187 related articles for article (PubMed ID: 25867311)
1. Postnatal diagnosis of constitutive ring chromosome 13 using both conventional and molecular cytogenetic approaches.
Minasi LB; Pinto IP; de Almeida JG; de Melo AV; Cunha DM; Ribeiro CL; Silva GP; Brasil MG; Silva DM; da Silva CC; da Cruz AD
Genet Mol Res; 2015 Mar; 14(1):1692-9. PubMed ID: 25867311
[TBL] [Abstract][Full Text] [Related]
2. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
[TBL] [Abstract][Full Text] [Related]
3. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[TBL] [Abstract][Full Text] [Related]
4. [Chromosome analysis and phenotype location analysis on a patient with the karyotype of 45, XX, -13/46, XX, r(13)/46, XX, r(13;13)/47, XX, 2r(13)(p13q32.3)].
Liang DS; Wu LQ; Long ZG; Pan Q; Dai HP; Xia JH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):392-4. PubMed ID: 15300643
[TBL] [Abstract][Full Text] [Related]
5. 13q Deletion and central nervous system anomalies: further insights from karyotype-phenotype analyses of 14 patients.
Ballarati L; Rossi E; Bonati MT; Gimelli S; Maraschio P; Finelli P; Giglio S; Lapi E; Bedeschi MF; Guerneri S; Arrigo G; Patricelli MG; Mattina T; Guzzardi O; Pecile V; Police A; Scarano G; Larizza L; Zuffardi O; Giardino D
J Med Genet; 2007 Jan; 44(1):e60. PubMed ID: 17209130
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
[TBL] [Abstract][Full Text] [Related]
7. Molecular and cytogenetic characterisation of an unusual case of partial trisomy/partial monosomy 13 mosaicism: 46,XX,r(13)(p11q14)/46,XX,der(13)t(13;13)(q10;q14).
Gentile M; Buonadonna AL; Cariola F; Fiorente P; Valenzano MC; Guanti G
J Med Genet; 1999 Jan; 36(1):77-82. PubMed ID: 9950374
[TBL] [Abstract][Full Text] [Related]
8. Genotype-phenotype correlation in 13q13.3-q21.3 deletion.
Tosca L; Brisset S; Petit FM; Metay C; Latour S; Lautier B; Lebas A; Druart L; Picone O; Mas AE; Prévot S; Tardieu M; Goossens M; Tachdjian G
Eur J Med Genet; 2011; 54(5):e489-94. PubMed ID: 21741501
[TBL] [Abstract][Full Text] [Related]
9. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
10. Mosaic r(13) resulting in large deletion of chromosome 13q in a newborn female with multiple congenital anomalies.
Lorentz CP; Jalal SM; Thompson DM; Babovic-Vuksanovic D
Am J Med Genet; 2002 Jul; 111(1):61-7. PubMed ID: 12124737
[TBL] [Abstract][Full Text] [Related]
11. Clinical, cytogenetic and molecular study in a case of r(3) with 3p deletion and review of the literature.
Guilherme RS; Bragagnolo S; Pellegrino R; Christofolini DM; Takeno SS; Carvolheira GM; Kulikowski LD; Melaragno MI
Cytogenet Genome Res; 2011; 134(4):325-30. PubMed ID: 21849783
[TBL] [Abstract][Full Text] [Related]
12. [Analysis of ring chromosome 9 syndrome with fluorescence in situ hybridization].
Ye ZC; Zhu XY; Zhao R; He XY; Zhang HJ; Li LP; Zhu YM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Oct; 27(5):559-62. PubMed ID: 20931537
[TBL] [Abstract][Full Text] [Related]
13. Transmission of ring chromosome 13 from a mother to daughter with both having a 46,XX, r(13)(p13q34) karyotype.
Bedoyan JK; Flore LA; Alkatib A; Ebrahim SA; Bawle EV
Am J Med Genet A; 2004 Sep; 129A(3):316-20. PubMed ID: 15326636
[TBL] [Abstract][Full Text] [Related]
14. 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay.
Rodovalho-Doriqui MJ; Freitas PL; Pinho JD; Cavalli LR; Pereira SR
Genet Mol Res; 2013 Jul; 12(3):2562-6. PubMed ID: 23979887
[TBL] [Abstract][Full Text] [Related]
15. Mosaic deletion-duplication syndrome of chromosome 3: prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy.
Chen CP; Su YN; Hsu CY; Chern SR; Lee CC; Chen YT; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):485-91. PubMed ID: 22212322
[TBL] [Abstract][Full Text] [Related]
16. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
Zhu XY; Zhao R; Ye ZC; Peng YG; Tan YQ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec; 22(6):682-3. PubMed ID: 16331572
[TBL] [Abstract][Full Text] [Related]
17. 22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS.
Alp MY; Çebi AH; Seyhan S; Cansu A; Aydin H; Ikbal M
Genet Couns; 2016; 27(1):43-9. PubMed ID: 27192891
[TBL] [Abstract][Full Text] [Related]
18. Smallest critical region for microcephaly in a patient with mosaic ring chromosome 13.
Su PH; Chen CP; Su YN; Chen SJ; Lin LL; Chen JY
Genet Mol Res; 2013 Apr; 12(2):1311-7. PubMed ID: 23661454
[TBL] [Abstract][Full Text] [Related]
19. [Molecular cytogenetic detection of partial chromosome 13q trisomy and its relation with the clinical features of tortilcollis].
Du J; Tan YQ; Li LY; Lu GX
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Jun; 20(3):189-92. PubMed ID: 12778440
[TBL] [Abstract][Full Text] [Related]
20. An unusual chromosome 22q11 deletion associated with an apparent complementary ring chromosome in a phenotypically normal woman.
Toutain J; Taine L; Morice-Picard F; Hallal H; Dai ZQ; Arveiler B; Lacombe D; Horovitz J; Saura R
Eur J Med Genet; 2011; 54(3):292-4. PubMed ID: 21215339
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]