-
1
-
-
0021734131
-
Association VACTERL et hydrocephalie: Une nouvelle entite familiale
-
Briard ML, Le Merrer M, Plauchu H, Dodinval P, Lambotte C, Moraine C, Serville F (1984): Association VACTERL et hydrocephalie: Une nouvelle entite familiale. Ann Genet 27:220-223.
-
(1984)
Ann Genet
, vol.27
, pp. 220-223
-
-
Briard, M.L.1
Le Merrer, M.2
Plauchu, H.3
Dodinval, P.4
Lambotte, C.5
Moraine, C.6
Serville, F.7
-
2
-
-
0025049261
-
Prenatal ultrasonographic diagnosis of radial-ray reduction malformations
-
Brons JT, van der Harten HJ, van Geijn HP, Wiadimiroff JW, Niermeijer MF, Lindhour D, Stuart P, Meijer CJ, Arts NF (1990): Prenatal ultrasonographic diagnosis of radial-ray reduction malformations. Prenat Diagn 10:279-288.
-
(1990)
Prenat Diagn
, vol.10
, pp. 279-288
-
-
Brons, J.T.1
Van Der Harten, H.J.2
Van Geijn, H.P.3
Wiadimiroff, J.W.4
Niermeijer, M.F.5
Lindhour, D.6
Stuart, P.7
Meijer, C.J.8
Arts, N.F.9
-
3
-
-
0018361423
-
Recurrence risks for congenital hydrocephalus
-
Burton BK (1979): Recurrence risks for congenital hydrocephalus. Clin Genet 16:47-53.
-
(1979)
Clin Genet
, vol.16
, pp. 47-53
-
-
Burton, B.K.1
-
4
-
-
0000005625
-
The syndrome of sex-linked hydrocephalus
-
Edwards JH (1961): The syndrome of sex-linked hydrocephalus. Arch Dis Child 36:486-493.
-
(1961)
Arch Dis Child
, vol.36
, pp. 486-493
-
-
Edwards, J.H.1
-
6
-
-
0027490835
-
On the biologic nature of associations: Evidence from a study of radial ray deficiencies and associated malformations
-
Evans JA, Vitez M, Czeizel A (1993): On the biologic nature of associations: Evidence from a study of radial ray deficiencies and associated malformations. March of Dimes Birth Defects Foundation BD:OAS 29:63-81.
-
(1993)
March of Dimes Birth Defects Foundation BD:OAS
, vol.29
, pp. 63-81
-
-
Evans, J.A.1
Vitez, M.2
Czeizel, A.3
-
8
-
-
0003825598
-
Malformations of the VATER association plus hydrocephalus in a male infant and his maternal uncle
-
Hunter A, MacMurray B (1986): Malformations of the VATER association plus hydrocephalus in a male infant and his maternal uncle. Proc Greenwood Genet Centre 6:146-147.
-
(1986)
Proc Greenwood Genet Centre
, vol.6
, pp. 146-147
-
-
Hunter, A.1
MacMurray, B.2
-
10
-
-
0020623203
-
A population study of the VACTERL association: Evidence for its etiologic heterogeneity
-
Khoury MJ, Cordero JF, Greenberg F, Erickson JD, James LM (1983): A population study of the VACTERL association: Evidence for its etiologic heterogeneity. Pediatrics 71:815-820.
-
(1983)
Pediatrics
, vol.71
, pp. 815-820
-
-
Khoury, M.J.1
Cordero, J.F.2
Greenberg, F.3
Erickson, J.D.4
James, L.M.5
-
11
-
-
0026742503
-
VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies?
-
Porteous MEM, Cross I, Burn J (1992): VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies? Am J Med Genet 43:1032-1034.
-
(1992)
Am J Med Genet
, vol.43
, pp. 1032-1034
-
-
Porteous, M.E.M.1
Cross, I.2
Burn, J.3
-
12
-
-
2742536117
-
Multiple congenital abnormalities: Fanconi pancytopenia syndrome?
-
Sommers A, Harmel R, Zwick D (1989): Multiple congenital abnormalities: Fanconi pancytopenia syndrome? Proc Greenwood Genet Center 8: 188-190.
-
(1989)
Proc Greenwood Genet Center
, vol.8
, pp. 188-190
-
-
Sommers, A.1
Harmel, R.2
Zwick, D.3
-
13
-
-
0000635001
-
VACTERL association with hydrocephalus: A new recessive syndrome?
-
Sujansky E, Leonard B (1983): VACTERL association with hydrocephalus: A new recessive syndrome? Am J Hum Genet 35:119A.
-
(1983)
Am J Hum Genet
, vol.35
-
-
Sujansky, E.1
Leonard, B.2
-
14
-
-
0027183109
-
A duplication in the L1CAM gene associated with X-linked hydrocephalus
-
Van Camp G, Vits L, Coucke P, Lyonnet S, Schrander-Stumpel C, Darby J, Holden J, Munnich A, Willems PJ (1993): A duplication in the L1CAM gene associated with X-linked hydrocephalus. Nat Genet 4:421-425.
-
(1993)
Nat Genet
, vol.4
, pp. 421-425
-
-
Van Camp, G.1
Vits, L.2
Coucke, P.3
Lyonnet, S.4
Schrander-Stumpel, C.5
Darby, J.6
Holden, J.7
Munnich, A.8
Willems, P.J.9
-
15
-
-
0027166367
-
VACTERL with hydrocephalus: Spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance
-
Wang H, Hunter AGW, Clifford B, McLaughlin M, Thompson D (1993): VACTERL with hydrocephalus: Spontaneous chromosome breakage and rearrangement in a family showing apparent sex-linked recessive inheritance. Am J Med Genet 47:114-117.
-
(1993)
Am J Med Genet
, vol.47
, pp. 114-117
-
-
Wang, H.1
Hunter, A.G.W.2
Clifford, B.3
McLaughlin, M.4
Thompson, D.5
-
17
-
-
0025104133
-
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis
-
Willems PJ, Dijkstra I, Van der Auwera BJ, Vits L, Coucke PR, Raeymaekers P, Van Broeckheen C, Consalez GG, Freeman SB, Warren ST, Brouwer OF, Brunner HG, Renier WO, Van Elsen AF, Dumon JE (1990): Assignment of X-linked hydrocephalus to Xq28 by linkage analysis. Genomics 8:367-370.
-
(1990)
Genomics
, vol.8
, pp. 367-370
-
-
Willems, P.J.1
Dijkstra, I.2
Van Der Auwera, B.J.3
Vits, L.4
Coucke, P.R.5
Raeymaekers, P.6
Van Broeckheen, C.7
Consalez, G.G.8
Freeman, S.B.9
Warren, S.T.10
Brouwer, O.F.11
Brunner, H.G.12
Renier, W.O.13
Van Elsen, A.F.14
Dumon, J.E.15
|