204 related articles for article (PubMed ID: 26430900)
1. 47,XY,+der(X)t(X;18)(p11.4;p11.22): A Unique Aneuploidy Associated with Klinefelter Syndrome due to an Extra Derivative X Chromosome Inherited Maternally.
Liang J; Zhang Y; Wang R; Liang Z; Yue J; Liu R
Cytogenet Genome Res; 2015; 146(3):204-10. PubMed ID: 26430900
[TBL] [Abstract][Full Text] [Related]
2. Beckwith-Wiedemann syndrome due to 11p15.5 paternal duplication associated with Klinefelter syndrome and a "de novo" pericentric inversion of chromosome Y.
Delicado A; Lapunzina P; Palomares M; Molina MA; Galán E; López Pajares I
Eur J Med Genet; 2005; 48(2):159-66. PubMed ID: 16053907
[TBL] [Abstract][Full Text] [Related]
3. Mosaic status in lymphocytes of infertile men with or without Klinefelter syndrome.
Lenz P; Luetjens CM; Kamischke A; Kühnert B; Kennerknecht I; Nieschlag E
Hum Reprod; 2005 May; 20(5):1248-55. PubMed ID: 15665007
[TBL] [Abstract][Full Text] [Related]
4. A variant Klinefelter syndrome patient with an XXY/XX/XY karyotype studied by GTG-banding and fluorescence in situ hybridization.
Mark HF; Bai H; Sotomayor E; Mark S; Zolnierz K; Airall E; Sigman M
Exp Mol Pathol; 1999 Sep; 67(1):50-6. PubMed ID: 10493892
[TBL] [Abstract][Full Text] [Related]
5. Klinefelter syndrome and other sex chromosomal aneuploidies.
Visootsak J; Graham JM
Orphanet J Rare Dis; 2006 Oct; 1():42. PubMed ID: 17062147
[TBL] [Abstract][Full Text] [Related]
6. 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. PubMed ID: 16440882
[TBL] [Abstract][Full Text] [Related]
7. Cytogenetic, Molecular, and Phenotypic Characterization of a Patient with de novo Derivative Chromosome 18 and Review of the Literature.
Gökpınar İli E; Altıner Ş; Karabulut HG
Cytogenet Genome Res; 2019; 159(2):74-80. PubMed ID: 31658462
[TBL] [Abstract][Full Text] [Related]
8. Double aneuploidy in a Turkish child: Down-Klinefelter syndrome.
Karaman A; Kabalar E
Congenit Anom (Kyoto); 2008 Mar; 48(1):45-7. PubMed ID: 18230121
[TBL] [Abstract][Full Text] [Related]
9. [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. PubMed ID: 21644216
[TBL] [Abstract][Full Text] [Related]
10. A simple screening method for detection of Klinefelter syndrome and other X-chromosome aneuploidies based on copy number of the androgen receptor gene.
Ottesen AM; Garn ID; Aksglaede L; Juul A; Rajpert-De Meyts E
Mol Hum Reprod; 2007 Oct; 13(10):745-50. PubMed ID: 17720778
[TBL] [Abstract][Full Text] [Related]
11. Unravelling the parental origin and mechanism of formation of the 47,XY,i(X)(q10) Klinefelter karyotype variant.
Höckner M; Pinggera GM; Günther B; Sergi C; Fauth C; Erdel M; Kotzot D
Fertil Steril; 2008 Nov; 90(5):2009.e13-7. PubMed ID: 18687426
[TBL] [Abstract][Full Text] [Related]
12. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
Chen CP; Chern SR; Chen CY; Wu PC; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):479-84. PubMed ID: 22212321
[TBL] [Abstract][Full Text] [Related]
13. [A de novo partial 5p deletion and cryptic 18p duplication detected by SNP-Array in a boy featuring Cri du Chat syndrome].
Hu JC; Tan K; Cheng DH; Li LY; Lu GX; Tan YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb; 30(1):87-90. PubMed ID: 23450488
[TBL] [Abstract][Full Text] [Related]
14. Tetrasomy 18p Case Report.
He Y; Liao JJ; Liu YL; Wen J; Lou JW
Clin Lab; 2020 Jan; 66(1):. PubMed ID: 32013361
[TBL] [Abstract][Full Text] [Related]
15. A case of a rare variant of Klinefelter syndrome, 47,XY,i(X)(q10).
Kondo T; Kuroda S; Usui K; Mori K; Asai T; Takeshima T; Kawahara T; Hamanoue H; Uemura H; Yumura Y
Andrologia; 2018 Sep; 50(7):e13024. PubMed ID: 29665107
[TBL] [Abstract][Full Text] [Related]
16. A rare case in literature: Isochromosome Xq in Klinefelter syndrome.
Simsek L; Zamani AG; Taskapu HH; Yildirim MS
Andrologia; 2019 Jun; 51(5):e13253. PubMed ID: 30746732
[TBL] [Abstract][Full Text] [Related]
17. Chromosomal variants in klinefelter syndrome.
Frühmesser A; Kotzot D
Sex Dev; 2011; 5(3):109-23. PubMed ID: 21540567
[TBL] [Abstract][Full Text] [Related]
18. Sperm aneuploidy in fathers of children with paternally and maternally inherited Klinefelter syndrome.
Eskenazi B; Wyrobek AJ; Kidd SA; Lowe X; Moore D; Weisiger K; Aylstock M
Hum Reprod; 2002 Mar; 17(3):576-83. PubMed ID: 11870106
[TBL] [Abstract][Full Text] [Related]
19. 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; 52(4):207-10. PubMed ID: 19375526
[TBL] [Abstract][Full Text] [Related]
20. Methylation-specific PCR allows for fast diagnosis of X chromosome disomy and reveals skewed inactivation of the X chromosome in men with Klinefelter syndrome.
Mehta A; Malek-Jones M; Bolyakov A; Mielnik A; Schlegel PN; Paduch DA
J Androl; 2012; 33(5):955-62. PubMed ID: 22441764
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]