-
1
-
-
39449117834
-
-
International Clearinghouse for Birth Defects Monitoring Systems, Annual Report Rome: International Centre on Birth Defects
-
International Clearinghouse for Birth Defects Monitoring Systems, Annual Report 2003 Rome: International Centre on Birth Defects 2003
-
(2003)
Annual Report 2003
-
-
-
2
-
-
0036153367
-
National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: Investigation of genetic aetiology
-
10.1136/jmg.39.1.16 11826019
-
National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology. D Morrison D FitzPatrick I Hanson K Williamson V van Heyningen B Fleck I Jones J Chalmers H Campbell, J Med Genet 2002 39 16 22 10.1136/jmg.39.1.16 11826019
-
(2002)
J Med Genet
, vol.39
, pp. 16-22
-
-
Morrison, D.1
Fitzpatrick, D.2
Hanson, I.3
Williamson, K.4
Van Heyningen, V.5
Fleck, B.6
Jones, I.7
Chalmers, J.8
Campbell, H.9
-
3
-
-
0036053072
-
A capture-recapture model to estimate prevalence of children born in Scotland with developmental eye defects
-
10.1080/14766650252962649 12369602
-
A capture-recapture model to estimate prevalence of children born in Scotland with developmental eye defects. H Campbell E Holmes S MacDonald D Morrison I Jones, J Cancer Epidemiol Prev 2002 7 21 28 10.1080/14766650252962649 12369602
-
(2002)
J Cancer Epidemiol Prev
, vol.7
, pp. 21-28
-
-
Campbell, H.1
Holmes, E.2
MacDonald, S.3
Morrison, D.4
Jones, I.5
-
4
-
-
23344437422
-
Epidemiologic characteristics of anophthalmia and bilateral microphthalmia among 2.5 million births in California, 1989-1997
-
16007635
-
Epidemiologic characteristics of anophthalmia and bilateral microphthalmia among 2.5 million births in California, 1989-1997. GM Shaw SL Carmichael W Yang JA Harris RH Finnell EJ Lammer, Am J Med Genet A 2005 137 36 40 16007635
-
(2005)
Am J Med Genet A
, vol.137
, pp. 36-40
-
-
Shaw, G.M.1
Carmichael, S.L.2
Yang, W.3
Harris, J.A.4
Finnell, R.H.5
Lammer, E.J.6
-
5
-
-
0029861609
-
The descriptive epidemiology of anophthalmia and microphthalmia
-
10.1093/ije/25.5.1009 8921488
-
The descriptive epidemiology of anophthalmia and microphthalmia. B Kallen E Robert J Harris, Int J Epidemiol 1996 25 1009 1016 10.1093/ije/25.5.1009 8921488
-
(1996)
Int J Epidemiol
, vol.25
, pp. 1009-1016
-
-
Kallen, B.1
Robert, E.2
Harris, J.3
-
6
-
-
33645530617
-
Descriptive epidemiology of anophthalmia and microphthalmia, Hawaii, 1986-2001
-
10.1002/bdra.20237 16498668
-
Descriptive epidemiology of anophthalmia and microphthalmia, Hawaii, 1986-2001. MB Forrester RD Merz, Birth Defects Res A Clin Mol Teratol 2006 76 187 92 10.1002/bdra.20237 16498668
-
(2006)
Birth Defects Res A Clin Mol Teratol
, vol.76
, pp. 187-92
-
-
Forrester, M.B.1
Merz, R.D.2
-
9
-
-
19444369502
-
Developmental eye disorders
-
10.1016/j.gde.2005.04.013 15917212
-
Developmental eye disorders. DR Fitzpatrick V van Heyningen, Curr Opin Genet Dev 2005 15 348 353 10.1016/j.gde.2005.04.013 15917212
-
(2005)
Curr Opin Genet Dev
, vol.15
, pp. 348-353
-
-
Fitzpatrick, D.R.1
Van Heyningen, V.2
-
13
-
-
0344953586
-
Mutations in SOX2 cause anophthalmia
-
10.1038/ng1120 12612584
-
Mutations in SOX2 cause anophthalmia. JA Fantes NK Ragge SA Lynch NI McGill JRO Collin PN Howard-Peebles C Hayward AJ Vivian KA Williamson V van Heyningen DR FitzPatrick, Nat Genet 2003 33 461 463 10.1038/ng1120 12612584
-
(2003)
Nat Genet
, vol.33
, pp. 461-463
-
-
Fantes, J.A.1
Ragge, N.K.2
Lynch, S.A.3
McGill, N.I.4
Collin, J.R.O.5
Howard-Peebles, P.N.6
Hayward, C.7
Vivian, A.J.8
Williamson, K.A.9
Van Heyningen, V.10
Fitzpatrick, D.R.11
-
14
-
-
20944448656
-
SOX2 anophthalmia syndrome
-
15812812
-
SOX2 anophthalmia syndrome. NK Ragge B Lorenz A Schneider K Bushby L de Sanctis U de Sanctis A Salt JR Collin AJ Vivian SL Free P Thompson KA Williamson SM Sisodiya V van Heyningen DR Fitzpatrick, Am J Med Genet A 2005 135 1 8 15812812
-
(2005)
Am J Med Genet A
, vol.135
, pp. 1-8
-
-
Ragge, N.K.1
Lorenz, B.2
Schneider, A.3
Bushby, K.4
De Sanctis, L.5
De Sanctis, U.6
Salt, A.7
Collin, J.R.8
Vivian, A.J.9
Free, S.L.10
Thompson, P.11
Williamson, K.A.12
Sisodiya, S.M.13
Van Heyningen, V.14
Fitzpatrick, D.R.15
-
15
-
-
33646162880
-
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome
-
10.1093/hmg/ddl064 16543359
-
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome. KA Williamson AM Hever J Rainger RC Rogers A Magee Z Fiedler WT Keng FH Sharkey N McGill CJ Hill A Schneider M Messina PD Turnpenny JA Fantes V van Heyningen DR FitzPatrick, Hum Mol Genet 2006 15 1413 1422 10.1093/hmg/ddl064 16543359
-
(2006)
Hum Mol Genet
, vol.15
, pp. 1413-1422
-
-
Williamson, K.A.1
Hever, A.M.2
Rainger, J.3
Rogers, R.C.4
Magee, A.5
Fiedler, Z.6
Keng, W.T.7
Sharkey, F.H.8
McGill, N.9
Hill, C.J.10
Schneider, A.11
Messina, M.12
Turnpenny, P.D.13
Fantes, J.A.14
Van Heyningen, V.15
Fitzpatrick, D.R.16
-
16
-
-
0028074973
-
PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects
-
10.1038/ng0894-463 7951315
-
PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects. T Glaser L Jepeal JG Edwards SR Young J Favor RL Maas, Nat Genet 1994 7 463 471 10.1038/ng0894-463 7951315
-
(1994)
Nat Genet
, vol.7
, pp. 463-471
-
-
Glaser, T.1
Jepeal, L.2
Edwards, J.G.3
Young, S.R.4
Favor, J.5
Maas, R.L.6
-
17
-
-
11144263623
-
Interplay of Pax6 and SOX2 in lens development as a paradigm of genetic switch mechanisms for cell differentiation
-
10.1387/ijdb.041868hk 15558474
-
Interplay of Pax6 and SOX2 in lens development as a paradigm of genetic switch mechanisms for cell differentiation. H Kondoh M Uchikawa Y Kamachi, Int J Dev Biol 2004 48 819 827 10.1387/ijdb.041868hk 15558474
-
(2004)
Int J Dev Biol
, vol.48
, pp. 819-827
-
-
Kondoh, H.1
Uchikawa, M.2
Kamachi, Y.3
-
18
-
-
33644791152
-
Role of SOX2 mutations in human hippocampal malformations and epilepsy
-
10.1111/j.1528-1167.2006.00464.x 16529618
-
Role of SOX2 mutations in human hippocampal malformations and epilepsy. SM Sisodiya NK Ragge GL Cavalleri A Hever B Lorenz A Schneider KA Williamson JM Stevens SL Free PJ Thompson V van Heyningen DR Fitzpatrick, Epilepsia 2006 47 534 542 10.1111/j.1528-1167.2006.00464.x 16529618
-
(2006)
Epilepsia
, vol.47
, pp. 534-542
-
-
Sisodiya, S.M.1
Ragge, N.K.2
Cavalleri, G.L.3
Hever, A.4
Lorenz, B.5
Schneider, A.6
Williamson, K.A.7
Stevens, J.M.8
Free, S.L.9
Thompson, P.J.10
Van Heyningen, V.11
Fitzpatrick, D.R.12
-
19
-
-
33746492174
-
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans
-
16826526 10.1086/505654
-
Homozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humans. S Valleix F Niel B Nedelec MP Algros C Schwartz B Delbosc M Delpech B Kantelip, Am J Hum Genet 2006 79 358 364 16826526 10.1086/505654
-
(2006)
Am J Hum Genet
, vol.79
, pp. 358-364
-
-
Valleix, S.1
Niel, F.2
Nedelec, B.3
Algros, M.P.4
Schwartz, C.5
Delbosc, B.6
Delpech, M.7
Kantelip, B.8
-
20
-
-
21044452878
-
Heterozygous mutations of OTX2 cause severe ocular malformations
-
15846561 10.1086/430721
-
Heterozygous mutations of OTX2 cause severe ocular malformations. NK Ragge AG Brown CM Poloschek B Lorenz RA Henderson MP Clarke I Russell-Eggitt A Fielder D Gerrelli JP Martinez-Barbera P Ruddle J Hurst JR Collin A Salt ST Cooper PJ Thompson SM Sisodiya KA Williamson DR FitzPatrick V van Heyningen IM Hanson, Am J Hum Genet 2005 76 1008 1022 15846561 10.1086/430721
-
(2005)
Am J Hum Genet
, vol.76
, pp. 1008-1022
-
-
Ragge, N.K.1
Brown, A.G.2
Poloschek, C.M.3
Lorenz, B.4
Henderson, R.A.5
Clarke, M.P.6
Russell-Eggitt, I.7
Fielder, A.8
Gerrelli, D.9
Martinez-Barbera, J.P.10
Ruddle, P.11
Hurst, J.12
Collin, J.R.13
Salt, A.14
Cooper, S.T.15
Thompson, P.J.16
Sisodiya, S.M.17
Williamson, K.A.18
Fitzpatrick, D.R.19
Van Heyningen, V.20
Hanson, I.M.21
more..
-
21
-
-
1042268859
-
Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea
-
10.1093/hmg/ddh025 14662654
-
Mutations in the human RAX homeobox gene in a patient with anophthalmia and sclerocornea. VA Voronina EA Kozhemyakina CM O'Kernick ND Kahn SL Wenger JV Linberg AS Schneider PH Mathers, Hum Mol Genet 2004 13 315 322 10.1093/hmg/ddh025 14662654
-
(2004)
Hum Mol Genet
, vol.13
, pp. 315-322
-
-
Voronina, V.A.1
Kozhemyakina, E.A.2
O'Kernick, C.M.3
Kahn, N.D.4
Wenger, S.L.5
Linberg, J.V.6
Schneider, A.S.7
Mathers, P.H.8
-
22
-
-
0034425404
-
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10
-
10.1038/78071 10932181
-
Human microphthalmia associated with mutations in the retinal homeobox gene CHX10. E Ferda Percin LA Ploder JJ Yu K Arici DJ Horsford A Rutherford B Bapat DW Cox AM Duncan VI Kalnins A Kocak-Altintas JC Sowden E Traboulsi M Sarfarazi RR McInnes, Nat Genet 2000 25 397 401 10.1038/78071 10932181
-
(2000)
Nat Genet
, vol.25
, pp. 397-401
-
-
Ferda Percin, E.1
Ploder, L.A.2
Yu, J.J.3
Arici, K.4
Horsford, D.J.5
Rutherford, A.6
Bapat, B.7
Cox, D.W.8
Duncan, A.M.9
Kalnins, V.I.10
Kocak-Altintas, A.11
Sowden, J.C.12
Traboulsi, E.13
Sarfarazi, M.14
McInnes, R.R.15
-
24
-
-
33847215172
-
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation
-
17273977 10.1086/512203
-
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation. F Pasutto H Sticht G Hammersen G Gillessen-Kaesbach DR Fitzpatrick G Nurnberg F Brasch H Schirmer-Zimmermann JL Tolmie D Chitayat G Houge L Fernandez-Martinez S Keating G Mortier RC Hennekam A von der Wense A Slavotinek P Meinecke P Bitoun C Becker P Nurnberg A Reis A Rauch, Am J Hum Genet 2007 80 550 560 17273977 10.1086/512203
-
(2007)
Am J Hum Genet
, vol.80
, pp. 550-560
-
-
Pasutto, F.1
Sticht, H.2
Hammersen, G.3
Gillessen-Kaesbach, G.4
Fitzpatrick, D.R.5
Nurnberg, G.6
Brasch, F.7
Schirmer-Zimmermann, H.8
Tolmie, J.L.9
Chitayat, D.10
Houge, G.11
Fernandez-Martinez, L.12
Keating, S.13
Mortier, G.14
Hennekam, R.C.15
Von Der Wense, A.16
Slavotinek, A.17
Meinecke, P.18
Bitoun, P.19
Becker, C.20
Nurnberg, P.21
Reis, A.22
Rauch, A.23
more..
-
25
-
-
33749032115
-
CRYBA4, a novel human cataract gene, is also involved in microphthalmia
-
16960806 10.1086/507712
-
CRYBA4, a novel human cataract gene, is also involved in microphthalmia. G Billingsley ST Santhiya AD Paterson K Ogata S Wodak SM Hosseini SM Manisastry P Vijayalakshmi PM Gopinath J Graw E Heon, Am J Hum Genet 2006 79 702 709 16960806 10.1086/507712
-
(2006)
Am J Hum Genet
, vol.79
, pp. 702-709
-
-
Billingsley, G.1
Santhiya, S.T.2
Paterson, A.D.3
Ogata, K.4
Wodak, S.5
Hosseini, S.M.6
Manisastry, S.M.7
Vijayalakshmi, P.8
Gopinath, P.M.9
Graw, J.10
Heon, E.11
-
26
-
-
0033652303
-
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15
-
11035633 10.1086/316894
-
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15. L Morle M Bozon JC Zech N Alloisio A Raas-Rothschild C Philippe JC Lambert J Godet H Plauchu P Edery, Am J Hum Genet 2000 67 1592 1597 11035633 10.1086/316894
-
(2000)
Am J Hum Genet
, vol.67
, pp. 1592-1597
-
-
Morle, L.1
Bozon, M.2
Zech, J.C.3
Alloisio, N.4
Raas-Rothschild, A.5
Philippe, C.6
Lambert, J.C.7
Godet, J.8
Plauchu, H.9
Edery, P.10
-
27
-
-
0031971589
-
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32
-
9545413 10.1086/301843
-
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32. DA Bessant S Khaliq A Hameed K Anwar SQ Mehdi AM Payne SS Bhattacharya, Am J Hum Genet 1998 62 1113 1116 9545413 10.1086/301843
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1113-1116
-
-
Bessant, D.A.1
Khaliq, S.2
Hameed, A.3
Anwar, K.4
Mehdi, S.Q.5
Payne, A.M.6
Bhattacharya, S.S.7
-
28
-
-
0032797310
-
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32
-
10413693
-
Phenotype of autosomal recessive congenital microphthalmia mapping to chromosome 14q32. DA Bessant K Anwar S Khaliq A Hameed M Ismail AM Payne SQ Mehdi SS Bhattacharya, Br J Ophthalmol 1999 83 919 922 10413693
-
(1999)
Br J Ophthalmol
, vol.83
, pp. 919-922
-
-
Bessant, D.A.1
Anwar, K.2
Khaliq, S.3
Hameed, A.4
Ismail, M.5
Payne, A.M.6
Mehdi, S.Q.7
Bhattacharya, S.S.8
-
29
-
-
84907113316
-
X-linked clinical anophthalmos. Localization of the gene to Xq27-Xq28
-
10.3109/13816819109023084 1679229
-
X-linked clinical anophthalmos. Localization of the gene to Xq27-Xq28. CA Graham RM Redmond NC Nevin, Ophthalmic Paediatr Genet 1991 12 43 48 10.3109/13816819109023084 1679229
-
(1991)
Ophthalmic Paediatr Genet
, vol.12
, pp. 43-48
-
-
Graham, C.A.1
Redmond, R.M.2
Nevin, N.C.3
-
30
-
-
0032480566
-
Geographical variation in anophthalmia and microphthalmia in England, 1988-94
-
9756803
-
Geographical variation in anophthalmia and microphthalmia in England, 1988-94. H Dolk A Busby BG Armstrong PH Walls, BMJ 1998 317 905 909 9756803
-
(1998)
BMJ
, vol.317
, pp. 905-909
-
-
Dolk, H.1
Busby, A.2
Armstrong, B.G.3
Walls, P.H.4
-
31
-
-
0028500288
-
Anophthalmia and benomyl in Italy: A multicenter study based on 940,615 newborns
-
10.1016/0890-6238(94)90079-5 7841658
-
Anophthalmia and benomyl in Italy: a multicenter study based on 940,615 newborns. A Spagnolo F Bianchi A Calabro E Calzolari M Clementi P Mastroiacovo P Meli G Petrelli R Tenconi, Reprod Toxicol 1994 8 397 403 10.1016/0890-6238(94) 90079-5 7841658
-
(1994)
Reprod Toxicol
, vol.8
, pp. 397-403
-
-
Spagnolo, A.1
Bianchi, F.2
Calabro, A.3
Calzolari, E.4
Clementi, M.5
Mastroiacovo, P.6
Meli, P.7
Petrelli, G.8
Tenconi, R.9
-
32
-
-
0028058287
-
Clusters of anophthalmia. No link with benomyl in Italy
-
8312793
-
Clusters of anophthalmia. No link with benomyl in Italy. F Bianchi A Calabro E Calzolari PP Mastroiacovo G Petrelli A Spagnolo R Tenconi, BMJ 1994 308 205 8312793
-
(1994)
BMJ
, vol.308
, pp. 205
-
-
Bianchi, F.1
Calabro, A.2
Calzolari, E.3
Mastroiacovo, P.P.4
Petrelli, G.5
Spagnolo, A.6
Tenconi, R.7
-
33
-
-
0028772882
-
Clusters of anophthalmia. or in Norway
-
8312794
-
Clusters of anophthalmia. or in Norway. P Kristensen LM Irgens, BMJ 1994 308 205 206 8312794
-
(1994)
BMJ
, vol.308
, pp. 205-206
-
-
Kristensen, P.1
Irgens, L.M.2
-
34
-
-
84907112423
-
An update on microphthalmos and coloboma. A brief survey of genetic disorders with microphthalmos and coloboma
-
10.3109/13816819109023675 1923314
-
An update on microphthalmos and coloboma. A brief survey of genetic disorders with microphthalmos and coloboma. M Warburg, Ophthalmic Paediatr Genet 1991 12 57 63 10.3109/13816819109023675 1923314
-
(1991)
Ophthalmic Paediatr Genet
, vol.12
, pp. 57-63
-
-
Warburg, M.1
-
35
-
-
0023132648
-
Parvovirus B19 associated with fetal abnormality
-
10.1016/S0140-6736(87)90442-9 2882099
-
Parvovirus B19 associated with fetal abnormality. HT Weiland C Vermey-Keers MM Salimans GJ Fleuren RA Verwey MJ Anderson, Lancet 1987 1 8534 682 683 10.1016/S0140-6736(87)90442-9 2882099
-
(1987)
Lancet
, vol.1
, Issue.8534
, pp. 682-683
-
-
Weiland, H.T.1
Vermey-Keers, C.2
Salimans, M.M.3
Fleuren, G.J.4
Verwey, R.A.5
Anderson, M.J.6
-
39
-
-
33645302939
-
Bilateral aplasia of the optic nerve, chiasm, and tracts in an otherwise healthy infant
-
10.1136/bjo.2005.088229 16547339
-
Bilateral aplasia of the optic nerve, chiasm, and tracts in an otherwise healthy infant. MS Sanjari K Ghasemi Falavarjani MM Parvaresh HH Kharazi MB Kashkooli, Br J Ophthalmol 2006 90 513 514 10.1136/bjo.2005.088229 16547339
-
(2006)
Br J Ophthalmol
, vol.90
, pp. 513-514
-
-
Sanjari, M.S.1
Ghasemi Falavarjani, K.2
Parvaresh, M.M.3
Kharazi, H.H.4
Kashkooli, M.B.5
-
40
-
-
18644367029
-
Bilateral congenital anophthalmos and agenesis of the optic pathways
-
15861506
-
Bilateral congenital anophthalmos and agenesis of the optic pathways. M Aktekin O Oz MR Saygili Z Kurtoglu, Yonsei Med J 2005 46 296 299 15861506
-
(2005)
Yonsei Med J
, vol.46
, pp. 296-299
-
-
Aktekin, M.1
Oz, O.2
Saygili, M.R.3
Kurtoglu, Z.4
-
41
-
-
33644857728
-
Recurrence of SOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal mother
-
16470798
-
Recurrence of SOX2 anophthalmia syndrome with gonosomal mosaicism in a phenotypically normal mother. L Faivre KA Williamson V Faber N Laurent M Grimaldi C Thauvin-Robinet C Durand F Mugneret JB Gouyon A Bron F Huet C Hayward V Heyningen DR Fitzpatrick, Am J Med Genet A 2006 140 636 639 16470798
-
(2006)
Am J Med Genet A
, vol.140
, pp. 636-639
-
-
Faivre, L.1
Williamson, K.A.2
Faber, V.3
Laurent, N.4
Grimaldi, M.5
Thauvin-Robinet, C.6
Durand, C.7
Mugneret, F.8
Gouyon, J.B.9
Bron, A.10
Huet, F.11
Hayward, C.12
Heyningen, V.13
Fitzpatrick, D.R.14
-
42
-
-
7944225563
-
Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2
-
10.1002/pd.997 15503273
-
Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2. A Guichet S Triau C Lepinard C Esculapavit F Biquard P Descamps F Encha-Razavi D Bonneau, Prenat Diagn 2004 24 828 832 10.1002/pd.997 15503273
-
(2004)
Prenat Diagn
, vol.24
, pp. 828-832
-
-
Guichet, A.1
Triau, S.2
Lepinard, C.3
Esculapavit, C.4
Biquard, F.5
Descamps, P.6
Encha-Razavi, F.7
Bonneau, D.8
-
43
-
-
0026022766
-
First- and second-trimester diagnosis of fetal ocular defects and associated anomalies: Report of eight cases
-
1992414
-
First- and second-trimester diagnosis of fetal ocular defects and associated anomalies: report of eight cases. M Bronshtein E Zimmer R Gershoni-Baruch N Yoffe H Meyer Z Blumenfeld, Obstet Gynecol 1991 77 443 449 1992414
-
(1991)
Obstet Gynecol
, vol.77
, pp. 443-449
-
-
Bronshtein, M.1
Zimmer, E.2
Gershoni-Baruch, R.3
Yoffe, N.4
Meyer, H.5
Blumenfeld, Z.6
-
44
-
-
0042090352
-
Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging
-
10.1002/uog.135 12905522
-
Prenatal diagnosis of otocephaly with microphthalmia/anophthalmia using ultrasound and magnetic resonance imaging. CP Chen KG Wang JK Huang TY Chang YH Lin DT Chin CY Tzen W Wang, Ultrasound Obstet Gynecol 2003 22 214 215 10.1002/uog.135 12905522
-
(2003)
Ultrasound Obstet Gynecol
, vol.22
, pp. 214-215
-
-
Chen, C.P.1
Wang, K.G.2
Huang, J.K.3
Chang, T.Y.4
Lin, Y.H.5
Chin, D.T.6
Tzen, C.Y.7
Wang, W.8
-
46
-
-
33646079161
-
Early and late onset fetal microphthalmia
-
10.1016/j.ajog.2005.11.010 16647921
-
Early and late onset fetal microphthalmia. S Blazer EZ Zimmer E Mezer M Bronshtein, Am J Obstet Gynecol 2006 194 1354 1359 10.1016/j.ajog.2005.11.010 16647921
-
(2006)
Am J Obstet Gynecol
, vol.194
, pp. 1354-1359
-
-
Blazer, S.1
Zimmer, E.Z.2
Mezer, E.3
Bronshtein, M.4
-
48
-
-
13944263697
-
Integrated reconstructive strategies for treating the anophthalmic orbit
-
15458669
-
Integrated reconstructive strategies for treating the anophthalmic orbit. L Clauser E Sarti V Dallera M Galiè J Craniomaxillofac Surg 2004 32 279 290 15458669
-
(2004)
J Craniomaxillofac Surg
, vol.32
, pp. 279-290
-
-
Clauser, L.1
Sarti, E.2
Dallera, V.3
Galiè, M.4
-
49
-
-
0015452667
-
Growth retardation and volume determinations of the anophthalmic orbit
-
Growth retardation and volume determinations of the anophthalmic orbit. RE Kennedy, Trans Am Ophthalmol Soc 1972 70 277 297
-
(1972)
Trans Am Ophthalmol Soc
, vol.70
, pp. 277-297
-
-
Kennedy, R.E.1
-
50
-
-
34247493682
-
The Effect of Early Enucleation on the Orbit in Animals and Humans
-
14269905
-
The Effect of Early Enucleation on the Orbit in Animals and Humans. RE Kennedy, Trans Am Ophthalmol Soc 1964 62 459 510 14269905
-
(1964)
Trans Am Ophthalmol Soc
, vol.62
, pp. 459-510
-
-
Kennedy, R.E.1
-
52
-
-
33846392841
-
Evaluation of an integrated orbital tissue expander in an anophthalmic feline model
-
10.1016/j.ajo.2006.10.028 17169319
-
Evaluation of an integrated orbital tissue expander in an anophthalmic feline model. DT Tse L Pinchuk S Davis SF Falcone W Lee AC Acosta E Hernandez E Lee JM Parel, Am J Ophthalmol 2007 143 317 327 10.1016/j.ajo.2006.10.028 17169319
-
(2007)
Am J Ophthalmol
, vol.143
, pp. 317-327
-
-
Tse, D.T.1
Pinchuk, L.2
Davis, S.3
Falcone, S.F.4
Lee, W.5
Acosta, A.C.6
Hernandez, E.7
Lee, E.8
Parel, J.M.9
-
53
-
-
0038798840
-
The management of orbital cysts associated with congenital microphthalmos and anophthalmos
-
12812886 10.1136/bjo.87.7.860
-
The management of orbital cysts associated with congenital microphthalmos and anophthalmos. CJ McLean NK Ragge RB Jones JR Collin, Br J Ophthalmol 2003 87 860 863 12812886 10.1136/bjo.87.7.860
-
(2003)
Br J Ophthalmol
, vol.87
, pp. 860-863
-
-
McLean, C.J.1
Ragge, N.K.2
Jones, R.B.3
Collin, J.R.4
|