| 000 -LEADER |
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06600nam a22005535i 4500 |
| 001 - CONTROL NUMBER |
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| control field |
978-3-540-30361-9 |
| 003 - CONTROL NUMBER IDENTIFIER |
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| control field |
DE-He213 |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
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| control field |
20161121230601.0 |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION |
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cr nn 008mamaa |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
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| fixed length control field |
100301s2005 gw | s |||| 0|eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| International Standard Book Number |
9783540303619 |
| -- |
978-3-540-30361-9 |
| 024 7# - OTHER STANDARD IDENTIFIER |
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| Standard number or code |
10.1007/3-540-30361-8 |
| Source of number or code |
doi |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER |
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| Classification number |
R895-920 |
| 072 #7 - SUBJECT CATEGORY CODE |
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| Subject category code |
MMPH |
| Source |
bicssc |
| 072 #7 - SUBJECT CATEGORY CODE |
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| Subject category code |
MMP |
| Source |
bicssc |
| 072 #7 - SUBJECT CATEGORY CODE |
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| Subject category code |
MED008000 |
| Source |
bisacsh |
| 082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER |
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| Classification number |
616.0757 |
| Edition number |
23 |
| 100 1# - MAIN ENTRY--PERSONAL NAME |
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| Personal name |
Castriota-Scanderbeg, Alessandro. |
| Relator term |
author. |
| 245 10 - TITLE STATEMENT |
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| Title |
Abnormal Skeletal Phenotypes |
| Medium |
[electronic resource] : |
| Remainder of title |
From Simple Signs to Complex Diagnoses / |
| Statement of responsibility, etc. |
by Alessandro Castriota-Scanderbeg, Bruno Dallapiccola. |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
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| Place of production, publication, distribution, manufacture |
Berlin, Heidelberg : |
| Name of producer, publisher, distributor, manufacturer |
Springer Berlin Heidelberg, |
| Date of production, publication, distribution, manufacture, or copyright notice |
2005. |
| 300 ## - PHYSICAL DESCRIPTION |
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| Extent |
XIV, 962 p. |
| Other physical details |
online resource. |
| 336 ## - CONTENT TYPE |
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| Content type term |
text |
| Content type code |
txt |
| Source |
rdacontent |
| 337 ## - MEDIA TYPE |
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| Media type term |
computer |
| Media type code |
c |
| Source |
rdamedia |
| 338 ## - CARRIER TYPE |
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| Carrier type term |
online resource |
| Carrier type code |
cr |
| Source |
rdacarrier |
| 347 ## - DIGITAL FILE CHARACTERISTICS |
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| File type |
text file |
| Encoding format |
PDF |
| Source |
rda |
| 505 0# - FORMATTED CONTENTS NOTE |
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| Formatted contents note |
I -- Skull -- Thorax -- Spine -- Pelvis -- Long Bones -- Hands -- Feet -- Joints -- Generalized Skeletal Abnormalities -- II -- Aarskog Syndrome -- Achondrogenesis, Type IB -- Achondrogenesis, Type II -- Achondroplasia -- Acrofacial Dysostosis, Nager Type -- Angelman Syndrome -- Apert Syndrome -- Asphyxiating Thoracic Dysplasia -- Atelosteogenesis -- Bardet-Biedl Syndrome -- Beckwith-Wiedemann Syndrome -- C Syndrome -- Campomelic Dysplasia -- Carpenter Syndrome -- Cerebro-costo-mandibular Syndrome -- CHARGE Association -- Chondrodysplasia Punctata, Conradi-Hünermann Type -- Chondrodysplasia Punctata, Rhizomelic Type -- Chondrodysplasia Punctata, Brachytelephalangic Type -- Chondroectodermal Dysplasia -- Chromosome 4p- Syndrome -- Chromosome Trisomy 13 Syndrome -- Chromosome Trisomy 18 Syndrome -- Chromosome Trisomy 21 Syndrome -- Cleidocranial Dysplasia -- Cockayne Syndrome -- Coffin-Lowry Syndrome -- Coffin-Siris Syndrome -- Cohen Syndrome -- Craniometaphyseal Dysplasia, Dominant Type -- Cri-du-chat Syndrome -- Crouzon Syndrome -- De Lange Syndrome -- Diaphyseal Dysplasia -- Diastrophic Dysplasia -- Dubowitz Syndrome -- Dyschondrosteosis -- Dysosteosclerosis -- Ectodermal Dysplasias -- Ehlers-Danlos Syndromes -- Enchondromatosis -- Exostoses, Multiple -- Fanconi Anemia -- Focal Dermal Hypoplasia Syndrome -- Freeman-Sheldon Syndrome -- Frontometaphyseal Dysplasia -- Goldenhar Syndrome -- Hallermann-Streiff Syndrome -- Holt-Oram Syndrome -- Kenny-Caffey Syndrome -- Klippel-Feil Anomaly -- Klippel-Trenaunay-Weber Syndrome -- Kniest Dysplasia -- Larsen Syndrome -- Marfan Syndrome -- McCune-Albright Syndrome -- Meckel Syndrome -- Melnick-Needles Syndrome -- Melorheostosis -- Mental Retardation, X-Linked, Associated with FRA Xq27.3 -- Mesomelic Dwarfism, Langer Type -- Mesomelic Dwarfism, Nievergelt Type -- Metatropic Dysplasia -- Multiple Epiphyseal Dysplasia -- Nail-Patella Syndrome -- Nevoid Basal Cell Carcinoma Syndrome -- Noonan Syndrome -- Opitz Syndrome -- Oro-facio-digital Syndrome, Type I -- Oro-facio-digital Syndrome, Type II -- Osteogenesis Imperfecta, Type I -- Osteogenesis Imperfecta, Type IIA -- Osteogenesis Imperfecta, Type IIB/III -- Osteopathia Striata with Cranial Sclerosis -- Osteopetrosis, Infantile Type -- Osteopetrosis, Adult Type -- Osteopoikilosis -- Oto-palato-digital Syndrome, Type I -- Oto-palato-digital Syndrome, Type II -- Pena-Shokeir Syndrome -- Pfeiffer Syndrome -- Poland Syndrome -- Prader-Willi Syndrome -- Progeria -- Pseudoachondroplasia -- Pyknodysostosis -- Roberts Syndrome -- Robin Sequence -- Robinow Syndrome -- Rubinstein-Taybi Syndrome -- Saethre-Chotzen Syndrome -- Seckel Syndrome -- Short Rib-Polydactyly Syndrome, Type I -- Short Rib-Polydactyly Syndrome, Type II -- Silver-Russell Syndrome -- Smith-Lemli-Opitz Syndrome -- Sotos Syndrome -- Spondyloepimetaphyseal Dysplasia, Irapa Type -- Spondyloepimetaphyseal Dysplasia, Strudwick Type -- Spondyloepiphyseal Dysplasia Congenita -- Spondyloepiphyseal Dysplasia Tarda -- Spondylometaphyseal Dysplasia, Kozlowski Type -- Stickler Syndrome -- Thanatophoric Dysplasia -- Thrombocytopenia-Absent Radius Syndrome -- Treacher-Collins Syndrome -- Tricho-rhino-phalangeal Syndrome, Type I -- Tricho-rhino-phalangeal Syndrome, Type II -- Turner Syndrome -- VATER Association -- Williams Syndrome. |
| 520 ## - SUMMARY, ETC. |
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| Summary, etc. |
When one is asked to review a manuscript in order of the different parts of the skeleton and comprises to write a foreword,one always asks oneself,“Is there about 600 pages. anything special about this book?”“Does it supply The reader will ?nd something about the in- us with unique information?”I hesitate to think how dence, anatomic location, pathogenesis, differential many years ago it was when I ?rst discussed with diagnosis, diagnostic relevance, and, if known, Dr. Alessandro Castriota-Scanderbeg the possible the pattern of inheritance.This approach to the s- publication of this book. It may well have been a ject, which is essentially symptom-based, contrasts decade ago. I seem to remember that I encouraged markedly with the conventional texts that either s- him to write a text that was truly different from the tematically report a given disorder or list the features classic ones. that form a gamut. That this most remarkable ?rst edition is unique is In addition, the authors provide a second part of easily illustrated. I have personally picked an area I 300 pages in which they cover approximately 100 am less familiar with. In Chap. 2,“The Thorax,”the syndromes, congenital anomaly syndromes, skeletal following sections are covered: embryology of the dysplasias, and chromosomal disorders to aid in thorax, abnormal shape and size of the chest, small major differential diagnosis. Of special value is the thorax and various conditions that exhibit that sign. presentation of variability of the condition with age. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Medicine. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Human genetics. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Human anatomy. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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Radiology. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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Internal medicine. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Orthopedics. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Pediatrics. |
| 650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Medicine & Public Health. |
| 650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Imaging / Radiology. |
| 650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Internal Medicine. |
| 650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Anatomy. |
| 650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Human Genetics. |
| 650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Pediatrics. |
| 650 24 - SUBJECT ADDED ENTRY--TOPICAL TERM |
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| Topical term or geographic name entry element |
Orthopedics. |
| 700 1# - ADDED ENTRY--PERSONAL NAME |
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| Personal name |
Dallapiccola, Bruno. |
| Relator term |
author. |
| 710 2# - ADDED ENTRY--CORPORATE NAME |
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| Corporate name or jurisdiction name as entry element |
SpringerLink (Online service) |
| 773 0# - HOST ITEM ENTRY |
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| Title |
Springer eBooks |
| 776 08 - ADDITIONAL PHYSICAL FORM ENTRY |
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| Relationship information |
Printed edition: |
| International Standard Book Number |
9783540679974 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS |
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| Uniform Resource Identifier |
http://dx.doi.org/10.1007/3-540-30361-8 |
| 912 ## - |
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ZDB-2-SME |
