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Results: 1 to 20 of 115

Similar articles for PubMed (Select 23406309)

1.

Ophthalmologic observations in a patient with partial mosaic trisomy 8.

Abu-Amero KK, Kondkar AA, Salih MA, Al-Husain M, Al Shammari M, Zeidan G, Oystreck DT, Hellani AM, Kentab AY, Bosley TM.

Ophthalmic Genet. 2013 Dec;34(4):249-53. doi: 10.3109/13816810.2012.762933. Epub 2013 Feb 13.

PMID:
23406309
2.

Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.

Eyüpoğlu FC, Sünnetçi D, Cine N, Savli H, Okten A, Açikgöz EG, Sönmez FM.

Genet Couns. 2014;25(3):305-13.

PMID:
25365853
3.
4.

Prenatal diagnosis of mosaic trisomy 8q studied by ultrasound, cytogenetics, and array-CGH.

Wood E, Dowey S, Saul D, Cain C, Rossiter J, Blakemore K, Stetten G.

Am J Med Genet A. 2008 Mar 15;146A(6):764-9. doi: 10.1002/ajmg.a.32184.

PMID:
18241063
5.

Coexistence of neurofibromatosis type 1 and mosaic trisomy 8 in the same patient.

Basaran SY, Sensoy V, Kiroglu K, Messiaen L, Tuysuz B.

Genet Couns. 2010;21(3):307-16.

PMID:
20964122
6.

Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.

Machado IN, Heinrich JK, Campanhol C, Rodrigues-Peres RM, Oliveira FM, Barini R.

Genet Mol Res. 2010 Mar 16;9(1):441-8. doi: 10.4238/vol9-1gmr716.

7.

Are Duane syndrome and infantile esotropia allelic?

Connell BJ, Wilkinson RM, Barbour JM, Scotter LW, Poulsen JL, Wirth MG, Essex RW, Savarirayan R, Mackey DA.

Ophthalmic Genet. 2004 Sep;25(3):189-98.

PMID:
15512995
8.

[Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].

Zhu CJ, Huang ZY, Wu WQ, Zhao Q, Jiang HY, Xie JS.

Zhonghua Er Ke Za Zhi. 2012 Jun;50(6):460-4. Chinese.

PMID:
22931946
9.

A rare case: mosaic trisomy 22.

Basaran N, Berkil H, Ay N, Durak B, Ataman C, Ozdemir M, Ozon YH, Kaya I.

Ann Genet. 2001 Oct-Dec;44(4):183-6.

PMID:
11755102
10.

Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.

van Balkom ID, Hagendoorn J, De Pater JM, Hennekam RC.

Genet Couns. 1992;3(2):83-9. Review.

PMID:
1642815
11.

Partial trisomy 8 mosaicism due to a pseudoisodicentric chromosome 8.

Leon E, Jamal SM, Zou YS, Milunsky JM.

Am J Med Genet A. 2011 Jul;155A(7):1740-4. doi: 10.1002/ajmg.a.34073. Epub 2011 Jun 10.

PMID:
21671393
12.

Partial trisomy 8 mosaicism not detected by cultured amniotic-fluid cells.

Tsai MC, Cheng HY, Su MT, Chen M, Kuo PL.

Taiwan J Obstet Gynecol. 2014 Dec;53(4):598-601. doi: 10.1016/j.tjog.2014.06.003.

PMID:
25510708
13.

Array-CGH study of partial trisomy 9p without mental retardation.

Bouhjar IB, Hannachi H, Zerelli SM, Labalme A, Gmidène A, Soyah N, Missaoui S, Sanlaville D, Elghezal H, Saad A.

Am J Med Genet A. 2011 Jul;155A(7):1735-9. doi: 10.1002/ajmg.a.34044. Epub 2011 May 27.

PMID:
21626676
14.

[Mosaic trisomy 9: report of a new case with a long-term survival].

Sánchez Zahonero J, Andrés Celma M, López García MJ.

An Pediatr (Barc). 2008 Mar;68(3):273-6. Spanish.

15.

Secondary trisomy or mosaic "tetrasomy" 8p.

Robinow M, Haney N, Chen H, Sorauf T, Van Dyke DL, Babu VR, Powell S, Maliszewski W, Guerin S, Landers JW.

Am J Med Genet. 1989 Mar;32(3):320-4.

PMID:
2729351
16.

[Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].

Xiao B, Zhang JM, Ji X, Jiang WT, Hu J, Tao J.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Jun;28(3):247-50. doi: 10.3760/cma.j.issn.1003-9406.2011.03.002. Chinese.

PMID:
21644216
17.

A case with mosaic partial duplication of 1q: prenatal and postmortem clinical and cytogenetic evaluations.

Karaoguz MY, Biri A, Pala E, Kan D, Poyraz A, Kurdoglu M, Percin EF.

Genet Couns. 2006;17(2):197-204.

PMID:
16970038
18.

Partial mosaic trisomy 5: a new case report with ocular involvement.

Schlegel Z, Valent A, Hirsch A.

J Fr Ophtalmol. 2009 Oct;32(8):533-9. doi: 10.1016/j.jfo.2009.06.004. Epub 2009 Aug 6.

19.

Paternal origin of der(X)t(X;6) in a girl with trisomy 6p and unbalanced t(6;10) mosaicism in her mother.

Petković I, Barisić I, Bastić M, Hećimović S, Bago R.

Am J Med Genet A. 2003 Jul 15;120A(2):266-71.

PMID:
12833412
20.

[Maternal toxoplasma infection and mosaic trisomy 8 syndrome].

Morava E, Varga L, Czakó M, Decsi T.

Orv Hetil. 2002 Mar 17;143(11):563-5. Hungarian.

PMID:
12583326
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