205 related articles for article (PubMed ID: 1872531)
1. [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]
2. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
3. A 3p deletion syndrome in a child with both del(3)(p25-->pter) and dup(17)(q23-->qter).
Lukusa T; Devriendt K; Fryns JP
Ann Genet; 1999; 42(2):91-4. PubMed ID: 10434122
[TBL] [Abstract][Full Text] [Related]
4. [Distal 14q trisomy].
Turleau C; de Grouchy J; Chavin-Colin F; Denavit MF; Le Touzé P
Ann Genet; 1983; 26(3):165-70. PubMed ID: 6606379
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. [The phenotype of the trisomy of the short arm of chromosome no. 4. (a new case with t (4p; 11q) (author's transl)].
Kessel E; Pfeiffer RA; Kosenow W
Klin Padiatr; 1976 May; 188(3):215-9. PubMed ID: 945417
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Trisomy for the distal segment of the short arm of chromosome 17 in a boy with mild mental retardation and some dysmorphic features.
Mégarbané A; Souraty N; Theophile D; Vekemans M; Samaras L; Ghorayeb Z
Ann Genet; 1997; 40(1):55-9. PubMed ID: 9150851
[TBL] [Abstract][Full Text] [Related]
10. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
Qumsiyeh MB; Stevens CA
Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
[TBL] [Abstract][Full Text] [Related]
11. Characterization of a derivative chromosome 17 by fish-technique.
Ramesh KH; Shah HO; Sherman J; Lin JH; Verma RS
Ann Genet; 1996; 39(3):177-80. PubMed ID: 8839891
[TBL] [Abstract][Full Text] [Related]
12. '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]
13. [Trisomy 4p as result of a maternal translocation t(4;8)(q11;p23)].
Stumm M; Reuter M; Mandon U; Brückner R; Wieacker P
Klin Padiatr; 1999; 211(1):35-9. PubMed ID: 10067217
[TBL] [Abstract][Full Text] [Related]
14. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. A rec(4) dup 4p inherited from a maternal inv(4)(p15q35): case report and review.
Garcia-Heras J; Martin J
Am J Med Genet; 2002 May; 109(3):226-30. PubMed ID: 11977183
[TBL] [Abstract][Full Text] [Related]
17. Monosomy and trisomy of 15q24-qter with cleft lip and palate.
Abe A; Hatano Y; Kurita K; Nakano M; Shimizu M; Yokoi T; Sugiyama N
Int J Oral Maxillofac Surg; 2008 May; 37(5):487-90. PubMed ID: 18262763
[TBL] [Abstract][Full Text] [Related]
18. Trisomy 22: no longer an enigma.
Kukolich MK; Kulharya A; Jalal SM; Drummond-Borg M
Am J Med Genet; 1989 Dec; 34(4):541-4. PubMed ID: 2624265
[TBL] [Abstract][Full Text] [Related]
19. Duplication 2q33 leads to 2q37 due to paternal ins (12;2) translocation.
Dennis NR; Neu RL; Bannerman RM
Am J Med Genet; 1978; 1(3):271-7. PubMed ID: 677166
[TBL] [Abstract][Full Text] [Related]
20. Partial monosomy 11q and trisomy 12q: variable expression in two siblings.
Lukusa T; Holvoet M; Vermeesch JR; Devriendt K; Fryns JP
Genet Couns; 2003; 14(2):155-64. PubMed ID: 12872809
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
