Description
HUMANA PRESS Atlas Of Genetic Diagnosis And Counseling by CHEN
The Atlas of Genetic Diagnosis and Counseling on CD-ROM provides instant access to over 200 genetic disorders, malformations, and malformation systems. This easy-to-use CD-ROM contains over 650 High Resolution Color Images, is fully searchable, and also features references that link out to PubMed. Portable and fully compatible with PC and Mac formats, The Atlas of Genetic Diagnosis and Counseling on CD-ROM is a must have for all physicians in the field. Also available in a Hardcover edition (ISBN: 1-58829-681-4). AcardiaAchondrogenesisAchondroplasiaAdams-Oliver SyndromeAgnathiaAicardi SyndromeAlagille SyndromeAlbinismAmniotic Band SyndromeAndrogen Insensitivity SyndromeAngelman SyndromeApert SyndromeAplasia Cutis CongenitaArthrogryposis Multiplex CongenitaAsphyxiating Thoracic DystrophyAtaxia TelangiectasiaAtelosteogenesisAutismBeckwith-Wiedemann SyndromeBehcet DiseaseBladder ExstrophyBody Stalk AnomalyBranchial Cleft AnomaliesCampomelic DysplasiaCat Eye SyndromeCerebro-Costo-Mandibular SyndromeCharcot-Marie-Tooth DiseaseCHARGE AssociationCherubismChiari MalformationChondrodysplasia PunctataChromosome Abnormalities in Pediatric Solid TumorsCleft Lip and/or Cleft PalateCleidocranial DysplasiaCloacal ExstrophyCollodion BabyCongenital Adrenal Hyperplasia (21-Hydroxylase Deficiency)Congenital Cutis LaxaCongenital Cytomegalovirus InfectionCongenital Generalized LipodystrophyCongenital HydrocephalusCongenital HypothyroidismCongenital Muscular DystrophyCongenital ToxoplasmosisConjoined TwinsCorpus Callosum Agenesis/DysgenesisCraniometaphyseal DysplasiaCri-Du-Chat SyndromeCrouzon SyndromeCystic FibrosisDandy-Walker MalformationDe Lange SyndromeDel(22q11.2) SyndromesDiabetic EmbryopathyDown SyndromeDyschondrosteosis (Leri-Weill Syndrome) and Langer Mesomelic DysplasiaDysmelia (Limb Deficiency/Reduction)Dysplasia Epiphysealis HemimelicaDystoniaDystrophinopathiesEctrodactyly-Ectodermal Dysplasia-Clefting (EEC) SyndromeEhlers-Danlos SyndromeEllis-van Creveld SyndromeEnchondromatosis (Maffucci Syndrome; Ollier Syndrome)Epidermolysis BullosaEpidermolytic Palmoplantar KeratodermaFaciogenital (Aarskog) DysplasiaFacioscapulohumeral Muscular DystrophyFamilial Adenomatous PolyposisFamilial HyperlysinemiaFanconi AnemiaFemoral Hypoplasia-Unusual Facies SyndromeFetal Akinesia SyndromeFetal Alcohol SyndromeFetal Hydantoin SyndromeFibrodysplasia Ossificans ProgressivaFinlay-Marks SyndromeFragile X SyndromeFraser SyndromeFreeman-Sheldon SyndromeFrontonasal DysplasiaGalactosemiaGastroschisisGaucher DiseaseGeneralized Arterial Calcification of InfancyGlucose-6-Phosphate Dehydrogenase DeficiencyGlycogen Storage Disease, Type IIGoldenhar SyndromeHallermann-Streiff SyndromeHarlequin Ichthyosis (Harlequin Fetus)Hemophilia AHereditary HemochromatosisHereditary Multiple ExostosesHoloprosencephalyHolt-Oram SyndromeHydrops FetalisHyper-IgE SyndromeHypochondroplasiaHypoglossia-Hypodactylia SyndromeHypohidrotic Ectodermal DysplasiaHypomelanosis of ItoHypophosphatasiaIncontinentia PigmentiInfantile MyofibromatosisIvemark SyndromeJarcho-Levin SyndromeKabuki SyndromeKasabach-Merritt SyndromeKID SyndromeKlinefelter SyndromeKlippel-Feil SyndromeKlippel-Trenaunay SyndromeKniest DysplasiaLarsen SyndromeLEOPARD SyndromeLesch-Nyhan SyndromeLethal Multiple Pterygium SyndromeLowe SyndromeMarfan SyndromeMcCune-Albright SyndromeMeckel-Gruber SyndromeMenkes Disease (Kinky-Hair Syndrome)Metachromatic LeukodystrophyMiller-Dieker SyndromeMoebius SyndromeMucolipidosis II (I-Cell Disease)Mucolipidosis III (Pseudo-Hurler Polydystrophy)Mucopolysaccharidosis I (MPS I) (a-L-Iduronidase Deficiency): Hurler (MPS I-H), Hurler-Scheie (MPS I-H/S), and Scheie (MPS I-S) SyndromesMucopolysaccharidosis II (Hunter Syndrome)Mucopolysaccharidosis III (Sanfilippo Syndrome)Mucopolysaccharidosis IV (Morquio Syndrome)Mucopolysaccharidosis VI (Maroteaux-Lamy Syndrome)Multiple Epiphyseal DysplasiaMultiple Pterygium SyndromeMyotonic Dystrophy Type 1Netherton SyndromeNeu-Laxova SyndromeNeural Tube DefectsNeurofibromatosis INoonan SyndromeOblique Facial Cleft SyndromeOligohydramnios SequenceOmphaloceleOsteogenesis ImperfectaOsteopetrosisPachyonychia CongenitaPallister-Killian SyndromePhenylketonuria (PKU)Pierre Robin SequencePolycystic Kidney Disease, Autosomal Dominant TypePolycystic Kidney Disease, Autosomal Recessive TypePrader-Willi SyndromeProgeriaPrune Belly SyndromePseudoachondroplasiaR(18) SyndromeRetinoid EmbryopathyRett SyndromeRicketsRoberts SyndromeRobinow SyndromeRubinstein-Taybi SyndromeSchizencephalySchmid Metaphyseal ChondrodysplasiaSeckel SyndromeSevere Combined Immune DeficiencyShort Rib Polydactyly SyndromesSickle Cell DiseaseSilver-Russell SyndromeSirenomeliaSmith-Lemli-Opitz SyndromeSmith-Magenis SyndromeSotos SyndromeSpinal Muscular AtrophySpondyloepiphyseal DysplasiaStickler SyndromeSturge-Weber SyndromeTay-Sachs DiseaseTetrasomy 9p SyndromeThalassemiaThanatophoric DysplasiaThrombocytopenia-Absent Radius SyndromeTreacher-Collins SyndromeTrimethylaminuriaTriploidyTrismus Pseudocamptodactyly SyndromeTrisomy 13 SyndromeTrisomy 18 SyndromeTuberous SclerosisTurner SyndromeTwin-Twin Transfusion SyndromeUlnar-Mammary SyndromeVATER (VACTERL) AssociationVon Hippel-Lindau DiseaseWaardenburg SyndromeWilliams SyndromeWolf-Hirschhorn SyndromeX-Linked IchthyosisXXX SyndromeXXXXX SyndromeXXXXY SyndromeXY FemaleXYY Syndrome