a clearer understanding of abnormalities through the use of more than 1,000 new full-color figures and photographs.Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome \* Deleletion 22q13 syndrome \* Meier-Gorlin Syndrome \* Short Syndrome \* 3-C Syndrome \* GAPO Syndrome \* Lenz Microphthalmia Syndrome \* Muenke Craniosynostosis \* Torriello-Carey Syndrome \* Mandibulo-Acral Syndrome \* Mowat-Wilson Syndrome \* Ulnar-Mammary Syndrome \* Kaufman-McKusick Syndrome \* Smith-Maginess Syndrome \* Wiedeman-Rautenstrauch Syndrome \* and Shprintzen-Golberg Syndrome.Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts Smith`s Recognizable Patterns Of Human Malformation: 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. Reviews REVIEW OF THE LAST EDITION: `This volume is an invaluable reference for all those engaged in the areas of genetics, dysmorphology, pediatrics, and internal medicine. Dr. Jones should be congratulated for perpetuating this great book....A magnificent contribution to the field.`-Archives of Pediatrics & Adolescent Medicine Features Provides over 1,450 photographs and illustrations to depict each malformation-many from the personal collections of Drs. Smith and Jones-to aid readers in diagnosis.Uses a consistent chapter format to help readers quickly and easily find information on any given disorderOffers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation. What`s NewOffers a clearer understanding of abnormalities through the use of more than 1,000 new full-color figures and photographs.Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome \* Deleletion 22q13 syndrome \* Meier-Gorlin Syndrome \* Short Syndrome \* 3-C Syndrome \* GAPO Syndrome \* Lenz Microphthalmia Syndrome \* Muenke Craniosynostosis \* Torriello-Carey Syndrome \* Mandibulo-Acral Syndrome \* Mowat-Wilson Syndrome \* Ulnar-Mammary Syndrome \* Kaufman-McKusick Syndrome \* Smith-Maginess Syndrome \* Wiedeman-Rautenstrauch Syndrome \* and Shprintzen-Golberg Syndrome.Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts Missbildungen, Oxford Elsevier Ltd

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Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) - Kenneth Jones
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Kenneth Jones:

Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) - hardcover

2005, ISBN: 0721606156

ID: 14068253600

[EAN: 9780721606156], [PU: Saunders], Medical|Pathophysiology, This Book is in Good Condition. Clean Copy With Light Amount of Wear. 100% Guaranteed. Summary: 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 AniridiaWilms 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 BrachmannDe 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 Syndrome X-Linked ?-Thalassemia/Mental Retardation (ATR-X) Syndrome FG Syndrome Stickler Syndrome Catel-Manzke Syndrome Langer-Giedion Syndrome Tricho-Rhino-Phalangeal Syndrome, Type I EctrodactylyEctodermal Dysplasia

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Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) - Kenneth Jones
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Kenneth Jones:
Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) - hardcover

2005

ISBN: 0721606156

ID: 20051314566

[EAN: 9780721606156], Neubuch, [PU: Saunders], Medical|Pathophysiology, Brand New, Unread Copy in Perfect Condition. A+ Customer Service! Summary: 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 AniridiaWilms 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 BrachmannDe 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 Syndrome X-Linked ?-Thalassemia/Mental Retardation (ATR-X) Syndrome FG Syndrome Stickler Syndrome Catel-Manzke Syndrome Langer-Giedion Syndrome Tricho-Rhino-Phalangeal Syndrome, Type I EctrodactylyEctodermal Dysplasia

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Smith's Recognizable Patterns Of Human Malformation - Smith, David W.
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Smith, David W.:
Smith's Recognizable Patterns Of Human Malformation

EAN: 9780721606156

ID: 9780721606156

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. Reviews REVIEW OF THE LAST EDITION:´This volume is an invaluable reference for all those engaged in the areas of genetics, dysmorphology, pediatrics, and internal medicine. Dr. Jones should be congratulated for perpetuating this great book....A magnificent contribution to the field.´-Archives of Pediatrics & Adolescent Medicine Features Provides over 1,450 photographs and illustrations to depict each malformation-many from the personal collections of Drs. Smith and Jones-to aid readers in diagnosis.Uses a consistent chapter format to help readers quickly and easily find information on any given disorderOffers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation.What's NewOffers a clearer understanding of abnormalities through the use of more than 1,000 new full-color figures and photographs.Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome * Deleletion 22q13 syndrome * Meier-Gorlin Syndrome * Short Syndrome * 3-C Syndrome * GAPO Syndrome * Lenz Microphthalmia Syndrome * Muenke Craniosynostosis * Torriello-Carey Syndrome * Mandibulo-Acral Syndrome * Mowat-Wilson Syndrome * Ulnar-Mammary Syndrome * Kaufman-McKusick Syndrome * Smith-Maginess Syndrome * Wiedeman-Rautenstrauch Syndrome * and Shprintzen-Golberg Syndrome.Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts</P></BODY> varia, /200, [PU: Saunders Publishing]

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Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) - Kenneth Jones
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Kenneth Jones:
Smith's Recognizable Patterns Of Human Malformation Sixth Edition (Smith's Recognizable Patterns of Human Malformation) - used book

ISBN: 0721606156

ID: 2552484

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.Provides over 1,450 photographs and illustrations to depict each malformation-many from the personal collections of Drs. Smith and Jones-to aid readers in diagnosis.Uses a consistent chapter format to help readers quickly and easily find information on any given disorderOffers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation.Offers a clearer understanding of abnormalities through the use of more than 1,000 new full-color basic sciences,clinical,diseases,diseases and physical ailments,health fitness and dieting,internal medicine,medical books,medicine,medicine and health sciences,pathology Pathology, Saunders

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Details of the book
Smith's Recognizable Patterns Of Human Malformation
Author:

Smith, David W.

Title:

Smith's Recognizable Patterns Of Human Malformation

ISBN:

9780721606156

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. Reviews REVIEW OF THE LAST EDITION: "This volume is an invaluable reference for all those engaged in the areas of genetics, dysmorphology, pediatrics, and internal medicine. Dr. Jones should be congratulated for perpetuating this great book....A magnificent contribution to the field."-Archives of Pediatrics & Adolescent Medicine Features Provides over 1,450 photographs and illustrations to depict each malformation-many from the personal collections of Drs. Smith and Jones-to aid readers in diagnosis.Uses a consistent chapter format to help readers quickly and easily find information on any given disorderOffers the most current coverage available on existing disorders and their molecular basis, plus the very latest information on virtually any genetic or physiological malformation. What's NewOffers a clearer understanding of abnormalities through the use of more than 1,000 new full-color figures and photographs.Includes updates for every disorder, with extensive new information on the molecular basis of malformations as well as new clinical information for many disorders.Covers 16 additional commonly seen disorders, including Deletion 1p36 syndrome * Deleletion 22q13 syndrome * Meier-Gorlin Syndrome * Short Syndrome * 3-C Syndrome * GAPO Syndrome * Lenz Microphthalmia Syndrome * Muenke Craniosynostosis * Torriello-Carey Syndrome * Mandibulo-Acral Syndrome * Mowat-Wilson Syndrome * Ulnar-Mammary Syndrome * Kaufman-McKusick Syndrome * Smith-Maginess Syndrome * Wiedeman-Rautenstrauch Syndrome * and Shprintzen-Golberg Syndrome.Presents a wealth of new Growth Charts, plus complete revisions to existing Growth Charts

Details of the book - Smith's Recognizable Patterns Of Human Malformation


EAN (ISBN-13): 9780721606156
ISBN (ISBN-10): 0721606156
Hardcover
Publishing year: 2005
Publisher: Elsevier LTD, Oxford
954 Pages
Weight: 2,313 kg
Language: eng/Englisch

Book in our database since 30.05.2007 01:52:38
Book found last time on 22.12.2016 13:54:14
ISBN/EAN: 9780721606156

ISBN - alternate spelling:
0-7216-0615-6, 978-0-7216-0615-6

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