280 related articles for article (PubMed ID: 8839892)
21. [Partial 10q trisomy (q24;q ter) caused by a balanced maternal translocation t(6;10)(q26;q24)].
Aledo AG; Gracia R; López Pajares I; González M; Oliver A; Peralta A
An Esp Pediatr; 1982 Aug; 17(2):125-9. PubMed ID: 7149479
[TBL] [Abstract][Full Text] [Related]
22. Diaphragmatic hernia and Fryns syndrome phenotype in partial trisomy 22.
de Beaufort C; Schneider F; Chafai R; Colette JM; Delneste D; Pierquin G
Genet Couns; 2000; 11(2):181-2. PubMed ID: 10893671
[No Abstract] [Full Text] [Related]
23. Further delineation of 7p trisomy. Case report and review of literature.
Pallotta R; Dalprà L; Fusilli P; Zuffardi O
Ann Genet; 1996; 39(3):152-8. PubMed ID: 8839888
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Maternal origin of extra marker chromosome 1Q31.1-qter and 13pter-q12.12 in a child with dysmorhic features.
Rao VB; Kerketta L; Korgaonkar S; Ghosh K; Mohanty D
Genet Couns; 2005; 16(2):139-43. PubMed ID: 16082769
[TBL] [Abstract][Full Text] [Related]
26. Terminal deletion of the long arm of chromosome 10: a new case with breakpoint in q25.3.
Petersen B; Strassburg HM; Feichtinger W; Kress W; Schmid M
Am J Med Genet; 1998 Apr; 77(1):60-2. PubMed ID: 9557896
[TBL] [Abstract][Full Text] [Related]
27. NFkappaB2 gene duplication is associated with fetal pyelectasis in partial trisomy 10q (10q24.1 --> qter).
Chen CP; Chen YJ; Tsai FJ; Chern SR; Wang W
Prenat Diagn; 2008 Apr; 28(4):364-5. PubMed ID: 18383001
[No Abstract] [Full Text] [Related]
28. Unbalanced translocation (3;5)(q26.1;p14): a clinical report.
Rossi M; Di Micco P; Perone L; De Brasi D; Guzzetta V; Andreucci MV; Vega GR; Marzano MG; Iaccarino E; Andria G
Am J Med Genet; 2002 Jul; 110(4):353-8. PubMed ID: 12116209
[TBL] [Abstract][Full Text] [Related]
29. A distinct phenotype associated with partial trisomy 10q due to proximal direct duplication 10q11 --> q223?
van Buggenhout G; Decock P; Fryns JP
Genet Couns; 1996; 7(1):53-9. PubMed ID: 8652089
[TBL] [Abstract][Full Text] [Related]
30. Sacrococcygeal teratoma in a fetus with prenatally diagnosed partial trisomy 10q (10q24.3-->qter) and partial monosomy 17p (p13.3-->pter).
Batukan C; Ozgun MT; Basbug M; Caglayan O; Dundar M; Murat N
Prenat Diagn; 2007 Apr; 27(4):365-8. PubMed ID: 17295347
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Partial proximal trisomy 10q syndrome: a new case.
Nucaro A; Faedda A; Cao A; Boccone L
Genet Couns; 2002; 13(4):411-6. PubMed ID: 12558111
[TBL] [Abstract][Full Text] [Related]
33. Further delineation of pseudotrisomy 13 syndrome: a case without polydactyly.
Ramos-Arroyo MA; de Miguel C; Valiente A; Moreno-Laguna S
Am J Med Genet; 1994 Apr; 50(2):177-9. PubMed ID: 8010349
[TBL] [Abstract][Full Text] [Related]
34. Partial trisomy 9--further delineation of the phenotype.
Smart RD; Viljoen DL; Fraser B
Am J Med Genet; 1988 Dec; 31(4):947-51. PubMed ID: 3239584
[TBL] [Abstract][Full Text] [Related]
35. Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.
Mishra R; Paththinige CS; Sirisena ND; Nanayakkara S; Kariyawasam UGIU; Dissanayake VHW
BMC Pediatr; 2018 Jan; 18(1):4. PubMed ID: 29310616
[TBL] [Abstract][Full Text] [Related]
36. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
37. Combined trisomy 9P and Shprintzen syndrome resulting from a paternal t(9;22).
Komatsu H; Kihara A; Komura E; Mitsufuji N; Tsujii H; Kakita S; Ikuta H
Genet Couns; 2001; 12(2):137-43. PubMed ID: 11491308
[TBL] [Abstract][Full Text] [Related]
38. FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.
Chu TW; Teebi AS; Gibson L; Breg WR; Yang-Feng TL
Am J Med Genet; 1994 Aug; 52(1):92-6. PubMed ID: 7977471
[TBL] [Abstract][Full Text] [Related]
39. Simultaneous trisomy 10q24 leads to qter and monosomy 4p16: an example of epistasis at the chromosome level.
Cantu JM; Hernandez A; Nazara Z; Rolon A; Ramirez ML; Sanchez-Corona J; Rivera H
Ann Genet; 1981; 24(1):41-4. PubMed ID: 6971617
[TBL] [Abstract][Full Text] [Related]
40. [Clinical and molecular cytogenetic analysis of a rare case of mosaicism for partial monosomy 3p and partial trisomy 10q in human].
Karamysheva TV; Matveeva VG; Shorina AP; Rubtsov NB
Genetika; 2001 Jun; 37(6):811-6. PubMed ID: 11517768
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]