-
1
-
-
0031106526
-
Three-dimensional ultrasound of the fetal spine
-
Johnson DD, Pretorius DH, Riccabona M, Budorick NE, Nelson TR. Three-dimensional ultrasound of the fetal spine. Obstet Gynecol 1997; 89:434-438.
-
(1997)
Obstet Gynecol
, vol.89
, pp. 434-438
-
-
Johnson, D.D.1
Pretorius, D.H.2
Riccabona, M.3
Budorick, N.E.4
Nelson, T.R.5
-
2
-
-
4043074926
-
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
-
4
-
-
0034105547
-
Fetal skeletal dysplasia: Three-dimensional US-initial experience
-
Garjian KV, Pretorius DH, Budorick NE, Cantrell CJ, Johnson DD, Nelson TR. Fetal skeletal dysplasia: three-dimensional US-initial experience. Radiology 2000; 214:717-723.
-
(2000)
Radiology
, vol.214
, pp. 717-723
-
-
Garjian, K.V.1
Pretorius, D.H.2
Budorick, N.E.3
Cantrell, C.J.4
Johnson, D.D.5
Nelson, T.R.6
-
5
-
-
0017900204
-
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
-
6
-
-
0032899703
-
Prenatal diagnosis of dyssegmental dysplasia: A case report
-
Hsieh YY, Chang CC, Tsai HD, Lee CC, Tsai FJ, Tsai CH. Prenatal diagnosis of dyssegmental dysplasia: a case report. J Reprod Med 1999; 44:303-305.
-
(1999)
J Reprod Med
, vol.44
, pp. 303-305
-
-
Hsieh, Y.Y.1
Chang, C.C.2
Tsai, H.D.3
Lee, C.C.4
Tsai, F.J.5
Tsai, C.H.6
-
7
-
-
4043123859
-
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
-
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
-
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
-
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
-
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
-
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
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