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07216aam a2200469 a 4500 001 79DB2DDA019E11E89C78220097128E48 003 SILO 005 20180125010234 008 050223t20062006njua b 000 0 eng 010 $a 2005005388 020 $a 9781592599561 020 $a 1592599567 020 $a 9781588296818 020 $a 1588296814 035 $a (OCoLC)57731393 040 $a DNLM/DLC $c DLC $d NLM $d BAKER $d MNY $d IaU $d UtOrBLW $d SILO 042 $a pcc 050 00 $a RB155.6 $b .A93 2006 060 00 $a 2006 A-709 060 10 $a QZ 17 $b A880383 2006 082 00 $a 616/.042 $2 22 100 1 $a Chen, Harold. $0 http://id.loc.gov/authorities/names/n88185852 245 10 $a Atlas of genetic diagnosis and counseling / $c Harold Chen. 264 1 $a Totowa, N.J. : $b Humana Press, $c [2006] 300 $a xi, 1,076 pages : $b illustrations ; $c 29 cm 504 $a Includes bibliographical references. 505 0 $a Arcadia -- Achondrogenesis -- Achondroplasia -- Adams-Oliver syndrome -- Agnathia -- Aicardi syndrome -- Alagille syndrome -- Albinism -- Amniotic band syndrome -- Androgen insensitivity syndrome -- Angelman syndrome -- Apert syndrome -- Aplasia cutis congenita -- Arthrogryposis multiplex congenita -- Asphyxiating thoracic dystrophy -- Ataxia telangiectasia -- Atelosteogenesis -- Autism -- Beckwith-Wiedemann syndrome -- Behcet disease -- Bladder exstrophy -- Body stalk anamoly -- Branchial clefts anamolies -- Campomelic dysplasia -- Cat eye syndrome -- Cerebro-costo-mandibular syndrome -- Charcot-Marie-Tooth disease -- CHARGE Association -- Cherubism -- Chiari malformation -- Chondrodysplasia punctata -- Chromosome abnormalities in pediatric solid tumors -- Cleft lip and/or cleft palate -- Cleidocranial dysplasia -- Cloacal exstrophy -- Collodion baby -- Congenital adrenal hyperplasia (21-hydroxylase deficiency) -- Congenital cutis laxa -- Congenital cytomegalovirus infection -- 505 80 $a Congenital generalized lipodystrophy -- Congenital hydrocephalus -- Congenital hypothyriodism -- Congenital muscular dystrophy -- Congenital toxoplasmosis -- Conjoined twins -- Corpus callosum agenesis/dysgenesis -- Craniometaphysical dysplasia -- Cri-du-chat syndrome -- Crouzon syndrome -- Cystic fibrosis -- Dandy-Walker malformation -- De Lange syndrome -- Del(22q11.2) syndromes -- Diabetic embryopathy -- Down syndrome -- Dyschondrosteosis (Leri-Weill Syndrome) and Langer Mesomelic dysplasia -- Dysmelia (limb deficiency/reduction) -- Dysplasia epiphysealis hemimelica -- Dystonia -- Dystrophinopathies -- Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome -- Dhlers-Danlos syndrome -- Ellis-van Creveld syndrome -- Enchondromatosis (Maffucci syndrome; Ollier syndrome) -- Epidermolysis bullosa -- Epidermolytic palmoplantar keratoderma -- Faciogenital (Aarskog) dysplasia -- Facioscapulohumeral muscular dystrophy -- Familial adenomatous polyposis -- Familial hyperlysinemia -- 505 80 $a Fanconi anemia -- Femoral hypoplasia-unusual facies syndrome -- Fetal akinesia syndrome -- Fetal alcohol syndrome -- Fibrodysplasia ossificans progressiva -- Finlay-Marks syndrome -- Fragile X syndrome -- Fraser syndrome -- Freeman-Sheldon syndrome -- Frontonasal dysplasia -- Galactosemia -- Gastroschisis -- Gaucher disease -- Generalized arterial calcification of infancy -- Glucose 6-phosphate dehydrogenase deficiency -- Glycogen storage disease, type II -- Goldenhar syndrome -- Hallermann-Streiff syndrome -- Harlequin ichthyosis (harlequin fetus) -- Hemophilia A -- Hereditary hemochromatosis -- Hereditary multiple exostoses -- Holoprosencephaly -- Holt-Oram syndrome -- Hydrops fetalis -- Hyper-IgE syndrome -- Hypochondroplasia -- Hypoglossia-hypodactylia syndrome -- Hypohidrotic ectodermal dysplasia -- Hypomelanosis of Ito -- Hypophosphatasia -- Incontinentia pigmenti -- Infantile myofibromatosis -- Ivemark syndrome -- Jarcho-Levin syndrome -- Kabuki syndrome -- 505 80 $a Kasabach-Merritt syndrome -- KID syndrome -- Klinefelter syndrome -- Klippel-Feil syndrome -- Klippel-Trenaunay syndrome -- Kniest dysplasia -- Larsen syndrome -- LEOPARD syndrome -- Lesch-Nyhan syndrome -- Lethal multiple pterygium syndrome -- Lowe syndrome -- Marfan syndrome -- McCune-Albright syndrome -- Meckel-Gruber syndrome -- Menkes disease (Kinky-hair syndrome) -- Metachromatic leukodystrophy -- Miller-Dieker syndrome -- MoÌbius syndrome -- Mucolipidosis II (I-cell disease) -- Mucolipidosis III (pseudo-Hurler polydystrophy) -- Mucopolysaccharidosis I (MPS I) (alpha-L-iduronidase deficiency) : Hurler (MPS I-H), Hurler-Scheie (MPS I-H/S), and Scheie (MPS I-S) syndromes -- Mucopolysaccharidosis II (Hunter syndrome) -- Mucopolysaccharidosis III (Sanfilippo syndrome) -- Mucopolysaccharidosis IV (Morquio syndrome) -- Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome) -- Multiple epiphyseal dysplasia -- Multiple pterygium syndrome -- Myotonic dystrophy type I -- Netherton syndrome -- 505 80 $a Neu-Laxova syndrome -- Neural tube defects -- Neurofibromatosis I -- Noonan syndrome -- Oblique facial cleft syndrome -- Oligohydramnios sequence -- Omphalocele -- Osteogenesis imperfecta -- Osteopetrosis -- Pachyonychia congenita -- Pallister-Killian syndrome -- Phenylketonuria (PKU) -- Pierre Robin sequence -- Polycystic kidney disease, autosomal dominant type -- Polycystic kidney disease, autosomal recessive type -- Prader-Willi syndrome -- Progeria -- Prune belly syndrome -- Pseudoachondroplasia -- R(18) syndrome -- Retinoid embyopathy -- Rett syndrome -- Rickets -- Roberts syndrome -- Robinow syndrome -- Rubinstein-Taybi syndrome -- Schizencephaly -- Schmid metaphyseal chondrodysplasia -- Seckel syndrome -- Severe combined immune deficiency -- Short rib polydactyly sydromes -- Sickle cell disease -- Silver-Russell syndrome -- Sirenomelia -- Smith-Lemli-Opitz syndrome -- Smith-Magenis syndrome -- Sotos syndrome -- Spinal muscular atrophy -- Spondyloepiphyseal dysplasia -- 505 80 $a Stickler syndrome -- Sturge-Weber syndrome -- Tay-Sachs disease -- Tetrasomy 9p syndrome -- Thalassemia -- Thanatophoric dysplasia -- Thrombocytopenia-absent radius syndrome -- Treacher-Collins syndrome -- Trimethylaminuria -- Triploidy -- Trismus pseudocamptodactyly syndrome -- Trisomy 13 syndrome -- Trisomy 18 syndrome -- Tuberous sclerosis -- Turner syndrome -- Twin-twin transfusion syndrome -- Ulnar-mammary syndrome -- VATER (VACTERL) Association -- Von Hippel-Lindau disease -- Waardenburg syndrome -- Williams syndrome -- Wolf-Hirschhorn syndrome -- X-linked ichthyosis -- XXX syndrome -- XXXXX syndrome -- XXXXY syndrome -- XY female -- XYY syndrome. 650 0 $a Genetic disorders $x Diagnosis $v Atlases. 650 0 $a Genetic counseling $v Atlases. 650 12 $a Genetic Diseases, Inborn. $2 [MeSH] $0 https://id.nlm.nih.gov/mesh/D030342 650 22 $a Genetic Counseling. $2 [MeSH] $0 https://id.nlm.nih.gov/mesh/D005817 650 22 $a Prenatal Diagnosis. $2 [MeSH] $0 https://id.nlm.nih.gov/mesh/D011296 655 2 $a Atlases. 655 7 $a Atlases. $2 lcgft $0 http://id.loc.gov/authorities/genreForms/gf2011026058 941 $a 1 952 $l OVUX522 $d 20231019024503.0 956 $a http://locator.silo.lib.ia.us/search.cgi?index_0=id&term_0=79DB2DDA019E11E89C78220097128E48Initiate Another SILO Locator Search