000			14573cam a2200469 i 4500
001			GVRL3FQF
003			MiFhGG
005			20241102175636.0
006			m o d
007			cr un ---uuuua
008			100119s2011 miua obe 001 0 eng d
020			_a9781414476056 _q(electronic book)
035			_a(OCoLC)611868396
040			_aMiFhGG _beng _cMiFhGG _erda _epn
050		4	_aRB155.5
060	0	0	_aQZ 13 _bG1517 2011
245	0	4	_aThe Gale encyclopedia of genetic disorders / _cLaurie J. Fundukian, editor.
246	1	3	_aEncyclopedia of genetic disorders
246	1	3	_aGenetic disorders
250			_a3rd edition.
264		1	_aFarmington Hills, Mich. : _bGale, _c[(c)2011.]
300			_a1 online resource (2 volumes) : _bcolor illustrations
336			_atext _btxt _2rdacontent
337			_acomputer _bc _2rdamedia
338			_aonline resource _bcr _2rdacarrier
347			_adata file _2rda
490	0		_aGale eBooks
504			_a2
505	0		_a22q13 deletion syndrome -- _tAarskog syndrome -- _tAase syndrome -- _tAbetalipoproteinemia -- _tAbsence of vas deferens -- _tAcardia -- _tAccutane embryopathy -- _tAceruloplasminemia -- _tAchondrogenesis -- _tAchondroplasia -- _tACHOO syndrome -- _tAcrocallosal syndrome -- _tAcromegaly -- _tAdams-Oliver syndrome -- _tAdelaide-type craniosynostosis -- _tAdenylosuccinate lyase deficiency -- _tAdrenoleukodystrophy -- _tAicardi syndrome -- _tAla dehydratase deficiency -- _tAlagille syndrome -- _tAlbinism -- _tAlcoholism -- _tAlexander disease -- _tAlkaptonuria -- _tAlpha-1 antitrypsin -- _tAlpha-thalassemia X-linked mental retardation syndrome -- _tAlstrom syndrome -- _tAlzheimer's disease -- _tAmelia -- _tAmelogenesis imperfecta -- _tAmniocentesis -- _tAmyoplasia -- _tAmyotrophic lateral sclerosis -- _tAndrogen insensitivity syndrome -- _tAnemia, sideroblastic X-linked -- _tAnencephaly -- _tAngelman syndrome -- _tAnkylosing spondylitis -- _tApert syndrome -- _tArginase deficiency -- _tArnold-Chiari malformation -- _tArthrogryposis multiplex congenita -- _tArthropathy-camptodactyly syndrome -- _tAsperger syndrome -- _tAsplenia -- _tAsthma -- _tAstrocytoma -- _tAttention deficit hyperactivity disorder -- _tAutism -- _tAzorean disease -- _tBardet-biedl syndrome -- _tBarth syndrome -- _tBassen-Kornzweig syndrome -- _tBatten disease -- _tBeals disease -- _tBeare-Stevenson cutis gyrata syndrome -- _tBeckwith-Wiedemann syndrome -- _tBeta thalassemia -- _tBicuspid aortic valve -- _tBiotinidase deficiency -- _tBipolar disorder -- _tBirt-Hogg-Dube syndrome -- _tBloom syndrome -- _tBlue rubber bleb nevus syndrome -- _tBrachydactyly -- _tBranchiootorenal syndrome -- _tBreast cancer -- _tBruton agammaglobulinemia -- _tBurger-Grutz syndrome -- _tCampomelic dysplasia -- _tCanavan disease -- _tCancer -- _tCancer genetics -- _tCardiofaciocutaneous syndrome -- _tCarnitine palmitoyltransferase deficiency -- _tCarpenter syndrome -- _tCaudal dysplasia -- _tCayler cardiofacial syndrome -- _tCeliac disease -- _tCentral core disease -- _tCerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy -- _tCerebral palsy -- _tChannelopathies -- _tCharcot-Marie-Tooth disease -- _tCharge syndrome -- _tChediak-Higashi syndrome -- _tChondrodysplasia punctata -- _tChondrosarcoma -- _tChoroideremia -- _tChromosomal abnormalities -- _tChromosome -- _tChromosome map -- _tCleft lip and palate -- _tCleidocranial dysplasia -- _tClubfoot -- _tCockayne syndrome -- _tCoffin-Lowry syndrome -- _tCoffin-Siris syndrome -- _tCohen syndrome -- _tCollagenopathy, types II and XI -- _tColoboma -- _tColor blindness -- _tCompression neuropathy -- _tCone-Rod dystrophy -- _tCongenital adrenal hyperplasia -- _tCongenital heart disease -- _tCongenital hypothyroid syndrome -- _tCongenital methemoglobinemia -- _tConjoined twins -- _tConotruncal anomaly face syndrome -- _tCorneal dystrophy -- _tCornelia de lange syndrome -- _tCorpus callosum, agenesis -- _tCostello syndrome -- _tCowden syndrome -- _tCrane-Heise syndrome -- _tCraniosynostosis -- _tCri du chat syndrome -- _tCrouzon syndrome -- _tCrouzonodermoskeletal syndrome -- _tCystic fibrosis -- _tCystinosis -- _tCystinuria -- _tDandy-walker malformation -- _tDe Grouchy syndrome -- _tDeletion 22q11 syndrome -- _tDementia -- _tDentatorubral-pallidoluysian atrophy -- _tDent's disease -- _tDepression -- _tDiabetes -- _tDiastrophic dysplasia -- _tDistal arthrogryposis syndrome -- _tDNA (deoxyribonucleic acid) -- _tDonohue syndrome -- _tDown syndrome -- _tDuane retraction syndrome -- _tDubowitz syndrome -- _tDuchenne muscular dystrophy -- _tDyschondrosteosis -- _tDysplasia -- _tDystonia -- _tEctodermal dysplasia -- _tEctrodactyly-ectodermal dysplasia-clefting syndrome -- _tEhlers-Danlos syndrome -- _tEllis-van Creveld syndrome -- _tEmery-Dreifuss muscular dystrophy -- _tEncephalocele -- _tEngelmann disease -- _tEntrapment neuropathy -- _tEpidermolysis bullosa -- _tEpilepsy -- _tErythropoietic porphyria -- _tErythropoietic protoporphyria -- _tEssential hypertension -- _tEssential tremor -- _tFabry disease -- _tFacioscapulohumeral muscular dystrophy -- _tFactor V Leiden thrombophilia -- _tFahr disease -- _tFamilial adenomatous polyposis -- _tFamilial dysautonomia -- _tFamilial Mediterranean fever -- _tFamilial nephritis -- _tFamilial pulmonary arterial hypertension -- _tFanconi anemia -- _tFanconi-Bickel syndrome -- _tFetal alcohol syndrome -- _tFG syndrome -- _tFibroblast growth factor receptor mutations -- _tFluorescent in situ hybridization -- _tFragile x syndrome -- _tFraser syndrome -- _tFreeman-Sheldon syndrome -- _tFriedreich ataxia -- _tFrontonasal dysplasia -- _tFrontotemporal dementia -- _tFryns syndrome -- _tGalacktokinase deficiency -- _tGalactosemia -- _tGastric cancer -- _tGastroschisis -- _tGaucher disease -- _tGene -- _tGene mutations -- _tGene pool -- _tGene therapy -- _tGenetic counseling -- _tGenetic disorders -- _t-- Genetic mapping -- _tGenetic testing -- _tGenetics and congenital anomalies -- _tGenitalia, ambiguous -- _tGenome -- _tGenome sequencing -- _tGenotype and phenotype -- _tGerstmann-Straussler-Scheinker disease -- _tGlaucoma -- _tGlycogen storage diseases -- _tGoltz syndrome -- _tGM1-gangliosidosis -- _tGreig cephalopolysyndactyly -- _tGriscelli syndrome -- _tHaim-Munk syndrome -- _tHair loss syndromes -- _tHallermann-Streiff syndrome -- _tHand-foot-uterus syndrome -- _tHarlequin fetus -- _tHemifacial microsomia -- _tHemihypertrophy (hemihyperplasia) -- _tHemochromatosis -- _tHemolytic-uremic syndrome -- _tHemophilia -- _tHepatocellular carcinoma -- _tHerceptin -- _tHereditary angioneurotic edema -- _tHereditary colorectal cancer -- _tHereditary coproporphyria -- _tHereditary desmoid disease -- _tHereditary hearing loss and deafness -- _tHereditary multiple exostoses -- _tHereditary nonpolyposis colorectal cancer -- _tHereditary pancreatitis -- _tHereditary spastic paraplegia -- _tHereditary spherocytosis -- _tHermansky-Pudlak syndrome -- _tHermaphroditism -- _tHirschsprung disease -- _tHoloprosencephaly -- _tHolt-Oram syndrome -- _tHomocystinuria -- _tHuman genome project -- _tHuntington disease -- _tHydrocephalus -- _tHydrolethalus syndrome -- _tHydrops fetalis -- _tHyperlipoproteinemia -- _tHyperoxaluria -- _tHyperphenylalaninemia -- _tHypochondrogenesis -- _tHypochondroplasia -- _tHypophosphatasia -- _tHypophosphatemia -- _tHypospadias and epispadias -- _tIchthyosis -- _tImprinting -- _tIncontinentia pigmenti -- _tInfantile Refsum disease -- _tInheritance -- _tInherited arrhythmia --
505	8		_aJackson-Weiss syndrome -- _tJacobsen syndrome -- _tJervell and Lange-Nielsen syndrome -- _tJoubert syndrome -- _tKabuki syndrome -- _tKallmann syndrome -- _tKartagener syndrome -- _tKaryotype -- _tKennedy disease -- _tKlinefelter syndrome -- _tKlippel-Feil syndrome -- _tKlippel-Trenaunay-Weber syndrome -- _tKniest dysplasia -- _tKrabbe disease -- _tLanger-Saldino achondrogenesis -- _tLarsen syndrome -- _tLaterality sequence -- _tLeber congenital amaurosis -- _tLebers hereditary optic atrophy -- _tLeigh syndrome -- _tLesch-Nyhan syndrome -- _tLeukodystrophy -- _tLi-Fraumeni syndrome -- _tLimb-girdle muscular dystrophy -- _tLipoprotein lipase deficiency -- _tLissencephaly -- _tLong QT syndrome -- _tLowe oculocerebrorenal syndrome -- _tMachado-Joseph disease -- _tMacular degeneration, age-related -- _tMajor histocompatibility complex -- _tMalignant hyperthermia -- _tMannosidosis -- _tMarfan syndrome -- _tMarshall syndrome -- _tMarshall-Smith syndrome -- _tMCAD deficiency -- _tMcCune-Albright syndrome -- _tMcKusick-Kaufman syndrome -- _tMeckel-Gruber syndrome -- _tMeckel's diverticulum -- _tMenkes syndrome -- _tMetaphyseal dysplasia -- _tMethylmalonic acidemia -- _tMethylmalonicaciduria due to methylmalonic CoA mutase deficiency -- _tMicro syndrome -- _tMicrocephaly (childhood) -- _tMicrophthalmia with linear skin defects (MLS) -- _tMiller-Dieker syndrome -- _tMoebius syndrome -- _tMonosomy 1p36 syndrome -- _tMowat-Wilson syndrome -- _tMoyamoya -- _tMucolipidosis -- _tMucopolysaccharidoses -- _tMucopolysaccharidosis type I, Mucopolysaccharidosis type II -- _tMuir-Torre syndrome -- _tMultifactorial inheritance -- _tMultiple endocrine neoplasias -- _tMultiple epiphyseal dysplasia -- _tMultiple lentigines syndrome -- _tMultiple sclerosis -- _tMultiplex ligation-dependent probe amplification -- _tMuscular dystrophy -- _tMyasthenia gravis -- _tMyopia -- _tMyotonic dystrophy -- _tMyotubular myopathy -- _tNail-patella syndrome -- _tNance-Insley syndrome -- _tNarcolepsy -- _tNephrogenic diabetes insipidus -- _tNeu-Laxova syndrome -- _tNeural tube defects -- _tNeuraminidase deficiency -- _tNeuraminidase deficiency with beta-galactosidase deficiency -- _tNeurofibromatosis -- _tNevoid basal cell carcinoma -- _tNiemann-Pick disease -- _tNijmegen breakage syndrome -- _tNonketotic hyperglycemia -- _tNoonan syndrome -- _tNorrie disease -- _tOculo-digito-esophago-duodenal syndrome -- _tOculodentodigital syndrome -- _tOligohydramnios sequence -- _tOmphalocele -- _tOncogene -- _tOpitz syndrome -- _tOral-facial-digital syndrome -- _tOrganic acidemias -- _tOrnithine transcarbamylase deficiency -- _tOsler-Weber-Rendu syndrome -- _tOsteoarthritis -- _tOsteogenesis imperfecta -- _tOsteoporosis -- _tOsteosarcoma -- _tOtopalatodigital syndrome -- _tOvarian cancer -- _tPaine syndrome -- _tPallister-Hall syndrome -- _tPallister Killian syndrome -- _tPancreatic beta cell agenesis -- _tPancreatic cancer -- _tPanic disorder -- _tPantothenate kinase-associated neurodegeneration (PKAN) -- _tParkinson disease -- _tParoxysmal nocturnal hemoglobinuria -- _tPatent ductus arteriosus -- _tPedigree analysis -- _tPelizaeus-Merzbacher disease -- _tPendred syndrome -- _tPervasive developmental disorders -- _tPeutz-Jeghers syndrome -- _tPfeiffer syndrome -- _tPharmacogenetics -- _tPhenylketonuria -- _tPierre-Robin sequence -- _tPituitary dwarfism -- _tPoland anomaly -- _tPolycystic kidney disease -- _tPolycystic ovary syndrome -- _tPolydactyly -- _tPompe disease -- _tPorphyrias -- _tPrader-Willi syndrome -- _tPrenatal ultrasound -- _tPrion diseases -- _tProgeria syndrome -- _tPropionic acidemia -- _tProstate cancer -- _tProtein C deficiency -- _tProtein S deficiency -- _tProteus syndrome -- _tPrune-Belly syndrome -- _tPseudo-Gaucher disease -- _tPseudoachondroplasia -- _tPseudoxanthoma elasticum -- _tPyloric stenosis -- _tPyruvate carboxylase deficiency -- _tPyruvate dehydrogenase complex deficiency -- _tPyruvate kinase deficiency -- _tRaynaud disease -- _tRefsum disease -- _tRenal agenesis -- _tRenal failure due to hypertension -- _tRenpenning syndrome -- _tRetinitis pigmentosa -- _tRetinoblastoma -- _tRett syndrome -- _tRheumatoid arthritis -- _tRhizomelic chondrodysplasia punctata -- _tRhodopsin -- _tRieger syndrome -- _tRNA (ribonucleic acid) -- _tRoberts SC phocomelia -- _tRobinow syndrome -- _tRothmund-Thomson syndrome -- _tRubinstein-Taybi syndrome -- _tRussell-Silver syndrome -- _tSaethre-Chotzen syndrome -- _tSchinzel-Giedion syndrome -- _tSchizophrenia -- _tSchwartz-Jampel syndrome -- _tScleroderma -- _tSclerosing bone dysplasias -- _tScoliosis -- _tSebastian syndrome -- _tSeckel syndrome -- _tSepto-optic dysplasia -- _tSevere combined immunodeficiency -- _tShort-Rib polydactyly -- _tShprintzen-Goldberg craniosynostosis syndrome -- _tSickle cell disease -- _tSimpson-Golabi-Behmel syndrome -- _tSirenomelia -- _tSjogren-Larsson syndrome -- _tSkeletal dysplasia -- _tSmith-Fineman-Myers syndrome -- _tSmith-Lemli-Opitz syndrome -- _tSmith-Magenis syndrome -- _tSotos syndrome -- _tSpastic cerebral palsy -- _tSpina bifida -- _tSpinal muscular atrophy -- _tSpinocerebellar ataxia -- _tSpondyloepiphyseal dysplasia -- _tSpondyloepiphyseal dysplasia congenita -- _tSRY (Sex Determining Region Y) -- _tStargardt disease -- _tStickler syndrome -- _tSturge-Weber syndrome -- _tSutherland-Haan syndrome -- _tangier disease -- _tTar syndrome -- _tTay-Sachs disease -- _tTeratogen -- _tThalassemia -- _tThalidomide embryopathy -- _tThanatophoric dysplasia -- _tThrombasthenia of Glanzmann and Naegeli -- _tTomaculous neuropathy -- _tTourette syndrome -- _tTreacher Collins syndrome -- _tTrichorhinophalangeal syndrome -- _tTriose phosphate isomerase deficiency -- _tTriple X syndrome -- _tTriploidy -- _tTrismus-pseudocamptodactyly syndrome -- _tTrisomy 8 mosaicism syndrome -- _tTrisomy 13 -- _tTrisomy 18 -- _tTuberous sclerosis complex -- _tTurner syndrome -- _tUrea cycle disorders -- _tUrogenital adysplasia syndrome -- _tUsher syndrome -- _tVan der Woude syndrome -- _tVater association -- _tVon Hippel-Lindau syndrome -- _tVon Recklinghausen's neurofibromatosis -- _tVon Willebrand disease -- _tWaardenburg syndrome -- _tWalker-Warburg syndrome -- _tWeaver syndrome -- _tWeissenbacher-Zweymuller syndrome -- _tWerner syndrome -- _tWilliams syndrome -- _tWilson disease -- _tWiskott-Aldrich syndrome -- _tWolf-Hirschhorn syndrome -- _tWolman disease -- _tX-linked hydrocephaly -- _tX-linked mental retardation -- _tX-linked severe combined immunodeficiency -- _tXeroderma pigmentosum -- _tXXXX syndrome -- _tXXXXX syndrome -- _tXYY syndrome -- _tYY syndrome -- _tZellweger syndrome -- _tZygote.
520			_aProvides 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			_a2 _ub
588			_aDescription based on print version record.
650		0	_aMedical genetics _vEncyclopedias.
650		0	_aGenetic disorders _vEncyclopedias.
700	1		_aFundukian, Laurie J., _d1970- _eeditor.
710	2		_aGale Group.
776	0	8	_iPrint version -- _t _tGale encyclopedia of genetic disorders. _dFarmington Hills, Mich. : Gale, c2011 _z9781414476025 _w(DLC) 2010002222
856	4	0	_uhttps://link.gale.com/apps/pub/3FQF/GVRL?sid=gale_marc&u=columbiaiu _zAvailable via Gale eBooks. Click here to access
912			_a3FQF
942			_2lcc _bCIU _cOB _eGAL _QOL _zGALGVRL3FQF
999			_c105256 _d105256
902			_a1 _bCynthia Snell _c1 _dCynthia Snell