187 related articles for article (PubMed ID: 12439894)
1. Identification of a neocentromere in a rearranged Y chromosome with no detectable DYZ3 centromeric sequence.
Assumpção JG; Berkofsky-Fessler W; Viguetti Campos N; Trevas Maciel-Guerra A; Li S; Melaragno MI; Palandi de Mello M; Warburton PE
Am J Med Genet; 2002 Dec; 113(3):263-7. PubMed ID: 12439894
[TBL] [Abstract][Full Text] [Related]
2. 47,X,idic(Y),inv dup(Y): a non-mosaic case of a phenotypically normal boy with two different Y isochromosomes and neocentromere formation.
Pasantes JJ; Wimmer R; Knebel S; Münch C; Kelbova C; Junge A; Kieback P; Küpferling P; Schempp W
Cytogenet Genome Res; 2012; 136(2):157-62. PubMed ID: 22286088
[TBL] [Abstract][Full Text] [Related]
3. [Screening for Y chromosome sequences in patients with Turner syndrome].
Ferrão L; Lopes ML; Limbert C; Marques B; Boieiro F; Silva M; Marques R; Lavinha J; Mota A; Gonçalves J
Acta Med Port; 2002; 15(2):89-100. PubMed ID: 15524154
[TBL] [Abstract][Full Text] [Related]
4. [Delineation of three structural Y chromosome aberrations combined molecular techniques].
Tu XD; Zeng J; Cong XW; Yan AZ; Huang WJ; Lin YH; Zheng DZ; Zhang M; Wang ZH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):420-4. PubMed ID: 23926008
[TBL] [Abstract][Full Text] [Related]
5. A 45,X sterile male with Yp disguised as 21p.
Dávalos IP; Rivera H; Vásquez AI; Gutiérrez-Angulo M; Hernández-Vázquez MC; Cortina-Luna FA; Wong-Ley LE; Domínguez-Quezada MG
Am J Med Genet; 2002 Aug; 111(2):202-4. PubMed ID: 12210351
[TBL] [Abstract][Full Text] [Related]
6. Identification and molecular cytogenetic characterization of a novel complex Y chromosome rearrangement in a boy with disorder of sexual development.
Dutta UR; Pidugu VK; Goud ChV; Hoefers C; Hagemann M; Dalal A
Gene; 2013 May; 519(2):374-80. PubMed ID: 23428792
[TBL] [Abstract][Full Text] [Related]
7. A neocentromere in the DAZ region of the human Y chromosome.
Floridia G; Gimelli G; Zuffardi O; Earnshaw WC; Warburton PE; Tyler-Smith C
Chromosoma; 2000; 109(5):318-27. PubMed ID: 11007490
[TBL] [Abstract][Full Text] [Related]
8. Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis.
Hernando C; Carrera M; Ribas I; Parear N; Baraibar R; Egocue J; Fuster C
Prenat Diagn; 2002 Sep; 22(9):802-5. PubMed ID: 12224075
[TBL] [Abstract][Full Text] [Related]
9. Unique (Y;13) translocation in a male with oligozoospermia: cytogenetic and molecular studies.
Alves C; Carvalho F; Cremades N; Sousa M; Barros A
Eur J Hum Genet; 2002 Aug; 10(8):467-74. PubMed ID: 12111641
[TBL] [Abstract][Full Text] [Related]
10. Cytogenetic and molecular investigations of an abnormal Y chromosome: evidence for a pseudo-dicentric (Yq) isochromosome.
Savary JB; Vasseur F; Flactif M; Willatt L; Lefebvre J; Ferguson-Smith MA; Deminatti MM
Ann Genet; 1992; 35(3):134-9. PubMed ID: 1466561
[TBL] [Abstract][Full Text] [Related]
11. Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.
Reddy KS; Sulcova V; Schwartz S; Noble JE; Phillips J; Brasel JA; Huff K; Lin HJ
Am J Med Genet; 2000 May; 92(1):69-76. PubMed ID: 10797426
[TBL] [Abstract][Full Text] [Related]
12. Neocentromere formation in a stable ring 1p32-p36.1 chromosome.
Slater HR; Nouri S; Earle E; Lo AW; Hale LG; Choo KH
J Med Genet; 1999 Dec; 36(12):914-8. PubMed ID: 10593999
[TBL] [Abstract][Full Text] [Related]
13. Molecular breakpoint analysis and relevance of variable mosaicism in a woman with short stature, primary amenorrhea, unilateral gonadoblastoma, and a 46,X,del(Y)(q11)/45,X karyotype.
Kotzot D; Dufke A; Tzschach A; Baeckert-Sifeddine IT; Geppert M; Holland H; Florus JM; Froster UG
Am J Med Genet; 2002 Sep; 112(1):51-5. PubMed ID: 12239720
[TBL] [Abstract][Full Text] [Related]
14. Identification of an unusual marker chromosome by spectral karyotyping.
Huang B; Ning Y; Lamb AN; Sandlin CJ; Jamehdor M; Ried T; Bartley J
Am J Med Genet; 1998 Dec; 80(4):368-72. PubMed ID: 9856565
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of mos46,X,del(Y)(q11.2)/45,X by cytogenetic and molecular studies with multiplex STR analysis.
Hwa HL; Ko TM; Chang YY; Huang CH; Su YN; Tseng LH; Hsieh FJ
Prenat Diagn; 2004 Feb; 24(2):121-4. PubMed ID: 14974120
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 20p resulting from inverted duplication and neocentromere formation.
Voullaire L; Saffery R; Davies J; Earle E; Kalitsis P; Slater H; Irvine DV; Choo KH
Am J Med Genet; 1999 Aug; 85(4):403-8. PubMed ID: 10398268
[TBL] [Abstract][Full Text] [Related]
17. [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. PubMed ID: 16086285
[TBL] [Abstract][Full Text] [Related]
18. Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, + mar by use of chromosome-specific DNA probes.
Lin CC; Meyne J; Sasi R; Bowen P; Unger T; Tainaka T; Hadro TA; Hoo JJ
Am J Med Genet; 1990 Sep; 37(1):71-8. PubMed ID: 2240047
[TBL] [Abstract][Full Text] [Related]
19. Fine mapping of an isodicentric Y chromosomal breakpoint from a schizophrenic patient.
Yoshitsugu K; Meerabux JM; Asai K; Yoshikawa T
Am J Med Genet B Neuropsychiatr Genet; 2003 Jan; 116B(1):27-31. PubMed ID: 12497609
[TBL] [Abstract][Full Text] [Related]
20. Characterization of an analphoid, neocentromere-positive inv dup 8p marker chromosome using multiplex whole chromosome and sub-telomere FISH analyses.
Velinov M; Gu H; Genovese M; Duncan C; Warburton P; Brooks SS; Jenkins EC
Ann Genet; 2004; 47(2):199-205. PubMed ID: 15183754
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
