244 related articles for article (PubMed ID: 20145385)
1. 'Pure' partial trisomy 4q26-->q35.2 resulting from a familial unbalanced translocation t(4;10)(q26;q26.3).
Zhang YL; Dai Y; Tu ZG; Li QY
Cytogenet Genome Res; 2009; 127(1):67-72. PubMed ID: 20145385
[TBL] [Abstract][Full Text] [Related]
2. [Cytogenetic and molecular characterization of partial trisomy 4q and partial monosomy 10q in a patient].
Zhang YL; Dai Y; Tu ZG; Li QY; Wang LQ; Zhang L; Zeng J; Ouyang ZB
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Apr; 27(2):153-7. PubMed ID: 20376795
[TBL] [Abstract][Full Text] [Related]
3. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
4. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
5. High risk for unbalanced segregation of some reciprocal translocations: a large pedigree containing distal 4q trisomy from t(4;7)(q28;p22).
Francisco-Bagnariolli AM; Payão SL; Kawasaki-Oyama RS; Sabbag Filho D; Segato R; de Labio RW; Chauffaille ML; Priest JH
Am J Med Genet; 2001 Nov; 103(4):302-7. PubMed ID: 11746010
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [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]
8. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
Schürmann M; Wethling H; Niemeyer ML; Schwinger E
Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
[TBL] [Abstract][Full Text] [Related]
9. [Translocation trisomy 4q in 2 siblings as a sequela of paternal balanced reciprocal translocation: t(1;4)(q44;q31)].
Bode H; Bühler EM; Wyler F; Hadzilselimovic F
Monatsschr Kinderheilkd; 1990 Nov; 138(11):763-6. PubMed ID: 2290435
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. "Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation.
Mikelsaar RV; Lurie IW; Ilus TE
J Med Genet; 1996 Apr; 33(4):344-5. PubMed ID: 8730295
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. Pure partial trisomy 5q33-->5q35 resulting from the adjacent-1 segregation of a paternal (5;14)(q33;p12) translocation.
Paoloni-Giacobino A; Bottani A; Dahoun SP
Ann Genet; 1999; 42(3):166-9. PubMed ID: 10526660
[TBL] [Abstract][Full Text] [Related]
14. Subtelomeric familial translocation t(2;7)(q37;q35) leading to partial trisomy 7q35-->qter: molecular cytogenetic analysis and clinical phenotype in two generations.
Speleman F; Callens B; Logghe K; Van Roy N; Horsley SW; Jauch A; Verschraegen-Spae MR; Leroy JG
Am J Med Genet; 2000 Aug; 93(5):349-54. PubMed ID: 10951456
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Partial trisomy 4q due to a maternal translocation: t(4;18)(q27;q21.31).
Van Buggenhout G; Moerman PH; Fryns JP
Genet Couns; 1997; 8(1):19-24. PubMed ID: 9101274
[TBL] [Abstract][Full Text] [Related]
17. A subtle familial translocation t(3;21)(p26.3;q22.3): an apparently healthy boy with a 3p deletion and 21q duplication.
Gijsbers AC; van Haeringen A; Bosch CA; Hansson K; Verschuren M; Bakker E; Breuning MH; Ruivenkamp CA
Cytogenet Genome Res; 2010 Jun; 128(4):245-9. PubMed ID: 20431279
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
19. Pure partial trisomy 4q syndrome in a child with der(9)ins(9;4)(q34.3;q26q35.2)mat.
Topcu V; Ilgin-Ruhi H; Yurur-Kutlay N; Ekici C; Vicdan A; Tukun FA
Genet Couns; 2014; 25(1):1-6. PubMed ID: 24783648
[TBL] [Abstract][Full Text] [Related]
20. Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature.
Brisset S; Joly G; Ozilou C; Lapierre JM; Gosset P; LeLorc'h M; Raoul O; Turleau C; Vekemans M; Romana SP
Am J Med Genet; 2002 Dec; 113(4):339-45. PubMed ID: 12457405
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
