MARC details
| 000 -LEADER |
|---|
| fixed length control field |
14573cam a2200469 i 4500 |
| 001 - CONTROL NUMBER |
|---|
| control field |
GVRL3FQF |
| 003 - CONTROL NUMBER IDENTIFIER |
|---|
| control field |
MiFhGG |
| 005 - DATE AND TIME OF LATEST TRANSACTION |
|---|
| control field |
20241102175636.0 |
| 006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS |
|---|
| fixed length control field |
m o d |
| 007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION |
|---|
| fixed length control field |
cr un ---uuuua |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
|---|
| fixed length control field |
100119s2011 miua obe 001 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
|---|
| International Standard Book Number |
9781414476056 |
| Qualifying information |
|
| 035 ## - SYSTEM CONTROL NUMBER |
|---|
| System control number |
(OCoLC)611868396 |
| 040 ## - CATALOGING SOURCE |
|---|
| Original cataloging agency |
MiFhGG |
| Language of cataloging |
eng |
| Transcribing agency |
MiFhGG |
| Description conventions |
rda |
| -- |
pn |
| 050 #4 - LIBRARY OF CONGRESS CALL NUMBER |
|---|
| Classification number |
RB155.5 |
| 060 00 - NATIONAL LIBRARY OF MEDICINE CALL NUMBER |
|---|
| Classification number |
QZ 13 |
| Item number |
G1517 2011 |
| 245 04 - TITLE STATEMENT |
|---|
| Title |
The Gale encyclopedia of genetic disorders / |
| Statement of responsibility, etc. |
Laurie J. Fundukian, editor. |
| 246 13 - VARYING FORM OF TITLE |
|---|
| Title proper/short title |
Encyclopedia of genetic disorders |
| 246 13 - VARYING FORM OF TITLE |
|---|
| Title proper/short title |
Genetic disorders |
| 250 ## - EDITION STATEMENT |
|---|
| Edition statement |
3rd edition. |
| 264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE |
|---|
| Place of production, publication, distribution, manufacture |
Farmington Hills, Mich. : |
| Name of producer, publisher, distributor, manufacturer |
Gale, |
| Date of production, publication, distribution, manufacture, or copyright notice |
[(c)2011.] |
| 300 ## - PHYSICAL DESCRIPTION |
|---|
| Extent |
1 online resource (2 volumes) : |
| Other physical details |
color illustrations |
| 336 ## - CONTENT TYPE |
|---|
| Content type term |
text |
| Content type code |
txt |
| Source |
rdacontent |
| 337 ## - MEDIA TYPE |
|---|
| Media type term |
computer |
| Media type code |
c |
| Source |
rdamedia |
| 338 ## - CARRIER TYPE |
|---|
| Carrier type term |
online resource |
| Carrier type code |
cr |
| Source |
rdacarrier |
| 347 ## - DIGITAL FILE CHARACTERISTICS |
|---|
| File type |
data file |
| Source |
rda |
| 490 0# - SERIES STATEMENT |
|---|
| Series statement |
Gale eBooks |
| 504 ## - BIBLIOGRAPHY, ETC. NOTE |
|---|
| Bibliography, etc. note |
Includes bibliographies and index. |
| 505 0# - FORMATTED CONTENTS NOTE |
|---|
| Formatted contents note |
22q13 deletion syndrome -- |
| Title |
Aarskog syndrome -- |
| -- |
Aase syndrome -- |
| -- |
Abetalipoproteinemia -- |
| -- |
Absence of vas deferens -- |
| -- |
Acardia -- |
| -- |
Accutane embryopathy -- |
| -- |
Aceruloplasminemia -- |
| -- |
Achondrogenesis -- |
| -- |
Achondroplasia -- |
| -- |
ACHOO syndrome -- |
| -- |
Acrocallosal syndrome -- |
| -- |
Acromegaly -- |
| -- |
Adams-Oliver syndrome -- |
| -- |
Adelaide-type craniosynostosis -- |
| -- |
Adenylosuccinate lyase deficiency -- |
| -- |
Adrenoleukodystrophy -- |
| -- |
Aicardi syndrome -- |
| -- |
Ala dehydratase deficiency -- |
| -- |
Alagille syndrome -- |
| -- |
Albinism -- |
| -- |
Alcoholism -- |
| -- |
Alexander disease -- |
| -- |
Alkaptonuria -- |
| -- |
Alpha-1 antitrypsin -- |
| -- |
Alpha-thalassemia X-linked mental retardation syndrome -- |
| -- |
Alstrom syndrome -- |
| -- |
Alzheimer's disease -- |
| -- |
Amelia -- |
| -- |
Amelogenesis imperfecta -- |
| -- |
Amniocentesis -- |
| -- |
Amyoplasia -- |
| -- |
Amyotrophic lateral sclerosis -- |
| -- |
Androgen insensitivity syndrome -- |
| -- |
Anemia, sideroblastic X-linked -- |
| -- |
Anencephaly -- |
| -- |
Angelman syndrome -- |
| -- |
Ankylosing spondylitis -- |
| -- |
Apert syndrome -- |
| -- |
Arginase deficiency -- |
| -- |
Arnold-Chiari malformation -- |
| -- |
Arthrogryposis multiplex congenita -- |
| -- |
Arthropathy-camptodactyly syndrome -- |
| -- |
Asperger syndrome -- |
| -- |
Asplenia -- |
| -- |
Asthma -- |
| -- |
Astrocytoma -- |
| -- |
Attention deficit hyperactivity disorder -- |
| -- |
Autism -- |
| -- |
Azorean disease -- |
| -- |
Bardet-biedl syndrome -- |
| -- |
Barth syndrome -- |
| -- |
Bassen-Kornzweig syndrome -- |
| -- |
Batten disease -- |
| -- |
Beals disease -- |
| -- |
Beare-Stevenson cutis gyrata syndrome -- |
| -- |
Beckwith-Wiedemann syndrome -- |
| -- |
Beta thalassemia -- |
| -- |
Bicuspid aortic valve -- |
| -- |
Biotinidase deficiency -- |
| -- |
Bipolar disorder -- |
| -- |
Birt-Hogg-Dube syndrome -- |
| -- |
Bloom syndrome -- |
| -- |
Blue rubber bleb nevus syndrome -- |
| -- |
Brachydactyly -- |
| -- |
Branchiootorenal syndrome -- |
| -- |
Breast cancer -- |
| -- |
Bruton agammaglobulinemia -- |
| -- |
Burger-Grutz syndrome -- |
| -- |
Campomelic dysplasia -- |
| -- |
Canavan disease -- |
| -- |
Cancer -- |
| -- |
Cancer genetics -- |
| -- |
Cardiofaciocutaneous syndrome -- |
| -- |
Carnitine palmitoyltransferase deficiency -- |
| -- |
Carpenter syndrome -- |
| -- |
Caudal dysplasia -- |
| -- |
Cayler cardiofacial syndrome -- |
| -- |
Celiac disease -- |
| -- |
Central core disease -- |
| -- |
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy -- |
| -- |
Cerebral palsy -- |
| -- |
Channelopathies -- |
| -- |
Charcot-Marie-Tooth disease -- |
| -- |
Charge syndrome -- |
| -- |
Chediak-Higashi syndrome -- |
| -- |
Chondrodysplasia punctata -- |
| -- |
Chondrosarcoma -- |
| -- |
Choroideremia -- |
| -- |
Chromosomal abnormalities -- |
| -- |
Chromosome -- |
| -- |
Chromosome map -- |
| -- |
Cleft lip and palate -- |
| -- |
Cleidocranial dysplasia -- |
| -- |
Clubfoot -- |
| -- |
Cockayne syndrome -- |
| -- |
Coffin-Lowry syndrome -- |
| -- |
Coffin-Siris syndrome -- |
| -- |
Cohen syndrome -- |
| -- |
Collagenopathy, types II and XI -- |
| -- |
Coloboma -- |
| -- |
Color blindness -- |
| -- |
Compression neuropathy -- |
| -- |
Cone-Rod dystrophy -- |
| -- |
Congenital adrenal hyperplasia -- |
| -- |
Congenital heart disease -- |
| -- |
Congenital hypothyroid syndrome -- |
| -- |
Congenital methemoglobinemia -- |
| -- |
Conjoined twins -- |
| -- |
Conotruncal anomaly face syndrome -- |
| -- |
Corneal dystrophy -- |
| -- |
Cornelia de lange syndrome -- |
| -- |
Corpus callosum, agenesis -- |
| -- |
Costello syndrome -- |
| -- |
Cowden syndrome -- |
| -- |
Crane-Heise syndrome -- |
| -- |
Craniosynostosis -- |
| -- |
Cri du chat syndrome -- |
| -- |
Crouzon syndrome -- |
| -- |
Crouzonodermoskeletal syndrome -- |
| -- |
Cystic fibrosis -- |
| -- |
Cystinosis -- |
| -- |
Cystinuria -- |
| -- |
Dandy-walker malformation -- |
| -- |
De Grouchy syndrome -- |
| -- |
Deletion 22q11 syndrome -- |
| -- |
Dementia -- |
| -- |
Dentatorubral-pallidoluysian atrophy -- |
| -- |
Dent's disease -- |
| -- |
Depression -- |
| -- |
Diabetes -- |
| -- |
Diastrophic dysplasia -- |
| -- |
Distal arthrogryposis syndrome -- |
| -- |
DNA (deoxyribonucleic acid) -- |
| -- |
Donohue syndrome -- |
| -- |
Down syndrome -- |
| -- |
Duane retraction syndrome -- |
| -- |
Dubowitz syndrome -- |
| -- |
Duchenne muscular dystrophy -- |
| -- |
Dyschondrosteosis -- |
| -- |
Dysplasia -- |
| -- |
Dystonia -- |
| -- |
Ectodermal dysplasia -- |
| -- |
Ectrodactyly-ectodermal dysplasia-clefting syndrome -- |
| -- |
Ehlers-Danlos syndrome -- |
| -- |
Ellis-van Creveld syndrome -- |
| -- |
Emery-Dreifuss muscular dystrophy -- |
| -- |
Encephalocele -- |
| -- |
Engelmann disease -- |
| -- |
Entrapment neuropathy -- |
| -- |
Epidermolysis bullosa -- |
| -- |
Epilepsy -- |
| -- |
Erythropoietic porphyria -- |
| -- |
Erythropoietic protoporphyria -- |
| -- |
Essential hypertension -- |
| -- |
Essential tremor -- |
| -- |
Fabry disease -- |
| -- |
Facioscapulohumeral muscular dystrophy -- |
| -- |
Factor V Leiden thrombophilia -- |
| -- |
Fahr disease -- |
| -- |
Familial adenomatous polyposis -- |
| -- |
Familial dysautonomia -- |
| -- |
Familial Mediterranean fever -- |
| -- |
Familial nephritis -- |
| -- |
Familial pulmonary arterial hypertension -- |
| -- |
Fanconi anemia -- |
| -- |
Fanconi-Bickel syndrome -- |
| -- |
Fetal alcohol syndrome -- |
| -- |
FG syndrome -- |
| -- |
Fibroblast growth factor receptor mutations -- |
| -- |
Fluorescent in situ hybridization -- |
| -- |
Fragile x syndrome -- |
| -- |
Fraser syndrome -- |
| -- |
Freeman-Sheldon syndrome -- |
| -- |
Friedreich ataxia -- |
| -- |
Frontonasal dysplasia -- |
| -- |
Frontotemporal dementia -- |
| -- |
Fryns syndrome -- |
| -- |
Galacktokinase deficiency -- |
| -- |
Galactosemia -- |
| -- |
Gastric cancer -- |
| -- |
Gastroschisis -- |
| -- |
Gaucher disease -- |
| -- |
Gene -- |
| -- |
Gene mutations -- |
| -- |
Gene pool -- |
| -- |
Gene therapy -- |
| -- |
Genetic counseling -- |
| -- |
Genetic disorders -- |
| -- |
-- Genetic mapping -- |
| -- |
Genetic testing -- |
| -- |
Genetics and congenital anomalies -- |
| -- |
Genitalia, ambiguous -- |
| -- |
Genome -- |
| -- |
Genome sequencing -- |
| -- |
Genotype and phenotype -- |
| -- |
Gerstmann-Straussler-Scheinker disease -- |
| -- |
Glaucoma -- |
| -- |
Glycogen storage diseases -- |
| -- |
Goltz syndrome -- |
| -- |
GM1-gangliosidosis -- |
| -- |
Greig cephalopolysyndactyly -- |
| -- |
Griscelli syndrome -- |
| -- |
Haim-Munk syndrome -- |
| -- |
Hair loss syndromes -- |
| -- |
Hallermann-Streiff syndrome -- |
| -- |
Hand-foot-uterus syndrome -- |
| -- |
Harlequin fetus -- |
| -- |
Hemifacial microsomia -- |
| -- |
Hemihypertrophy (hemihyperplasia) -- |
| -- |
Hemochromatosis -- |
| -- |
Hemolytic-uremic syndrome -- |
| -- |
Hemophilia -- |
| -- |
Hepatocellular carcinoma -- |
| -- |
Herceptin -- |
| -- |
Hereditary angioneurotic edema -- |
| -- |
Hereditary colorectal cancer -- |
| -- |
Hereditary coproporphyria -- |
| -- |
Hereditary desmoid disease -- |
| -- |
Hereditary hearing loss and deafness -- |
| -- |
Hereditary multiple exostoses -- |
| -- |
Hereditary nonpolyposis colorectal cancer -- |
| -- |
Hereditary pancreatitis -- |
| -- |
Hereditary spastic paraplegia -- |
| -- |
Hereditary spherocytosis -- |
| -- |
Hermansky-Pudlak syndrome -- |
| -- |
Hermaphroditism -- |
| -- |
Hirschsprung disease -- |
| -- |
Holoprosencephaly -- |
| -- |
Holt-Oram syndrome -- |
| -- |
Homocystinuria -- |
| -- |
Human genome project -- |
| -- |
Huntington disease -- |
| -- |
Hydrocephalus -- |
| -- |
Hydrolethalus syndrome -- |
| -- |
Hydrops fetalis -- |
| -- |
Hyperlipoproteinemia -- |
| -- |
Hyperoxaluria -- |
| -- |
Hyperphenylalaninemia -- |
| -- |
Hypochondrogenesis -- |
| -- |
Hypochondroplasia -- |
| -- |
Hypophosphatasia -- |
| -- |
Hypophosphatemia -- |
| -- |
Hypospadias and epispadias -- |
| -- |
Ichthyosis -- |
| -- |
Imprinting -- |
| -- |
Incontinentia pigmenti -- |
| -- |
Infantile Refsum disease -- |
| -- |
Inheritance -- |
| -- |
Inherited arrhythmia -- |
| 505 8# - FORMATTED CONTENTS NOTE |
|---|
| Formatted contents note |
Jackson-Weiss syndrome -- |
| Title |
Jacobsen syndrome -- |
| -- |
Jervell and Lange-Nielsen syndrome -- |
| -- |
Joubert syndrome -- |
| -- |
Kabuki syndrome -- |
| -- |
Kallmann syndrome -- |
| -- |
Kartagener syndrome -- |
| -- |
Karyotype -- |
| -- |
Kennedy disease -- |
| -- |
Klinefelter syndrome -- |
| -- |
Klippel-Feil syndrome -- |
| -- |
Klippel-Trenaunay-Weber syndrome -- |
| -- |
Kniest dysplasia -- |
| -- |
Krabbe disease -- |
| -- |
Langer-Saldino achondrogenesis -- |
| -- |
Larsen syndrome -- |
| -- |
Laterality sequence -- |
| -- |
Leber congenital amaurosis -- |
| -- |
Lebers hereditary optic atrophy -- |
| -- |
Leigh syndrome -- |
| -- |
Lesch-Nyhan syndrome -- |
| -- |
Leukodystrophy -- |
| -- |
Li-Fraumeni syndrome -- |
| -- |
Limb-girdle muscular dystrophy -- |
| -- |
Lipoprotein lipase deficiency -- |
| -- |
Lissencephaly -- |
| -- |
Long QT syndrome -- |
| -- |
Lowe oculocerebrorenal syndrome -- |
| -- |
Machado-Joseph disease -- |
| -- |
Macular degeneration, age-related -- |
| -- |
Major histocompatibility complex -- |
| -- |
Malignant hyperthermia -- |
| -- |
Mannosidosis -- |
| -- |
Marfan syndrome -- |
| -- |
Marshall syndrome -- |
| -- |
Marshall-Smith syndrome -- |
| -- |
MCAD deficiency -- |
| -- |
McCune-Albright syndrome -- |
| -- |
McKusick-Kaufman syndrome -- |
| -- |
Meckel-Gruber syndrome -- |
| -- |
Meckel's diverticulum -- |
| -- |
Menkes syndrome -- |
| -- |
Metaphyseal dysplasia -- |
| -- |
Methylmalonic acidemia -- |
| -- |
Methylmalonicaciduria due to methylmalonic CoA mutase deficiency -- |
| -- |
Micro syndrome -- |
| -- |
Microcephaly (childhood) -- |
| -- |
Microphthalmia with linear skin defects (MLS) -- |
| -- |
Miller-Dieker syndrome -- |
| -- |
Moebius syndrome -- |
| -- |
Monosomy 1p36 syndrome -- |
| -- |
Mowat-Wilson syndrome -- |
| -- |
Moyamoya -- |
| -- |
Mucolipidosis -- |
| -- |
Mucopolysaccharidoses -- |
| -- |
Mucopolysaccharidosis type I, Mucopolysaccharidosis type II -- |
| -- |
Muir-Torre syndrome -- |
| -- |
Multifactorial inheritance -- |
| -- |
Multiple endocrine neoplasias -- |
| -- |
Multiple epiphyseal dysplasia -- |
| -- |
Multiple lentigines syndrome -- |
| -- |
Multiple sclerosis -- |
| -- |
Multiplex ligation-dependent probe amplification -- |
| -- |
Muscular dystrophy -- |
| -- |
Myasthenia gravis -- |
| -- |
Myopia -- |
| -- |
Myotonic dystrophy -- |
| -- |
Myotubular myopathy -- |
| -- |
Nail-patella syndrome -- |
| -- |
Nance-Insley syndrome -- |
| -- |
Narcolepsy -- |
| -- |
Nephrogenic diabetes insipidus -- |
| -- |
Neu-Laxova syndrome -- |
| -- |
Neural tube defects -- |
| -- |
Neuraminidase deficiency -- |
| -- |
Neuraminidase deficiency with beta-galactosidase deficiency -- |
| -- |
Neurofibromatosis -- |
| -- |
Nevoid basal cell carcinoma -- |
| -- |
Niemann-Pick disease -- |
| -- |
Nijmegen breakage syndrome -- |
| -- |
Nonketotic hyperglycemia -- |
| -- |
Noonan syndrome -- |
| -- |
Norrie disease -- |
| -- |
Oculo-digito-esophago-duodenal syndrome -- |
| -- |
Oculodentodigital syndrome -- |
| -- |
Oligohydramnios sequence -- |
| -- |
Omphalocele -- |
| -- |
Oncogene -- |
| -- |
Opitz syndrome -- |
| -- |
Oral-facial-digital syndrome -- |
| -- |
Organic acidemias -- |
| -- |
Ornithine transcarbamylase deficiency -- |
| -- |
Osler-Weber-Rendu syndrome -- |
| -- |
Osteoarthritis -- |
| -- |
Osteogenesis imperfecta -- |
| -- |
Osteoporosis -- |
| -- |
Osteosarcoma -- |
| -- |
Otopalatodigital syndrome -- |
| -- |
Ovarian cancer -- |
| -- |
Paine syndrome -- |
| -- |
Pallister-Hall syndrome -- |
| -- |
Pallister Killian syndrome -- |
| -- |
Pancreatic beta cell agenesis -- |
| -- |
Pancreatic cancer -- |
| -- |
Panic disorder -- |
| -- |
Pantothenate kinase-associated neurodegeneration (PKAN) -- |
| -- |
Parkinson disease -- |
| -- |
Paroxysmal nocturnal hemoglobinuria -- |
| -- |
Patent ductus arteriosus -- |
| -- |
Pedigree analysis -- |
| -- |
Pelizaeus-Merzbacher disease -- |
| -- |
Pendred syndrome -- |
| -- |
Pervasive developmental disorders -- |
| -- |
Peutz-Jeghers syndrome -- |
| -- |
Pfeiffer syndrome -- |
| -- |
Pharmacogenetics -- |
| -- |
Phenylketonuria -- |
| -- |
Pierre-Robin sequence -- |
| -- |
Pituitary dwarfism -- |
| -- |
Poland anomaly -- |
| -- |
Polycystic kidney disease -- |
| -- |
Polycystic ovary syndrome -- |
| -- |
Polydactyly -- |
| -- |
Pompe disease -- |
| -- |
Porphyrias -- |
| -- |
Prader-Willi syndrome -- |
| -- |
Prenatal ultrasound -- |
| -- |
Prion diseases -- |
| -- |
Progeria syndrome -- |
| -- |
Propionic acidemia -- |
| -- |
Prostate cancer -- |
| -- |
Protein C deficiency -- |
| -- |
Protein S deficiency -- |
| -- |
Proteus syndrome -- |
| -- |
Prune-Belly syndrome -- |
| -- |
Pseudo-Gaucher disease -- |
| -- |
Pseudoachondroplasia -- |
| -- |
Pseudoxanthoma elasticum -- |
| -- |
Pyloric stenosis -- |
| -- |
Pyruvate carboxylase deficiency -- |
| -- |
Pyruvate dehydrogenase complex deficiency -- |
| -- |
Pyruvate kinase deficiency -- |
| -- |
Raynaud disease -- |
| -- |
Refsum disease -- |
| -- |
Renal agenesis -- |
| -- |
Renal failure due to hypertension -- |
| -- |
Renpenning syndrome -- |
| -- |
Retinitis pigmentosa -- |
| -- |
Retinoblastoma -- |
| -- |
Rett syndrome -- |
| -- |
Rheumatoid arthritis -- |
| -- |
Rhizomelic chondrodysplasia punctata -- |
| -- |
Rhodopsin -- |
| -- |
Rieger syndrome -- |
| -- |
RNA (ribonucleic acid) -- |
| -- |
Roberts SC phocomelia -- |
| -- |
Robinow syndrome -- |
| -- |
Rothmund-Thomson syndrome -- |
| -- |
Rubinstein-Taybi syndrome -- |
| -- |
Russell-Silver syndrome -- |
| -- |
Saethre-Chotzen syndrome -- |
| -- |
Schinzel-Giedion syndrome -- |
| -- |
Schizophrenia -- |
| -- |
Schwartz-Jampel syndrome -- |
| -- |
Scleroderma -- |
| -- |
Sclerosing bone dysplasias -- |
| -- |
Scoliosis -- |
| -- |
Sebastian syndrome -- |
| -- |
Seckel syndrome -- |
| -- |
Septo-optic dysplasia -- |
| -- |
Severe combined immunodeficiency -- |
| -- |
Short-Rib polydactyly -- |
| -- |
Shprintzen-Goldberg craniosynostosis syndrome -- |
| -- |
Sickle cell disease -- |
| -- |
Simpson-Golabi-Behmel syndrome -- |
| -- |
Sirenomelia -- |
| -- |
Sjogren-Larsson syndrome -- |
| -- |
Skeletal dysplasia -- |
| -- |
Smith-Fineman-Myers syndrome -- |
| -- |
Smith-Lemli-Opitz syndrome -- |
| -- |
Smith-Magenis syndrome -- |
| -- |
Sotos syndrome -- |
| -- |
Spastic cerebral palsy -- |
| -- |
Spina bifida -- |
| -- |
Spinal muscular atrophy -- |
| -- |
Spinocerebellar ataxia -- |
| -- |
Spondyloepiphyseal dysplasia -- |
| -- |
Spondyloepiphyseal dysplasia congenita -- |
| -- |
SRY (Sex Determining Region Y) -- |
| -- |
Stargardt disease -- |
| -- |
Stickler syndrome -- |
| -- |
Sturge-Weber syndrome -- |
| -- |
Sutherland-Haan syndrome -- |
| -- |
angier disease -- |
| -- |
Tar syndrome -- |
| -- |
Tay-Sachs disease -- |
| -- |
Teratogen -- |
| -- |
Thalassemia -- |
| -- |
Thalidomide embryopathy -- |
| -- |
Thanatophoric dysplasia -- |
| -- |
Thrombasthenia of Glanzmann and Naegeli -- |
| -- |
Tomaculous neuropathy -- |
| -- |
Tourette syndrome -- |
| -- |
Treacher Collins syndrome -- |
| -- |
Trichorhinophalangeal syndrome -- |
| -- |
Triose phosphate isomerase deficiency -- |
| -- |
Triple X syndrome -- |
| -- |
Triploidy -- |
| -- |
Trismus-pseudocamptodactyly syndrome -- |
| -- |
Trisomy 8 mosaicism syndrome -- |
| -- |
Trisomy 13 -- |
| -- |
Trisomy 18 -- |
| -- |
Tuberous sclerosis complex -- |
| -- |
Turner syndrome -- |
| -- |
Urea cycle disorders -- |
| -- |
Urogenital adysplasia syndrome -- |
| -- |
Usher syndrome -- |
| -- |
Van der Woude syndrome -- |
| -- |
Vater association -- |
| -- |
Von Hippel-Lindau syndrome -- |
| -- |
Von Recklinghausen's neurofibromatosis -- |
| -- |
Von Willebrand disease -- |
| -- |
Waardenburg syndrome -- |
| -- |
Walker-Warburg syndrome -- |
| -- |
Weaver syndrome -- |
| -- |
Weissenbacher-Zweymuller syndrome -- |
| -- |
Werner syndrome -- |
| -- |
Williams syndrome -- |
| -- |
Wilson disease -- |
| -- |
Wiskott-Aldrich syndrome -- |
| -- |
Wolf-Hirschhorn syndrome -- |
| -- |
Wolman disease -- |
| -- |
X-linked hydrocephaly -- |
| -- |
X-linked mental retardation -- |
| -- |
X-linked severe combined immunodeficiency -- |
| -- |
Xeroderma pigmentosum -- |
| -- |
XXXX syndrome -- |
| -- |
XXXXX syndrome -- |
| -- |
XYY syndrome -- |
| -- |
YY syndrome -- |
| -- |
Zellweger syndrome -- |
| -- |
Zygote. |
| 520 ## - SUMMARY, ETC. |
|---|
| Summary, etc. |
Provides clear, complete information on genetic disorders, including conditions, tests, procedures, treatments and therapies, in articles that are both comprehensive and easy to understand in language accessible to laypersons. |
| 530 ## - COPYRIGHT INFORMATION: |
|---|
| COPYRIGHT INFORMATION |
COPYRIGHT NOT covered - Click this link to request copyright permission: |
| Uniform Resource Identifier |
<a href="b">b</a> |
| 588 ## - SOURCE OF DESCRIPTION NOTE |
|---|
| Source of description note |
Description based on print version record. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
|---|
| Topical term or geographic name entry element |
Medical genetics |
| Form subdivision |
Encyclopedias. |
| 650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
|---|
| Topical term or geographic name entry element |
Genetic disorders |
| Form subdivision |
Encyclopedias. |
| 700 1# - ADDED ENTRY--PERSONAL NAME |
|---|
| Personal name |
Fundukian, Laurie J., |
| Dates associated with a name |
1970- |
| Relator term |
|
| 710 2# - ADDED ENTRY--CORPORATE NAME |
|---|
| Corporate name or jurisdiction name as entry element |
Gale Group. |
| 776 08 - ADDITIONAL PHYSICAL FORM ENTRY |
|---|
| Relationship information |
Print version -- |
| Title |
|
| -- |
Gale encyclopedia of genetic disorders. |
| Place, publisher, and date of publication |
Farmington Hills, Mich. : Gale, c2011 |
| International Standard Book Number |
9781414476025 |
| Record control number |
(DLC) 2010002222 |
| 856 40 - ELECTRONIC LOCATION AND ACCESS |
|---|
| Uniform Resource Identifier |
<a href="https://link.gale.com/apps/pub/3FQF/GVRL?sid=gale_marc&u=columbiaiu">https://link.gale.com/apps/pub/3FQF/GVRL?sid=gale_marc&u=columbiaiu</a> |
| -- |
Available via Gale eBooks. Click here to access |
| 912 ## - |
|---|
| -- |
3FQF |
| 942 ## - ADDED ENTRY ELEMENTS (KOHA) |
|---|
| Source of classification or shelving scheme |
Library of Congress Classification |
| Usage before 2021-2022 |
CIU |
| Koha item type |
Online Book (LOGIN USING YOUR MY CIU LOGIN AND PASSWORD) |
| VENDOR |
GALE |
| LOCATION |
ONLINE |
| Barecode |
GALGVRL3FQF |
| 902 ## - LOCAL DATA ELEMENT B, LDB (RLIN) |
|---|
| a |
1 |
| b |
Cynthia Snell |
| c |
1 |
| d |
Cynthia Snell |