-
1
-
-
0033781778
-
The contribution of the adriamycin-induced rat model of the VATER association to our understanding of congenital abnormalities and their embryogenesis
-
Beasley SW, Diez Pardo J, Qi BQ, Tovar JA, Xia HM. 2000. The contribution of the adriamycin-induced rat model of the VATER association to our understanding of congenital abnormalities and their embryogenesis. Pediatr Surg Int 16:465-472.
-
(2000)
Pediatr Surg Int
, vol.16
, pp. 465-472
-
-
Beasley, S.W.1
Diez Pardo, J.2
Qi, B.Q.3
Tovar, J.A.4
Xia, H.M.5
-
2
-
-
0030911255
-
The spectrum of congenital anomalies of the VATER association: An international study
-
Botto LD, Khoury MJ, Mastroiacovo P, Castilla EE, MooreCA, Skjaerven R, Mutchinick OM, Borman B, Cocchi G, Czeizel AE, Goujard J, Irgens LM, Lancaster PAL, Martínez-Frías ML, Merlob P, Ruusinen A, Stoll C, Sumiyoshi Y. 1997. The spectrum of congenital anomalies of the VATER association: An international study. Am J Med Genet 71:8-15.
-
(1997)
Am J Med Genet
, vol.71
, pp. 8-15
-
-
Botto, L.D.1
Khoury, M.J.2
Mastroiacovo, P.3
Castilla, E.E.4
Moore, C.A.5
Skjaerven, R.6
Mutchinick, O.M.7
Borman, B.8
Cocchi, G.9
Czeizel, A.E.10
Goujard, J.11
Irgens, L.M.12
Lancaster, P.A.L.13
Martínez-Frías, M.L.14
Merlob, P.15
Ruusinen, A.16
Stoll, C.17
Sumiyoshi, Y.18
-
4
-
-
0022374474
-
An aetiological study of the VACTERL association
-
Czeizel A, Ludányi I. 1985. An aetiological study of the VACTERL association. Eur J Pediatr 144:331-337.
-
(1985)
Eur J Pediatr
, vol.144
, pp. 331-337
-
-
Czeizel, A.1
Ludányi, I.2
-
5
-
-
34848858478
-
Adriamycin produces a reproducible teratogenic model of vertebral, anal, cardiovascular, tracheal, esophageal, renal, and limb anomalies in the mouse
-
Dawrant MJ, Giles S, Bannigan J, Puri P. 2007. Adriamycin produces a reproducible teratogenic model of vertebral, anal, cardiovascular, tracheal, esophageal, renal, and limb anomalies in the mouse. J Pediatr Surg 42:1652-1658.
-
(2007)
J Pediatr Surg
, vol.42
, pp. 1652-1658
-
-
Dawrant, M.J.1
Giles, S.2
Bannigan, J.3
Puri, P.4
-
6
-
-
23344449113
-
Should chromosome breakage studies be performed in patients with VACTERL association?
-
Faivre L, Portnoï MF, Pals G, Stoppa-Lyonnet D, Le Merrer M, Thauvin-Robinet C, Huet F, Mathew CG, Joenje H, Verloes A, Baumann C. 2005. Should chromosome breakage studies be performed in patients with VACTERL association? Am J Med Genet Part A 137A:55-58.
-
(2005)
Am J Med Genet
, vol.137 A
, Issue.PART A
, pp. 55-58
-
-
Faivre, L.1
Portnoï, M.F.2
Pals, G.3
Stoppa-Lyonnet, D.4
Le Merrer, M.5
Thauvin-Robinet, C.6
Huet, F.7
Mathew, C.G.8
Joenje, H.9
Verloes, A.10
Baumann, C.11
-
8
-
-
33846420646
-
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1β in persistent cloaca and associated kidney malformations
-
Jenkins D, Bitner-Glindzicz M, Thomasson L, Malcolm S, Warne SA, Feather SA, Flanagan SE, Ellard S, Bingham C, Santos L, Henkemeyer M, Zinn A, Baker LA, Duncan T, Wilcox DT, Woolf AS. 2007. Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1β in persistent cloaca and associated kidney malformations. J Pediatr Urol 3:2-9.
-
(2007)
J Pediatr Urol
, vol.3
, pp. 2-9
-
-
Jenkins, D.1
Bitner-Glindzicz, M.2
Thomasson, L.3
Malcolm, S.4
Warne, S.A.5
Feather, S.A.6
Flanagan, S.E.7
Ellard, S.8
Bingham, C.9
Santos, L.10
Henkemeyer, M.11
Zinn, A.12
Baker, L.A.13
Duncan, T.14
Wilcox, D.T.15
Woolf, A.S.16
-
9
-
-
0342936349
-
VATER non-random association of congenital malformations: Study based on data from four malformation registers
-
Källén K, Mastroiacovo P, Castilla EE, Robert E, Källén B. 2001. VATER non-random association of congenital malformations: Study based on data from four malformation registers. Am J Med Genet 10:26-32.
-
(2001)
Am J Med Genet
, vol.10
, pp. 26-32
-
-
Källén, K.1
Mastroiacovo, P.2
Castilla, E.E.3
Robert, E.4
Källén, B.5
-
10
-
-
33947523679
-
VACTERL anomalies in patients with esophageal atresia: An updated delineation of the spectrum and review of the literature
-
Keckler SJ, St Peter SD, Valusek PA, Tsao K, Snyder CL, Holcomb GW III, Ostlie DJ. 2007. VACTERL anomalies in patients with esophageal atresia: An updated delineation of the spectrum and review of the literature. Pediatr Surg Int 23:309-313.
-
(2007)
Pediatr Surg Int
, vol.23
, pp. 309-313
-
-
Keckler, S.J.1
St Peter, S.D.2
Valusek, P.A.3
Tsao, K.4
Snyder, C.L.5
Holcomb III, G.W.6
Ostlie, D.J.7
-
11
-
-
0020623203
-
A population study of the VACTERL association: Evidence for its etiologic heterogeneity
-
Khoury MJ, Cordero JF, Greenberg F, James LM, Erickson JD. 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
James, L.M.4
Erickson, J.D.5
-
12
-
-
0035141226
-
Murine models of VACTERL syndrome: Role of sonic hedgehog signaling pathway
-
Kim PC, Mo R, Hui Cc C. 2001. Murine models of VACTERL syndrome: Role of sonic hedgehog signaling pathway. J Pediatr Surg 36:381-384.
-
(2001)
J Pediatr Surg
, vol.36
, pp. 381-384
-
-
Kim, P.C.1
Mo, R.2
Hui, C.C.3
-
13
-
-
34648813016
-
A female infant who had both complete VACTERL association and MURCS association: Report of a case
-
Komura M, Kanamori Y, Sugiyama M, Tomonaga T, Suzuki K, Hashizume K, Goishi K. 2007. A female infant who had both complete VACTERL association and MURCS association: Report of a case. Surg Today 37: 878-880.
-
(2007)
Surg Today
, vol.37
, pp. 878-880
-
-
Komura, M.1
Kanamori, Y.2
Sugiyama, M.3
Tomonaga, T.4
Suzuki, K.5
Hashizume, K.6
Goishi, K.7
-
14
-
-
33845192028
-
Sonic hedgehog, BMP4, and Hox genes in the development of anorectal malformations in ethylenethiourea-exposed fetal rats
-
Mandhan P, Quan QB, Beasley S, Sullivan M. 2006. Sonic hedgehog, BMP4, and Hox genes in the development of anorectal malformations in ethylenethiourea-exposed fetal rats. J Pediatr Surg 41:2041-2045.
-
(2006)
J Pediatr Surg
, vol.41
, pp. 2041-2045
-
-
Mandhan, P.1
Quan, Q.B.2
Beasley, S.3
Sullivan, M.4
-
15
-
-
0345320262
-
VACTERL as primary, polytopic developmental field defects
-
Martínez-Frías ML, Frías JL. 1999. VACTERL as primary, polytopic developmental field defects. Am J Med Genet 83:13-16.
-
(1999)
Am J Med Genet
, vol.83
, pp. 13-16
-
-
Martínez-Frías, M.L.1
Frías, J.L.2
-
16
-
-
33846040372
-
A 1.5-Mb-resolution radiation hybrid map of the cat genome and comparative analysis with the canine and human genomes
-
Murphy WJ, Davis B, David VA, Agarwala R, Schäffer AA, Pearks Wilkerson AJ, Neelam B, O'Brien SJ, Menotti-Raymond M. 2007. A 1.5-Mb-resolution radiation hybrid map of the cat genome and comparative analysis with the canine and human genomes. Genomics 89:189-196.
-
(2007)
Genomics
, vol.89
, pp. 189-196
-
-
Murphy, W.J.1
Davis, B.2
David, V.A.3
Agarwala, R.4
Schäffer, A.A.5
Pearks Wilkerson, A.J.6
Neelam, B.7
O'Brien, S.J.8
Menotti-Raymond, M.9
-
17
-
-
38149074665
-
Congenital abnormalities of the feline vertebral column
-
Newitt A, German AJ, Barr FJ. 2008. Congenital abnormalities of the feline vertebral column. Vet Radiol Ultrasound 49:35-41.
-
(2008)
Vet Radiol Ultrasound
, vol.49
, pp. 35-41
-
-
Newitt, A.1
German, A.J.2
Barr, F.J.3
-
18
-
-
0030002181
-
VACTERL association, epidemiologic definition and delineation
-
Rittler M, Paz JE, Castilla EE. 1996. VACTERL association, epidemiologic definition and delineation. Am J Med Genet 63:529-536.
-
(1996)
Am J Med Genet
, vol.63
, pp. 529-536
-
-
Rittler, M.1
Paz, J.E.2
Castilla, E.E.3
-
20
-
-
44849135766
-
VACTERL/ caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5
-
Szumska D, Pieles G, Essalmani R, Bilski M, Mesnard D, Kaur K, Franklyn A, El Omari K, Jefferis J, Bentham J, Taylor JM, Schneider JE, Arnold SJ, Johnson P, Tymowska-Lalanne Z, Stammers D, Clarke K, Neubauer S, Morris A, Brown SD, Shaw-Smith C, Cama A, Capra V, Ragoussis J, Constam D, Seidah NG, Prat A, Bhattacharya S. 2008. VACTERL/ caudal regression/Currarino syndrome-like malformations in mice with mutation in the proprotein convertase Pcsk5. Genes Dev 22:1465-1477.
-
(2008)
Genes Dev
, vol.22
, pp. 1465-1477
-
-
Szumska, D.1
Pieles, G.2
Essalmani, R.3
Bilski, M.4
Mesnard, D.5
Kaur, K.6
Franklyn, A.7
El Omari, K.8
Jefferis, J.9
Bentham, J.10
Taylor, J.M.11
Schneider, J.E.12
Arnold, S.J.13
Johnson, P.14
Tymowska-Lalanne, Z.15
Stammers, D.16
Clarke, K.17
Neubauer, S.18
Morris, A.19
Brown, S.D.20
Shaw-Smith, C.21
Cama, A.22
Capra, V.23
Ragoussis, J.24
Constam, D.25
Seidah, N.G.26
Prat, A.27
Bhattacharya, S.28
more..
-
21
-
-
0014676766
-
Subvalvular pulmonary stenosis and aorticopulmonary septal defect in the cat
-
Will JA. 1969. Subvalvular pulmonary stenosis and aorticopulmonary septal defect in the cat. J Am Vet Med Assoc 154:913-916.
-
(1969)
J Am Vet Med Assoc
, vol.154
, pp. 913-916
-
-
Will, J.A.1
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