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Items: 1 to 20 of 135

1.

Clinical and cytogenetic study of a non mosaic 46, X, isodicentric Yq in an Egyptian patient with Turner syndrome.

El-Bassyouni HT, El-Gerzawy A, Eid O, El-Ruby MO.

Genet Couns. 2013;24(1):37-44.

PMID:
23610863
2.

[Analysis of the small supernumerary marker chromosome in Turner syndrome with 45, X/46, X, + mar karyotype].

Ye ZC, Cai JG, Zhu XY, Zhao R, He XY, Zhong Y, Liu KX, Zhu YM.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Aug;26(4):461-4. Chinese.

PMID:
20017317
3.

[Identification of the small supernumerary marker chromosomes in two patients with Turner syndrome].

Wen J, Liang D, Liao X, Xue J, Tang G, Xia Y, Long Z, Dai H, Wu L.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2009 Dec;26(6):659-63. doi: 10.3760/cma.j.issn.1003-9406.2009.06.011. Chinese.

PMID:
19953489
4.

[Identification and characterization of marker chromosome in Turner syndrome].

Tan YQ, Cheng DH, DI YF, Li LY, Lu GX.

Zhonghua Fu Chan Ke Za Zhi. 2007 Oct;42(10):679-82. Chinese.

PMID:
18241543
5.

Molecular and cytogenetic characterization of a non-mosaic isodicentric Y chromosome in a patient with Klinefelter syndrome.

Heinritz W, Kotzot D, Heinze S, Kujat A, Kleemann WJ, Froster UG.

Am J Med Genet A. 2005 Jan 15;132A(2):198-201.

PMID:
15578587
6.

[Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization].

Liang Y, Luo XP.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2005 Aug;22(4):435-7. Chinese.

PMID:
16086285
7.

Double aneuploidy in three Egyptian patients: Down-Turner and Down-Klinefelter syndromes.

Zaki MS, Kamel AA, El-Ruby M.

Genet Couns. 2005;16(4):393-402.

PMID:
16440882
8.

Analysis of Turner syndrome patients within the Jordanian population, with a focus on four patients with Y chromosome abnormalities.

Daggag H, Srour W, El-Khateeb M, Ajlouni K.

Sex Dev. 2013;7(6):295-302. doi: 10.1159/000354279. Epub 2013 Aug 29.

PMID:
23988405
9.

Isodicentric Y chromosomes in Egyptian patients with disorders of sex development (DSD).

Mekkawy M, Kamel A, El-Ruby M, Mohamed A, Essawi M, Soliman H, Dessouky N, Shehab M, Mazen I.

Am J Med Genet A. 2012 Jul;158A(7):1594-603. doi: 10.1002/ajmg.a.35487. Epub 2012 May 24.

PMID:
22628100
10.

Gonadoblastoma in patients with Ullrich-Turner syndrome.

Zelaya G, López Marti JM, Marino R, Garcia de Dávila MT, Gallego MS.

Pediatr Dev Pathol. 2015 Mar-Apr;18(2):117-21. doi: 10.2350/14-08-1539-OA.1. Epub 2014 Dec 23.

PMID:
25535833
11.

Evidence of a mechanism for isodicentric chromosome Y formation in a 45,X/46,X,idic(Y)(p11.31)/46,X,del(Y)(p11.31) mosaic karyotype.

Reshmi SC, Miller JL, Deplewski D, Close C, Henderson LJ, Littlejohn E, Schwartz S, Waggoner DJ.

Eur J Med Genet. 2011 Mar-Apr;54(2):161-4. doi: 10.1016/j.ejmg.2010.11.002. Epub 2010 Nov 13.

PMID:
21078420
12.

Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.

Polityko AD, Khurs OM, Kulpanovich AI, Mosse KA, Solntsava AV, Rumyantseva NV, Naumchik IV, Liehr T, Weise A, Mkrtchyan H.

Eur J Med Genet. 2009 Jul-Aug;52(4):207-10. doi: 10.1016/j.ejmg.2009.03.016. Epub 2009 Apr 16.

PMID:
19375526
13.

[The inclusion of new techniques of chromosome analysis has improved the cytogenetic profile of Turner syndrome].

Barros BA, Maciel-Guerra AT, De Mello MP, Coeli FB, Carvalho AB, Viguetti-Campos N, Assumpção Jde G, Marques-de-Faria AP, Lemos-Marini SH, Guerra-Junior G.

Arq Bras Endocrinol Metabol. 2009 Dec;53(9):1137-42. Portuguese.

14.

FISH and PCR analyses in three patients with 45,X/46,X,idic(Y) karyotype: clinical and pathologic spectrum.

Alvarez-Nava F, Soto M, Martínez MC, Prieto M, Alvarez Z.

Ann Genet. 2003 Oct-Dec;46(4):443-8.

PMID:
14659779
15.

Different chromosome Y abnormalities in Turner syndrome.

Bağci G, Acar H, Tomruk H.

Genet Couns. 2001;12(3):255-61.

PMID:
11693789
16.

A Turner-like phenotype in a girl with an isodicentric fluorescent Y chromosome mosaicism.

Bergendi E, Plöchl E, Vlasak I, Rittinger O, Muss W.

Klin Padiatr. 1997 May-Jun;209(3):133-6.

PMID:
9183775
17.

Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.

Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E.

Eur J Med Genet. 2006 Mar-Apr;49(2):141-9. Epub 2005 Jul 1.

PMID:
16530711
18.

FISH analysis helps identify low-level mosaicism in Ullrich-Turner syndrome patients.

Wiktor A, Van Dyke DL.

Genet Med. 2004 May-Jun;6(3):132-5.

PMID:
15354330
19.

Mosaic Turner syndrome: cytogenetics versus FISH.

Abulhasan SJ, Tayel SM, al-Awadi SA.

Ann Hum Genet. 1999 May;63(Pt 3):199-206.

PMID:
10738532
20.

Mixed gonadal dysgenesis in a child with isodicentric Y chromosome: Does the relative proportion of the 45,X line really matter?

Shinawi M, Cain MP, Vanderbrink BA, Grignon DJ, Mensing D, Cooper ML, Bader P, Cheung SW.

Am J Med Genet A. 2010 Jul;152A(7):1832-7. doi: 10.1002/ajmg.a.33475.

PMID:
20583182

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