365 related articles for article (PubMed ID: 19761709)
1. Distal trisomy of 10q with distal monosomy of 15q due to a paternal translocation.
Sun SC; Luo FW; Song HW; He JB; Peng YS
J Int Med Res; 2009; 37(4):1230-7. PubMed ID: 19761709
[TBL] [Abstract][Full Text] [Related]
2. Chromosomal 10Q26 trisomy resulting from paternal T(9;10)(PTER;Q26.1).
Hou JW
J Formos Med Assoc; 2003 Dec; 102(12):887-92. PubMed ID: 14976570
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
4. Partial monosomy 10q and partial trisomy 9q with anal atresia due to maternal translocation: t(9;10)(q32;q26).
Tsukuda T; Nagata I; Sawada H; Murakami J; Hanaki K; Urashima H; Kaneda T; Shimizu N; Kaibara N; Kodama N; Ohzeki T; Shiraki K
Clin Genet; 1996 Oct; 50(4):220-2. PubMed ID: 9001803
[TBL] [Abstract][Full Text] [Related]
5. Rapid aneuploidy diagnosis of partial trisomy 7q (7q34→qter) and partial monosomy 10q (10q26.12→qter) by array comparative genomic hybridization using uncultured amniocytes.
Chen CP; Lin SP; Su YN; Tsai FJ; Wu PC; Town DD; Chen LF; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2012 Mar; 51(1):93-9. PubMed ID: 22482977
[TBL] [Abstract][Full Text] [Related]
6. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
8. Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities.
Cox DM; Butler MG
Cytogenet Genome Res; 2015; 145(1):29-34. PubMed ID: 25871641
[TBL] [Abstract][Full Text] [Related]
9. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
10. Distal trisomy 10q/partial monosomy 14q: an unusual clinical picture.
Bregant L; Gersak K; Veble A
Genet Couns; 2005; 16(1):59-63. PubMed ID: 15844780
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result.
Chen CP; Ko TM; Wang LK; Chern SR; Wu PS; Chen SW; Wu FT; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2021 Jul; 60(4):775-777. PubMed ID: 34247824
[TBL] [Abstract][Full Text] [Related]
12. Partial monosomy of 10p and duplication of another chromosome in two patients.
Ohta S; Isojima T; Mizuno Y; Kato M; Mimaki M; Seki M; Sato Y; Ogawa S; Takita J; Kitanaka S; Oka A
Pediatr Int; 2017 Jan; 59(1):99-102. PubMed ID: 28102624
[TBL] [Abstract][Full Text] [Related]
13. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
[TBL] [Abstract][Full Text] [Related]
14. [4p trisomy secondary to paternal translocation t(4p-;15q+)].
Saad A; Khelif M; Kharrat H; Bouzakoura C
Ann Pediatr (Paris); 1991 May; 38(5):350-4. PubMed ID: 1872531
[TBL] [Abstract][Full Text] [Related]
15. [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. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
16. Partial trisomy 2q(2q37.3-->qter) and monosomy 7q(7q34--->qter) due to paternal reciprocal translocation 2;7: a case report.
Ahn JM; Koo DH; Kwon KW; Lee YK; Lee YH; Lee HH; Nam KH; Lee KH
J Korean Med Sci; 2003 Feb; 18(1):112-3. PubMed ID: 12589098
[TBL] [Abstract][Full Text] [Related]
17. Monosomy 10q26-qter and trisomy 11q13-qter as a result of de novo unbalanced translocation.
Tinsa F; Chebbi Y; Meddeb M; Bousnina D; Boussetta K; Bousnina S
J Appl Genet; 2009; 50(3):289-91. PubMed ID: 19638686
[TBL] [Abstract][Full Text] [Related]
18. [Chromosome aberration in a full-term neonate with low birth weight using microarray comparative genomic hybridization].
Sun S; Luo F; He J; Chen W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):550-4. PubMed ID: 18841570
[TBL] [Abstract][Full Text] [Related]
19. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: description in a boy with partial trisomy 10q and monosomy 4q and review of the literature.
Bartholdi D; Toelle SP; Steiner B; Boltshauser E; Schinzel A; Riegel M
Eur J Med Genet; 2008; 51(2):113-23. PubMed ID: 18262484
[TBL] [Abstract][Full Text] [Related]
20. Familial partial trisomy of the long arm of chromosome 10 (q24-26).
Moreno-Fuenmayor H; Zackai EH; Mellman WJ; Aronson M
Pediatrics; 1975 Nov; 56(5):756-61. PubMed ID: 1196732
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]