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Volumn 25, Issue 4, 2006, Pages 539-543

Prenatal diagnosis of spondylocostal dysostosis with 3-dimensional ultrasonography

Author keywords

[No Author keywords available]

Indexed keywords

BIOMEDICAL ENGINEERING; DIAGNOSIS; IMAGE SEGMENTATION; PATIENT MONITORING;

EID: 33646050010     PISSN: 02784297     EISSN: None     Source Type: Journal    
DOI: 10.7863/jum.2006.25.4.539     Document Type: Article
Times cited : (6)

References (13)
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    • Prenatal diagnosis of fetal skeletal dysplasias by combining two-dimensional and three-dimensional ultrasound and intrauterine three-dimensional helical computer tomography
    • Ruano R, Molho M, Roume J, Ville Y. Prenatal diagnosis of fetal skeletal dysplasias by combining two-dimensional and three-dimensional ultrasound and intrauterine three-dimensional helical computer tomography. Ultrasound Obstet Gynecol 2004; 24:134-140.
    • (2004) Ultrasound Obstet Gynecol , vol.24 , pp. 134-140
    • Ruano, R.1    Molho, M.2    Roume, J.3    Ville, Y.4
  • 3
    • 0034477396 scopus 로고    scopus 로고
    • Three-dimensional ultrasound in the evaluation of fetal anomalies
    • Dyson RL, Pretorius DH, Budorick NE, et al. Three-dimensional ultrasound in the evaluation of fetal anomalies. Ultrasound Obstet Gynecol 2000; 16:321-328.
    • (2000) Ultrasound Obstet Gynecol , vol.16 , pp. 321-328
    • Dyson, R.L.1    Pretorius, D.H.2    Budorick, N.E.3
  • 5
    • 0017900204 scopus 로고
    • Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): A new genetic entity?
    • Wadia RS, Shirole DB, Dikshit MS. Recessively inherited costovertebral segmentation defect with mesomelia and peculiar facies (Covesdem syndrome): a new genetic entity? J Med Genet 1978; 15:123-127.
    • (1978) J Med Genet , vol.15 , pp. 123-127
    • Wadia, R.S.1    Shirole, D.B.2    Dikshit, M.S.3
  • 7
    • 4043123859 scopus 로고    scopus 로고
    • Prenatal diagnosis of hemifacial microsomia and ipsilateral cerebellar hypoplasia in a fetus with oculoauriculovertebral spectrum
    • Martinelli P, Maruotti GM, Agangi A, Mazzarelli LL, Bifulco G, Paladini D. Prenatal diagnosis of hemifacial microsomia and ipsilateral cerebellar hypoplasia in a fetus with oculoauriculovertebral spectrum. Ultrasound Obstet Gynecol 2004; 24:199-201.
    • (2004) Ultrasound Obstet Gynecol , vol.24 , pp. 199-201
    • Martinelli, P.1    Maruotti, G.M.2    Agangi, A.3    Mazzarelli, L.L.4    Bifulco, G.5    Paladini, D.6
  • 8
    • 0032920311 scopus 로고    scopus 로고
    • VACTERL manifestations in two generations of a family
    • Nezarati MM, McLeod DR. VACTERL manifestations in two generations of a family. Am J Med Genet 1999; 82:40-42.
    • (1999) Am J Med Genet , vol.82 , pp. 40-42
    • Nezarati, M.M.1    McLeod, D.R.2
  • 9
    • 0001741191 scopus 로고
    • Hereditary malformations of the vertebral bodies
    • Jarcho S, Levin PM. Hereditary malformations of the vertebral bodies. Johns Hopkins Med J 1938; 62:216-226.
    • (1938) Johns Hopkins Med J , vol.62 , pp. 216-226
    • Jarcho, S.1    Levin, P.M.2
  • 10
    • 0013985215 scopus 로고
    • A syndrome of bizarre vertebral anomalies
    • Lavy NW, Palmer CG, Merritt AD. A syndrome of bizarre vertebral anomalies. J Pediat 1966; 69:1121-1125.
    • (1966) J Pediat , vol.69 , pp. 1121-1125
    • Lavy, N.W.1    Palmer, C.G.2    Merritt, A.D.3
  • 12
    • 0022471829 scopus 로고
    • Spondylocostal/spondylothoracic dysostosis: The clinical basis for prognosticating and genetic counseling
    • Ayme S, Preus M. Spondylocostal/spondylothoracic dysostosis: the clinical basis for prognosticating and genetic counseling. Am J Med Genet 1986; 24:599-606.
    • (1986) Am J Med Genet , vol.24 , pp. 599-606
    • Ayme, S.1    Preus, M.2
  • 13
    • 0030064549 scopus 로고    scopus 로고
    • Multiple vertebral segmentation defects: Analysis of 26 new patients and review of the literature
    • Mortier GR, Lachman RS, Bocian M, Rimoin DL. Multiple vertebral segmentation defects: analysis of 26 new patients and review of the literature. Am J Med Genet 1996; 61:310-319
    • (1996) Am J Med Genet , vol.61 , pp. 310-319
    • Mortier, G.R.1    Lachman, R.S.2    Bocian, M.3    Rimoin, D.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.