The Locator -- [(subject = "Prenatal Diagnosis")]

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08326cam a22005414a 4500
001 CCAC9DAE6BF311DEA13FF332A8D7520A
003 SILO
005 20100201083435
006 m        u        
007 co cgu---uuuuu
008 070208s2008    paua     b    001 0 eng  
010    $a 2007005669
020    $a 0443066418
020    $a 9780443066412
035    $a (OCoLC)84730246
040    $a DNLM/DLC $c DLC $d SILO $d BAKER $d BTCTA $d YDXCP $d C#P $d UKM $d UMM $d IG# $d Y4Q $d SILO
042    $a pcc
050 10 $a RG628.3.U58 $b B46 2008
060 00 $a 2008 B-161
060 10 $a WQ 211 $b B456u 2008
082 00 $a 618.3/207543 $2 22
100 1  $a Benacerraf, Beryl R.
245 1  $a Ultrasound of fetal syndromes / $c Beryl R. Benacerraf.
250    $a 2nd ed.
260    $a Philadelphia : $b Churchill Livingstone / Elsevier, $c c2008.
300    $a xvi, 650 p. : $b ill. (some col.) ; $c 29 cm. + $e 1 DVD-ROM (4 3/4 in.)
504    $a Includes bibliographical references and index.
505 0  $a Differntial dianoses. Cataract -- Microphthalmia/anophthalmia (unilateral or bilateral) -- Hypotelorism/cyclopia (extreme) -- Hypertelorism -- Choanal atresia -- Micrognathia -- Facial asymmetry -- Nasal bone hypoplasia (otherwise normal nose) -- Facial cleft -- Ear anomalies -- Abnormal head shape -- Sluid collections in the head -- Intracranial cyst -- Ventriculomegaly -- Macrocephaly -- Microcephaly -- Agenesis of the corpus callosum -- Dandy-Walker cyst or vermian hypoplasia -- Echogenic mass in the head -- Holoprosencephaly -- Neural tube defect -- Short spine -- Vertebral body segmental abnormalities (other than platyspondyly) -- Platyspondyly -- Rib abnormalities -- Mass on the surface of the fetus -- Nuchal membrane -- Nuchal thickening/cystic hygroma (first and/or second trimesters) -- Anterior abdominal wall defects -- Omphalocele -- Anterior neck mass -- Rotation of the heart -- Intrathoracic mass -- Diaphragmatic hernia -- Narrow chest -- Abdominal fluid collection or cyst -- Hyperechoic bowel -- Echogenic mass in abdomen -- Bowel obstruction -- Ascites -- Absent stomach -- Hydronephrosis -- Renal agenesis (unilateral or bilateral) -- Syndromes associated with various renal anomalies -- Absent bladder -- Distended bladder -- Suprarenal mass -- Enlarged kidneys -- GEnital anomalies -- Contractures of the extremities -- Clenched hands -- Polydactyly -- Clinodactyly -- Asymmetric lengths of extremities -- Slightly short femur -- Generalized short and bowed limbs -- Asymmetric limb reduction defects -- Short radial ray -- Club feet -- Rockerbottom feet -- Flared metaphyses or epithyses -- under-ossification of bone -- Cord cyst/mass -- Hydrops -- Decreased fetal activity -- Intrauterine growth restriction -- Enlarged placenta -- Polyhydramnios -- Oligohyframnios -- Heart defects -- Echogenic intracardiac focus -- Abnormal heart appearance --
505 0  $a Enlarged right side of hte heart (compared with the left) -- Smaller right side of the heart (compared with the left) -- Enlarged left side of the heart (compared with the right) -- Smaller left side of the heart (compared with the right) -- Single great vessel -- Single ventricle -- Syndromes. Syndromes featuring growth restriction. Cornelia de Lange syndrome -- Noonan syndrome -- Russell-Silver syndrome -- Seckel syndrome -- Smith-Lemli-Opitz sydrome -- Syndromes featuring fetal overgrowth. Beckwith-Wiedermann syndrome -- Maternal diabetes -- Perlman syndrome -- Syndromes featuring primarily facial anomalies. Branchio-ocular-facial syndrome -- Cataracts -- Cerebrocostomandibular syndrome -- Cleft lip and palate -- Fraser syndrome -- Goldenhar syndrome -- Medial cleft face syndrome -- Microphthalmia/anophthalmia -- Nager syndrome -- Oral-facial-digital syndrome, type I (OFD1) -- Oral-facial-digital syndrome, type II (Mohr syndrome) -- Pierre Robin syndrome -- Shprintzen syndrome -- Strickler syndrome -- Treacher Collins syndrome -- Van der Woude syndrome -- Syndromes featuring primarily brain anomalies. Aicardia syndrome -- Gorlin syndrome -- Hydrolethalis -- Joubert syndrome -- Meckel-Gruber syndrome -- Microcephaly -- Miller-Dieker syndrome (lissencephaly, type I) -- Neu-Laxova syndrome -- Septo-optic syndrome -- Walkter-Warburg syndrome -- X-linked hydrocephalus syndrome -- Limb abnormalities. Adams-Oliver syndrome -- Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome -- Fanconi anemia -- Femoral hyopplasi-unusual facies syndrome -- Femur-fibula-ulna (FFU) syndrome -- Freeman-Sheldon (whistling face) syndrome -- Holt-oram syndrome --
505 0  $a Larsen syndrome -- Multiple pterygium syndrome (lethal type) -- Roberts' syndrome -- Thrombocytopenia-absent radius (TAR) syndrome -- Skeletal dysplasias. Achondrogenesis -- Achodroplasia -- Atelosteogenesis, type I -- Camptomelic dysplasia -- Chondrodysplasia punctata -- Cleidocranial dysostosis -- Diastrophic dysplasia -- Ellis-van Creveld syndrome -- Hypochondroplasia -- Hypophosphatasia of the lethal type -- Jeune thoracic dystrophy -- Kniest syndrome -- Majewski syndrome -- Metatrophic dysplasia -- Osteopetrosis (lethal type) -- Short rib-polydactyly syndromes (SRPS) types I (Saldino-Noonan) and III (Naumoff) -- Spondyloepiphyseal dysplasia congenita -- Thanatophoric dysplasia -- Syndromes featuring primarily craniosynostosis. Antley-bixter syndrome -- Apert syndrome -- Carpenter syndrome -- Couzon syndrome -- Pfeiffer syndrome -- Saethre-Chotzen syndrome -- Miscellaneous syndromes. Cystic fibrosis -- Fryns syndrome -- Infantile polycystic kidney disease -- Jarcho-Levin syndrome -- Syndromes featuring primarily soft-tissue anomalies. Alpha-thalassernia -- Aplasia cutis congenita (ACC) -- Harlequin syndrome -- Klippel-Trenaunay-Weber syndrome -- Marfan syndrome -- Osteogenesis imperfecta -- Proteus syndrome -- Tuberous syndrome -- Sequence and associations. Amniotic band sequence -- Arthrogryposis -- Cardiosplenic syndromes (asplenia/polyspenia; heterotaxy) -- Caudal regression syndrome and sirenomelia -- Cerebro-occulo-facio-skeletal (CODS) syndrome -- CHARGE association -- Congenital adrenal hyperplasia -- Congenital high airway obstruction syndrome (CHAOS) -- Cloacal extrophy sequence -- Holoprosencephaly sequence -- Idiopathic arterial calcification of infancy --
505 0  $a Klippel-Feil syndrome -- MURCS association -- Opitz syndrome -- Pena Shokeir syndrome -- Pentalogy of cantrell -- Prune-belly syndrome -- Renal agenesis (Potter syndrome) -- Scimitar syndrome -- Spinal dysraphism -- VATER association -- Teratogens. Antibiotics -- Anticancer agents -- Anticoagulants -- Anticonvulsant drugs -- Anithyroid agents -- Hormones -- Tranquilizers and antidepressants -- Miscellaneous -- Maternal infections -- Syndromes featuring chromosomal anomalies. Cri-du-chat (distal 5p deletion syndrome) -- Deletion 4p (Wolf-Hirschhorn syndrome) -- Deletion 11q (Jacobsen syndrome) -- DiGeorge syndrome -- Tetrasomy (Pallister-Killiam syndrome) -- Triploidy -- Trisomy 9 -- Trisomy 10 -- Trisomy 13 (Patau syndrome) -- Trisomy 18 (Edwards syndrome) -- Trisomy 21 (downs syndrome) -- Trisomy 22 -- XO syndrome (Turner syndrome) -- Tumors. Cystic hygroma/lymphangioma -- Hemangioma -- Neuroblastoma -- Teratoma
538    $a System requirements for accompanying DVD-ROM Microsoft Windows: Windows 2000, XO, or Vista; 800 x 600 pixels screen resolution; 16.7 millions of colors; 256 MB RAM; P III 500 Mhz processor; DVD-ROM drive
538    $a System requirements for accompanying DVD-ROM Macintosh: OS X 10.2 or above, 800 x 600 pixels screen resolution, millions of colors, 256 MB RAM, G3 800 Mhz processor, DVD-ROM drive
650  0 $a Fetus $x Ultrasonic imaging.
650  0 $a Fetus $x Diagnosis. $x Diagnosis.
650  0 $a Fetus $x Diagnosis. $x Diagnosis.
650  0 $a Prenatal diagnosis.
650 12 $a Fetal Diseases $x ultrasonography.
650 22 $a Congenital Abnormalities $x ultrasonography.
650 22 $a Diagnosis, Differential.
650 22 $a Fetus $x abnormalities.
650 22 $a Ultrasonography, Prenatal.
856 41 $3 Table of contents only $u http://www.loc.gov/catdir/toc/ecip0710/2007005669.html
941    $a 2
952    $l I6OX771 $d 20220719010857.0
952    $l OVUX522 $d 20171226055541.0
956    $a http://locator.silo.lib.ia.us/search.cgi?index_0=id&term_0=CCAC9DAE6BF311DEA13FF332A8D7520A
994    $a 02 $b Y4Q

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