Similar articles for PMID: 10564870

Year	Number of Results
1974	1
1977	1
1978	1
1979	1
1982	1
1984	1
1985	1
1987	3
1988	4
1989	4
1991	4
1992	2
1993	4
1994	2
1995	3
1996	4
1997	4
1998	4
1999	5
2000	2
2002	4
2003	3
2004	6
2005	1
2006	4
2007	5
2008	1
2009	3
2011	2
2012	3
2013	2
2014	3
2015	3
2017	1
2018	2
2019	3
2021	1
2024	0

1

Isolated bilateral anophthalmia in a girl with an apparently balanced de novo translocation: 46,XX,t(3;11)(q27;p11.2).

Driggers RW, Macri CJ, Greenwald J, Carpenter D, Avallone J, Howard-Peebles PN, Levin SW. Driggers RW, et al. Am J Med Genet. 1999 Nov 26;87(3):201-2. doi: 10.1002/(sici)1096-8628(19991126)87:3<201::aid-ajmg1>3.0.co;2-h. Am J Med Genet. 1999. PMID: 10564870 Review.

2

Delineation of an estimated 6.7 MB candidate interval for an anophthalmia gene at 3q26.33-q28 and description of the syndrome associated with visible chromosome deletions of this region.

Male A, Davies A, Bergbaum A, Keeling J, FitzPatrick D, Mackie Ogilvie C, Berg J. Male A, et al. Eur J Hum Genet. 2002 Dec;10(12):807-12. doi: 10.1038/sj.ejhg.5200890. Eur J Hum Genet. 2002. PMID: 12461687

3

Prenatal diagnosis of primary anophthalmia with a 3q27 interstitial deletion involving SOX2.

Guichet A, Triau S, Lépinard C, Esculapavit C, Biquard F, Descamps P, Encha-Razavi F, Bonneau D. Guichet A, et al. Prenat Diagn. 2004 Oct;24(10):828-32. doi: 10.1002/pd.997. Prenat Diagn. 2004. PMID: 15503273

4

Detection of structural abnormalities in spermatozoa of a translocation carrier t(3;11)(q27.3;q24.3) by triple FISH.

Martini E, von Bergh AR, Coonen E, de Die-Smulders CE, Hopman AH, Ramaekers FC, Geraedts JP. Martini E, et al. Hum Genet. 1998 Feb;102(2):157-65. doi: 10.1007/s004390050670. Hum Genet. 1998. PMID: 9521583

5

Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)].

Chitayat D, Babul R, Silver MM, Jay V, Teshima IE, Babyn P, Becker LE. Chitayat D, et al. Am J Med Genet. 1996 Jan 2;61(1):45-8. doi: 10.1002/(SICI)1096-8628(19960102)61:1<45::AID-AJMG9>3.0.CO;2-W. Am J Med Genet. 1996. PMID: 8741917 Review.

6

[Bilateral anophthalmos. Facial anomalies and t(4;14) translocation].

Serville F, Broustet A, Peyresblanques J, Bouineau J. Serville F, et al. J Genet Hum. 1974 Dec;22(4):341-51. J Genet Hum. 1974. PMID: 4461763 French. No abstract available.

7

Congenital arhinia with de novo reciprocal translocation, t(3;12)(q13.2;p11.2).

Hou JW. Hou JW. Am J Med Genet A. 2004 Oct 1;130A(2):200-3. doi: 10.1002/ajmg.a.30268. Am J Med Genet A. 2004. PMID: 15372519

8

Bilateral microphthalmos with colobomatous orbital cyst and de-novo balanced translocation t(3;5).

Kurbasic M, Jones FV, Cook LN. Kurbasic M, et al. Ophthalmic Genet. 2000 Dec;21(4):239-42. Ophthalmic Genet. 2000. PMID: 11135495

9

Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome.

Williamson KA, Hever AM, Rainger J, Rogers RC, Magee A, Fiedler Z, Keng WT, Sharkey FH, McGill N, Hill CJ, Schneider A, Messina M, Turnpenny PD, Fantes JA, van Heyningen V, FitzPatrick DR. Williamson KA, et al. Hum Mol Genet. 2006 May 1;15(9):1413-22. doi: 10.1093/hmg/ddl064. Epub 2006 Mar 16. Hum Mol Genet. 2006. PMID: 16543359

10

Mosaicism for trisomy 3q arising from an unbalanced, de novo t(3;15).

Stallings R, Vaughn D, Hall K, Joyce C, Ryan F, Barton D, Geraghty M. Stallings R, et al. J Med Genet. 1997 Jun;34(6):512-4. doi: 10.1136/jmg.34.6.512. J Med Genet. 1997. PMID: 9192276 Free PMC article.

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