-
1
-
-
77954287928
-
Prevalence of dental anomalies in a population of cleft lip and palate patients
-
Al Jamal GA, Hazza'a AM, Rawashdeh MA,. 2010. Prevalence of dental anomalies in a population of cleft lip and palate patients. Cleft Palate Craniofac J. 47 (4): 413-420.
-
(2010)
Cleft Palate Craniofac J
, vol.47
, Issue.4
, pp. 413-420
-
-
Al Jamal, G.A.1
Hazza'A, A.M.2
Rawashdeh, M.A.3
-
2
-
-
84902084105
-
Expanding the cleft phenotype: The dental characteristics of unaffected parents of Australian children with non-syndromic cleft lip and palate
-
Aspinall A, Raj S, Jugessur A, Marazita M, Savarirayan R, Kilpatrick N., 2014. Expanding the cleft phenotype: the dental characteristics of unaffected parents of Australian children with non-syndromic cleft lip and palate. Int J Paediatr Dent. 24 (4): 286-292.
-
(2014)
Int J Paediatr Dent
, vol.24
, Issue.4
, pp. 286-292
-
-
Aspinall, A.1
Raj, S.2
Jugessur, A.3
Marazita, M.4
Savarirayan, R.5
Kilpatrick, N.6
-
3
-
-
84903311286
-
Dental enamel development: Proteinases and their enamel matrix substrates
-
Bartlett JD,. 2013. Dental enamel development: proteinases and their enamel matrix substrates. ISRN Dent. 2013: 684607.
-
(2013)
ISRN Dent
, vol.2013
, pp. 684607
-
-
Bartlett, J.D.1
-
4
-
-
84904284419
-
Kallikrein-related peptidase-4 (KLK4): Role in enamel formation and revelations from ablated mice
-
Bartlett JD, Simmer JP,. 2014. Kallikrein-related peptidase-4 (KLK4): role in enamel formation and revelations from ablated mice. Front Physiol. 5: 240.
-
(2014)
Front Physiol
, vol.5
, pp. 240
-
-
Bartlett, J.D.1
Simmer, J.P.2
-
5
-
-
84903793174
-
Interferon regulatory factor 6 regulates keratinocyte migration
-
Biggs LC, Naridze RL, DeMali KA, Lusche DF, Kuhl S, Soll DR, Schutte BC, Dunnwald M., 2014. Interferon regulatory factor 6 regulates keratinocyte migration. J Cell Sci. 127 (Pt 13): 2840-2848.
-
(2014)
J Cell Sci
, vol.127
, pp. 2840-2848
-
-
Biggs, L.C.1
Naridze, R.L.2
DeMali, K.A.3
Lusche, D.F.4
Kuhl, S.5
Soll, D.R.6
Schutte, B.C.7
Dunnwald, M.8
-
6
-
-
84856083695
-
Interferon regulatory factor 6 is necessary, but not sufficient, for keratinocyte differentiation
-
Biggs LC, Rhea L, Schutte BC, Dunnwald M., 2012. Interferon regulatory factor 6 is necessary, but not sufficient, for keratinocyte differentiation. J Invest Dermatol. 132 (1): 50-58.
-
(2012)
J Invest Dermatol
, vol.132
, Issue.1
, pp. 50-58
-
-
Biggs, L.C.1
Rhea, L.2
Schutte, B.C.3
Dunnwald, M.4
-
7
-
-
84862788362
-
The role of Irf6 in tooth epithelial invagination
-
Blackburn J, Ohazama A, Kawasaki K, Otsuka-Tanaka Y, Liu B, Honda K, Rountree RB, Hu Y, Kawasaki M, Birchmeier W, et al. 2012. The role of Irf6 in tooth epithelial invagination. Dev Biol. 365 (1): 61-70.
-
(2012)
Dev Biol
, vol.365
, Issue.1
, pp. 61-70
-
-
Blackburn, J.1
Ohazama, A.2
Kawasaki, K.3
Otsuka-Tanaka, Y.4
Liu, B.5
Honda, K.6
Rountree, R.B.7
Hu, Y.8
Kawasaki, M.9
Birchmeier, W.10
-
8
-
-
79951800135
-
Cleft lip and palate: Understanding genetic and environmental influences
-
Dixon MJ, Marazita ML, Beaty TH, Murray JC,. 2011. Cleft lip and palate: understanding genetic and environmental influences. Nat Rev Genet. 12 (3): 167-178.
-
(2011)
Nat Rev Genet
, vol.12
, Issue.3
, pp. 167-178
-
-
Dixon, M.J.1
Marazita, M.L.2
Beaty, T.H.3
Murray, J.C.4
-
9
-
-
0034945729
-
Hypodontia and tooth formation in groups of children with cleft, siblings without cleft, and nonrelated controls
-
Eerens K, Vlietinck R, Heidbuchel K, Van Olmen A, Derom C, Willems G, Carels C., 2001. Hypodontia and tooth formation in groups of children with cleft, siblings without cleft, and nonrelated controls. Cleft Palate Craniofac J. 38 (4): 374-378.
-
(2001)
Cleft Palate Craniofac J
, vol.38
, Issue.4
, pp. 374-378
-
-
Eerens, K.1
Vlietinck, R.2
Heidbuchel, K.3
Van Olmen, A.4
Derom, C.5
Willems, G.6
Carels, C.7
-
10
-
-
80054744189
-
A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis
-
Ferretti E, Li B, Zewdu R, Wells V, Hebert JM, Karner C, Anderson MJ, Williams T, Dixon J, Dixon MJ, et al. 2011. A conserved Pbx-Wnt-p63-Irf6 regulatory module controls face morphogenesis by promoting epithelial apoptosis. Developmental Cell. 21 (4): 627-641.
-
(2011)
Developmental Cell
, vol.21
, Issue.4
, pp. 627-641
-
-
Ferretti, E.1
Li, B.2
Zewdu, R.3
Wells, V.4
Hebert, J.M.5
Karner, C.6
Anderson, M.J.7
Williams, T.8
Dixon, J.9
Dixon, M.J.10
-
11
-
-
84872424112
-
Deficiency in acellular cementum and periodontal attachment in bsp null mice
-
Foster BL, Soenjaya Y, Nociti FH Jr, Holm E, Zerfas PM, Wimer HF, Holdsworth DW, Aubin JE, Hunter GK, Goldberg HA, et al. 2013. Deficiency in acellular cementum and periodontal attachment in bsp null mice. J Dent Res. 92 (2): 166-172.
-
(2013)
J Dent Res
, vol.92
, Issue.2
, pp. 166-172
-
-
Foster, B.L.1
Soenjaya, Y.2
Nociti, F.H.J.3
Holm, E.4
Zerfas, P.M.5
Wimer, H.F.6
Holdsworth, D.W.7
Aubin, J.E.8
Hunter, G.K.9
Goldberg, H.A.10
-
12
-
-
67650129719
-
Enamel defects in maxillary central incisors of infants with unilateral cleft lip
-
Gomes AC, Neves LT, Gomide MR,. 2009. Enamel defects in maxillary central incisors of infants with unilateral cleft lip. Cleft Palate Craniofac J. 46 (4): 420-424.
-
(2009)
Cleft Palate Craniofac J
, vol.46
, Issue.4
, pp. 420-424
-
-
Gomes, A.C.1
Neves, L.T.2
Gomide, M.R.3
-
13
-
-
84862918759
-
Epithelial-specific knockout of the Rac1 gene leads to enamel defects. Eur J Oral Sci
-
Huang Z, Kim J, Lacruz RS, Bringas P Jr, Glogauer M, Bromage TG, Kaartinen VM, Snead ML,. 2011. Epithelial-specific knockout of the Rac1 gene leads to enamel defects. Eur J Oral Sci. 119 Suppl 1: 168-176.
-
(2011)
119 Suppl
, vol.1
, pp. 168-176
-
-
Huang, Z.1
Kim, J.2
Lacruz, R.S.3
Bringas, P.J.4
Glogauer, M.5
Bromage, T.G.6
Kaartinen, V.M.7
Snead, M.L.8
-
14
-
-
33750452339
-
Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)
-
Ingraham CR, Kinoshita A, Kondo S, Yang B, Sajan S, Trout KJ, Malik MI, Dunnwald M, Goudy SL, Lovett M, et al. 2006. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6). Nat Genet. 38 (11): 1335-1340.
-
(2006)
Nat Genet
, vol.38
, Issue.11
, pp. 1335-1340
-
-
Ingraham, C.R.1
Kinoshita, A.2
Kondo, S.3
Yang, B.4
Sajan, S.5
Trout, K.J.6
Malik, M.I.7
Dunnwald, M.8
Goudy, S.L.9
Lovett, M.10
-
15
-
-
33744922620
-
Developmental expression analysis of the mouse and chick orthologues of IRF6: The gene mutated in Van der Woude syndrome
-
Knight AS, Schutte BC, Jiang R, Dixon MJ,. 2006. Developmental expression analysis of the mouse and chick orthologues of IRF6: the gene mutated in Van der Woude syndrome. Dev Dyn. 235 (5): 1441-1447.
-
(2006)
Dev Dyn
, vol.235
, Issue.5
, pp. 1441-1447
-
-
Knight, A.S.1
Schutte, B.C.2
Jiang, R.3
Dixon, M.J.4
-
16
-
-
18644374446
-
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes
-
Kondo S, Schutte BC, Richardson RJ, Bjork BC, Knight AS, Watanabe Y, Howard E, de Lima RL, Daack-Hirsch S, Sander A, et al. 2002. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes. Nat Genet. 32 (2): 285-289.
-
(2002)
Nat Genet
, vol.32
, Issue.2
, pp. 285-289
-
-
Kondo, S.1
Schutte, B.C.2
Richardson, R.J.3
Bjork, B.C.4
Knight, A.S.5
Watanabe, Y.6
Howard, E.7
De Lima, R.L.8
Daack-Hirsch, S.9
Sander, A.10
-
17
-
-
84902678923
-
Regulatory mechanisms of Hertwigs epithelial root sheath formation and anomaly correlated with root length
-
Kumakami-Sakano M, Otsu K, Fujiwara N, Harada H., 2014. Regulatory mechanisms of Hertwigs epithelial root sheath formation and anomaly correlated with root length. Exp Cell Res. 325 (2): 78-82.
-
(2014)
Exp Cell Res
, vol.325
, Issue.2
, pp. 78-82
-
-
Kumakami-Sakano, M.1
Otsu, K.2
Fujiwara, N.3
Harada, H.4
-
18
-
-
84890369688
-
A model for the molecular underpinnings of tooth defects in Axenfeld-Rieger syndrome
-
Li X, Venugopalan SR, Cao H, Pinho FO, Paine ML, Snead ML, Semina EV, Amendt BA,. 2014. A model for the molecular underpinnings of tooth defects in Axenfeld-Rieger syndrome. Hum Mol Genet. 23 (1): 194-208.
-
(2014)
Hum Mol Genet
, vol.23
, Issue.1
, pp. 194-208
-
-
Li, X.1
Venugopalan, S.R.2
Cao, H.3
Pinho, F.O.4
Paine, M.L.5
Snead, M.L.6
Semina, E.V.7
Amendt, B.A.8
-
19
-
-
84872583041
-
-
In: Proceedings of SPIE 8506: developments in x-ray tomography VIII, 85060X, San Diego, CA
-
Limaye A,. 2012. Drishti: a volume exploration and presentation tool. In: Proceedings of SPIE 8506: developments in x-ray tomography VIII, 85060X, San Diego, CA.
-
(2012)
Drishti: A Volume Exploration and Presentation Tool
-
-
Limaye, A.1
-
20
-
-
37349092090
-
Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis
-
Liu F, Chu EY, Watt B, Zhang Y, Gallant NM, Andl T, Yang SH, Lu MM, Piccolo S, Schmidt-Ullrich R, et al. 2008. Wnt/beta-catenin signaling directs multiple stages of tooth morphogenesis. Dev Biol. 313 (1): 210-224.
-
(2008)
Dev Biol
, vol.313
, Issue.1
, pp. 210-224
-
-
Liu, F.1
Chu, E.Y.2
Watt, B.3
Zhang, Y.4
Gallant, N.M.5
Andl, T.6
Yang, S.H.7
Lu, M.M.8
Piccolo, S.9
Schmidt-Ullrich, R.10
-
21
-
-
0346888506
-
Genetic dissection of Pitx2 in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration
-
Liu W, Selever J, Lu MF, Martin JF,. 2003. Genetic dissection of Pitx2 in craniofacial development uncovers new functions in branchial arch morphogenesis, late aspects of tooth morphogenesis and cell migration. Development. 130 (25): 6375-6385.
-
(2003)
Development
, vol.130
, Issue.25
, pp. 6375-6385
-
-
Liu, W.1
Selever, J.2
Lu, M.F.3
Martin, J.F.4
-
22
-
-
51149111177
-
Taurodontism and Van der Woude syndrome: Is there an association?
-
Nawa H, Oberoi S, Vargervik K., 2008. Taurodontism and Van der Woude syndrome: is there an association? Angle Orthod. 78 (5): 832-837.
-
(2008)
Angle Orthod
, vol.78
, Issue.5
, pp. 832-837
-
-
Nawa, H.1
Oberoi, S.2
Vargervik, K.3
-
23
-
-
0025646473
-
Localization of adherens junction proteins along the possible sliding interface between secretory ameloblasts of the rat incisor
-
Nishikawa S, Tsukita S, Tsukita S, Sasa S., 1990. Localization of adherens junction proteins along the possible sliding interface between secretory ameloblasts of the rat incisor. Cell Struct Funct. 15 (5): 245-249.
-
(1990)
Cell Struct Funct
, vol.15
, Issue.5
, pp. 245-249
-
-
Nishikawa, S.1
Tsukita, S.2
Tsukita, S.3
Sasa, S.4
-
24
-
-
25144441034
-
Hypoplasia and hypodontia in Van der Woude syndrome
-
Oberoi S, Vargervik K., 2005. Hypoplasia and hypodontia in Van der Woude syndrome. Cleft Palate Craniofac J. 42 (5): 459-466.
-
(2005)
Cleft Palate Craniofac J
, vol.42
, Issue.5
, pp. 459-466
-
-
Oberoi, S.1
Vargervik, K.2
-
25
-
-
0035836637
-
Tumor metastasis suppressor nm23H1 regulates Rac1 GTPase by interaction with Tiam1
-
Otsuki Y, Tanaka M, Yoshii S, Kawazoe N, Nakaya K, Sugimura H., 2001. Tumor metastasis suppressor nm23H1 regulates Rac1 GTPase by interaction with Tiam1. Proc Natl Acad Sci U S A. 98 (8): 4385-4390.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, Issue.8
, pp. 4385-4390
-
-
Otsuki, Y.1
Tanaka, M.2
Yoshii, S.3
Kawazoe, N.4
Nakaya, K.5
Sugimura, H.6
-
26
-
-
41849085173
-
Familial non-syndromic cleft lip and palate: Analysis of the IRF6 gene and clinical phenotypes
-
Pegelow M, Peyrard-Janvid M, Zucchelli M, Fransson I, Larson O, Kere J, Larsson C, Karsten A., 2008. Familial non-syndromic cleft lip and palate: analysis of the IRF6 gene and clinical phenotypes. Eur J Orthod. 30 (2): 169-175.
-
(2008)
Eur J Orthod
, vol.30
, Issue.2
, pp. 169-175
-
-
Pegelow, M.1
Peyrard-Janvid, M.2
Zucchelli, M.3
Fransson, I.4
Larson, O.5
Kere, J.6
Larsson, C.7
Karsten, A.8
-
27
-
-
84891832380
-
Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development
-
Peyrard-Janvid M, Leslie EJ, Kousa YA, Smith TL, Dunnwald M, Magnusson M, Lentz BA, Unneberg P, Fransson I, Koillinen HK, et al. 2014. Dominant mutations in GRHL3 cause Van der Woude Syndrome and disrupt oral periderm development. Am J Hum Genet. 94 (1): 23-32.
-
(2014)
Am J Hum Genet
, vol.94
, Issue.1
, pp. 23-32
-
-
Peyrard-Janvid, M.1
Leslie, E.J.2
Kousa, Y.A.3
Smith, T.L.4
Dunnwald, M.5
Magnusson, M.6
Lentz, B.A.7
Unneberg, P.8
Fransson, I.9
Koillinen, H.K.10
-
28
-
-
0022745244
-
A review of tooth formation in children with cleft lip/palate
-
Ranta R,. 1986. A review of tooth formation in children with cleft lip/palate. Am J Orthod Dentofacial Orthop. 90 (1): 11-18.
-
(1986)
Am J Orthod Dentofacial Orthop
, vol.90
, Issue.1
, pp. 11-18
-
-
Ranta, R.1
-
29
-
-
0020452269
-
Tooth anomalies associated with congenital sinuses of the lower lip and cleft lip/palate
-
Ranta R, Rintala A., 1982. Tooth anomalies associated with congenital sinuses of the lower lip and cleft lip/palate. Angle Orthod. 52 (3): 212-221.
-
(1982)
Angle Orthod
, vol.52
, Issue.3
, pp. 212-221
-
-
Ranta, R.1
Rintala, A.2
-
30
-
-
33750441851
-
Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch
-
Richardson RJ, Dixon J, Malhotra S, Hardman MJ, Knowles L, Boot-Handford RP, Shore P, Whitmarsh A, Dixon MJ,. 2006. Irf6 is a key determinant of the keratinocyte proliferation-differentiation switch. Nat Genet. 38 (11): 1329-1334.
-
(2006)
Nat Genet
, vol.38
, Issue.11
, pp. 1329-1334
-
-
Richardson, R.J.1
Dixon, J.2
Malhotra, S.3
Hardman, M.J.4
Knowles, L.5
Boot-Handford, R.P.6
Shore, P.7
Whitmarsh, A.8
Dixon, M.J.9
-
31
-
-
84946110836
-
Prevalence of dental anomalies in children with cleft lip and unilateral and bilateral cleft lip and palate
-
Rullo R, Festa VM, Rullo R, Addabbo F, Chiodini P, Vitale M, Perillo L., 2015. Prevalence of dental anomalies in children with cleft lip and unilateral and bilateral cleft lip and palate. Eur J Paediatr Dent. 16 (3): 229-232.
-
(2015)
Eur J Paediatr Dent
, vol.16
, Issue.3
, pp. 229-232
-
-
Rullo, R.1
Festa, V.M.2
Rullo, R.3
Addabbo, F.4
Chiodini, P.5
Vitale, M.6
Perillo, L.7
-
32
-
-
0016774415
-
Frequency of dental trait anomalies in cleft, sibling and non-cleft groups
-
Schroeder DC, Green LJ,. 1975. Frequency of dental trait anomalies in cleft, sibling and non-cleft groups. J Dent Res. 54: 802-807.
-
(1975)
J Dent Res
, vol.54
, pp. 802-807
-
-
Schroeder, D.C.1
Green, L.J.2
-
33
-
-
84864094899
-
Mutations in WNT10A are present in more than half of isolated hypodontia cases
-
van den Boogaard MJ, Créton M, Bronkhorst Y, van der Hout A, Hennekam E, Lindhout D, Cune M, Ploos van Amstel HK,. 2012. Mutations in WNT10A are present in more than half of isolated hypodontia cases. J Med Genet. 49 (5): 327-331.
-
(2012)
J Med Genet
, vol.49
, Issue.5
, pp. 327-331
-
-
Van Den Boogaard, M.J.1
Créton, M.2
Bronkhorst, Y.3
Van Der Hout, A.4
Hennekam, E.5
Lindhout, D.6
Cune, M.7
Ploos Van Amstel, H.K.8
-
34
-
-
84555189571
-
RNAscope: A novel in situ RNA analysis platform for formalin-fixed, paraffin-embedded tissues
-
Wang F, Flanagan J, Su N, Wang LC, Bui S, Nielson A, Wu X, Vo HT, Ma Xj, Luo Y., 2012. RNAscope: a novel in situ RNA analysis platform for formalin-fixed, paraffin-embedded tissues. J Mol Diagn. 14 (1): 22-29.
-
(2012)
J Mol Diagn
, vol.14
, Issue.1
, pp. 22-29
-
-
Wang, F.1
Flanagan, J.2
Su, N.3
Wang, L.C.4
Bui, S.5
Nielson, A.6
Wu, X.7
Vo, H.T.8
Ma, X.9
Luo, Y.10
-
35
-
-
84904350279
-
Evaluation and integration of disparate classification systems for clefts of the lip
-
Wang KH, Heike CL, Clarkson MD, Mejino JL, Brinkley JF, Tse RW, Birgfeld CB, Fitzsimons DA, Cox TC,. 2014. Evaluation and integration of disparate classification systems for clefts of the lip. Front Physiol. 5: 163.
-
(2014)
Front Physiol
, vol.5
, pp. 163
-
-
Wang, K.H.1
Heike, C.L.2
Clarkson, M.D.3
Mejino, J.L.4
Brinkley, J.F.5
Tse, R.W.6
Birgfeld, C.B.7
Fitzsimons, D.A.8
Cox, T.C.9
-
36
-
-
33645814683
-
Expression profiles of cIRF6, cLHX6 and cLHX7 in the facial primordia suggest specific roles during primary palatogenesis
-
Washbourne BJ, Cox TC,. 2006. Expression profiles of cIRF6, cLHX6 and cLHX7 in the facial primordia suggest specific roles during primary palatogenesis. BMC Dev Biol. 6: 18.
-
(2006)
BMC Dev Biol
, vol.6
, pp. 18
-
-
Washbourne, B.J.1
Cox, T.C.2
-
37
-
-
84919490237
-
The molecular basis of hereditary enamel defects in humans
-
Wright JT, Carrion IA, Morris C., 2015. The molecular basis of hereditary enamel defects in humans. J Dent Res. 94 (1) 52-61.
-
(2015)
J Dent Res
, vol.94
, Issue.1
, pp. 52-61
-
-
Wright, J.T.1
Carrion, I.A.2
Morris, C.3
-
38
-
-
57449090278
-
Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4
-
Wright JT, Hart TC, Hart PS, Simmons D, Suggs C, Daley B, Simmer J, Hu J, Bartlett JD, Li Y, et al. 2009. Human and mouse enamel phenotypes resulting from mutation or altered expression of AMEL, ENAM, MMP20 and KLK4. Cells Tissues Organs. 189 (1-4): 224-229.
-
(2009)
Cells Tissues Organs
, vol.189
, Issue.1-4
, pp. 224-229
-
-
Wright, J.T.1
Hart, T.C.2
Hart, P.S.3
Simmons, D.4
Suggs, C.5
Daley, B.6
Simmer, J.7
Hu, J.8
Bartlett, J.D.9
Li, Y.10
-
39
-
-
84945115671
-
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds
-
Yang J, Wang SK, Choi M, Reid BM, Hu Y, Lee YL, Herzog CR, Kim-Berman H, Lee M, Benke PJ, et al. 2015. Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindreds. Mol Genet Genomic Med. 3 (1): 40-58.
-
(2015)
Mol Genet Genomic Med
, vol.3
, Issue.1
, pp. 40-58
-
-
Yang, J.1
Wang, S.K.2
Choi, M.3
Reid, B.M.4
Hu, Y.5
Lee, Y.L.6
Herzog, C.R.7
Kim-Berman, H.8
Lee, M.9
Benke, P.J.10
-
40
-
-
4143115809
-
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate
-
Zucchero TM, Cooper ME, Maher BS, Daack-Hirsch S, Nepomuceno B, Ribeiro L, Caprau D, Christensen K, Suzuki Y, Machida J, et al. 2004. Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolated cleft lip or palate. N Engl J Med. 351 (8): 769-780.
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(2004)
N Engl J Med
, vol.351
, Issue.8
, pp. 769-780
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Zucchero, T.M.1
Cooper, M.E.2
Maher, B.S.3
Daack-Hirsch, S.4
Nepomuceno, B.5
Ribeiro, L.6
Caprau, D.7
Christensen, K.8
Suzuki, Y.9
Machida, J.10
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