-
1
-
-
0036167579
-
Prenatal diagnosis of Joubert syndrome: A case report
-
Aslan H, Ulker V, Gulcan EM, et al. 2002. Prenatal diagnosis of Joubert syndrome: a case report. Prenat Diagn 22: 13-16.
-
(2002)
Prenat Diagn
, vol.22
, pp. 13-16
-
-
Aslan, H.1
Ulker, V.2
Gulcan, E.M.3
-
2
-
-
0033062767
-
Dandy-Walker malformation with postaxial polydactyly: Further evidence for autosomal recessive inheritance
-
Cavalcanti DP, Salomao MA. 1999. Dandy-Walker malformation with postaxial polydactyly: further evidence for autosomal recessive inheritance. Am J Med Genet 85: 183,184.
-
(1999)
Am J Med Genet
, vol.85
, pp. 183
-
-
Cavalcanti, D.P.1
Salomao, M.A.2
-
3
-
-
0030460388
-
Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome)
-
Chen CP, Lin SP, Liu FF, Jan SW, Lin SY, Lan CC. 1996. Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome). Am J Perinatol 13: 495-498.
-
(1996)
Am J Perinatol
, vol.13
, pp. 495-498
-
-
Chen, C.P.1
Lin, S.P.2
Liu, F.F.3
Jan, S.W.4
Lin, S.Y.5
Lan, C.C.6
-
4
-
-
0032539652
-
Grebe syndrome: Clinical and radiographic findings in affected individuals and heterozygous carriers
-
Costa T, Ramsby G, Cassia F, et al. 1998. Grebe syndrome: clinical and radiographic findings in affected individuals and heterozygous carriers. Am J Med Genet 75: 523-529.
-
(1998)
Am J Med Genet
, vol.75
, pp. 523-529
-
-
Costa, T.1
Ramsby, G.2
Cassia, F.3
-
5
-
-
0032574643
-
Neuropathologic findings in a case of OFDS type VI (Varadi syndrome)
-
Doss BJ, Jolly S, Qureshi F, et al. 1998. Neuropathologic findings in a case of OFDS type VI (Varadi syndrome). Am J Med Genet 77: 38-42.
-
(1998)
Am J Med Genet
, vol.77
, pp. 38-42
-
-
Doss, B.J.1
Jolly, S.2
Qureshi, F.3
-
6
-
-
0023730380
-
Comparative histopathology of the growth cartilage in short-rib polydactyly syndromes type I and type III and in chondroectodermal dysplasia
-
Erzen M, Stanescu R, Stanescu V, Maroteaux P. 1988. Comparative histopathology of the growth cartilage in short-rib polydactyly syndromes type I and type III and in chondroectodermal dysplasia. Ann Genet 31: 144-150.
-
(1988)
Ann Genet
, vol.31
, pp. 144-150
-
-
Erzen, M.1
Stanescu, R.2
Stanescu, V.3
Maroteaux, P.4
-
7
-
-
0034982483
-
Mesomelic camptomelia, polydactyly and Dandy-Walker cyst in siblings
-
Guschmann M, Horn D, Entezami M, et al. 2001. Mesomelic camptomelia, polydactyly and Dandy-Walker cyst in siblings. Prenat Diagn 21: 378-382.
-
(2001)
Prenat Diagn
, vol.21
, pp. 378-382
-
-
Guschmann, M.1
Horn, D.2
Entezami, M.3
-
8
-
-
0031758193
-
Transvaginal sonographic diagnosis of shortrib polydactyly dysplasia at 13 weeks' gestation
-
Hill LM, Leary J. 1998. Transvaginal sonographic diagnosis of shortrib polydactyly dysplasia at 13 weeks' gestation. Prenat Diagn 18: 1198-1201.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1198-1201
-
-
Hill, L.M.1
Leary, J.2
-
9
-
-
0032859020
-
Prenatal diagnosis of thoracopelvic dysplasia. A case report
-
Hsieh YY, Hsu TY, Lee CC, Chang CC, Tsai HD, Tsai CH. 1999. Prenatal diagnosis of thoracopelvic dysplasia. A case report. J Reprod Med 44: 737-740.
-
(1999)
J Reprod Med
, vol.44
, pp. 737-740
-
-
Hsieh, Y.Y.1
Hsu, T.Y.2
Lee, C.C.3
Chang, C.C.4
Tsai, H.D.5
Tsai, C.H.6
-
10
-
-
0024401414
-
Dandy-Walker malformation with postaxial polydactyly: A new syndrome?
-
Pierquin G, Deroover J, Levi S, Masson T, Hayez-Delatte F, Van Regemorter N. 1989. Dandy-Walker malformation with postaxial polydactyly: a new syndrome? Am J Med Genet 33: 483,484.
-
(1989)
Am J Med Genet
, vol.33
, pp. 483
-
-
Pierquin, G.1
Deroover, J.2
Levi, S.3
Masson, T.4
Hayez-Delatte, F.5
Van Regemorter, N.6
-
11
-
-
0028950058
-
Dandy-Walker malformation in the Meckel syndrome
-
Summers MC, Donnenfeld AE. 1995. Dandy-Walker malformation in the Meckel syndrome. Am J Med Genet 55: 57-61.
-
(1995)
Am J Med Genet
, vol.55
, pp. 57-61
-
-
Summers, M.C.1
Donnenfeld, A.E.2
-
12
-
-
0026598703
-
Acromelic frontonasal "dysplasia": Further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome)
-
Verloes A, Gillerot Y, Walczak E, Van Maldergem L, Koulischer L. 1992. Acromelic frontonasal "dysplasia": further delineation of a subtype with brain malformation and polydactyly (Toriello syndrome). Am J Med Genet 42: 180-183.
-
(1992)
Am J Med Genet
, vol.42
, pp. 180-183
-
-
Verloes, A.1
Gillerot, Y.2
Walczak, E.3
Van Maldergem, L.4
Koulischer, L.5
|