409 related articles for article (PubMed ID: 2705479)
1. New chromosome aberration: duplication of a large part of chromosome 4q and partial deletion of chromosome 1q.
Merlob P; Kohn G; Litwin A; Nissenkorn I; Katznelson MB; Reisner SH
Am J Med Genet; 1989 Jan; 32(1):22-6. PubMed ID: 2705479
[TBL] [Abstract][Full Text] [Related]
2. De novo translocation involving chromosomes 1 and 4 resulting in partial duplication of 4q and partial deletion of 1p.
Legare JM; Sekhon GS; Laxova R
Am J Med Genet; 1994 Nov; 53(3):216-21. PubMed ID: 7856655
[TBL] [Abstract][Full Text] [Related]
3. Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes.
Angle B; Yen F; Hersh JH; Gowans G; Barch M
Am J Med Genet; 2002 Aug; 111(3):307-12. PubMed ID: 12210328
[TBL] [Abstract][Full Text] [Related]
4. Familial t (4;21)(q2.4;q2.2) leading to unbalanced offspring with partial duplication of 4q and of 21q without manifestations of the Down syndrome.
Kitsiou-Tzeli S; Hallett JJ; Atkins L; Latt SA; Holmes LB
Am J Med Genet; 1984 Aug; 18(4):725-9. PubMed ID: 6237580
[TBL] [Abstract][Full Text] [Related]
5. Translocation/duplication of 9p onto a duplicated 4q.
Rivera H; Figuera LE; Vasquez AI
Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
[TBL] [Abstract][Full Text] [Related]
6. Child with deletion of 4q and duplication of 1q.
Wade J; Morgan T; Allanson J
Am J Med Genet; 1989 Aug; 33(4):553-4. PubMed ID: 2596517
[No Abstract] [Full Text] [Related]
7. Double chromosome anomaly: interstitial deletion 5q and reciprocal translocation (1;11)(p22;q21).
de Michelena MI; Villacorta J; Chávez J
Am J Med Genet; 1990 May; 36(1):29-32. PubMed ID: 2185634
[TBL] [Abstract][Full Text] [Related]
8. Clinical variability of partial duplication 1q: a clinical report and literature review.
Rosenthal J; Abeliovich D; Carmi R
Am J Med Genet; 1987 Aug; 27(4):787-92. PubMed ID: 3122569
[TBL] [Abstract][Full Text] [Related]
9. Duplication 4q associated with chronic cholestatic changes in liver biopsy.
Egritas O; Cavdarli B; Dalgic B; Ergun MA; Percin F; Ziegler M; Pohle B; Liehr T
Eur J Med Genet; 2010; 53(6):411-4. PubMed ID: 20826235
[TBL] [Abstract][Full Text] [Related]
10. Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies.
Courtens W; Petersen MB; Noël JC; Flament-Durand J; Van Regemorter N; Delneste D; Cochaux P; Verschraegen-Spae MR; Van Roy N; Speleman F
Am J Med Genet; 1994 Jul; 51(3):260-5. PubMed ID: 8074156
[TBL] [Abstract][Full Text] [Related]
11. Partial 4q duplication due to inherited der(20), t(4;20)(q25;q13)mat.
Sparkes RS; Francke U; Muller H; Toomey K
Ann Genet; 1977 Mar; 20(1):31-5. PubMed ID: 302670
[TBL] [Abstract][Full Text] [Related]
12. Unbalanced mosaic karyotypes with different structural abnormalities involving a common chromosome region: report of two cases.
Pettenati MJ; Teot LA; Smith C; Hayworth R; Thomas IT; Veille JC; Rao PN
Am J Med Genet; 1993 Feb; 45(3):365-9. PubMed ID: 8434625
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Multiple congenital anomalies due to partial 2p13----2pter duplication resulting from an unbalanced X;2 translocation.
Sarda P; Lefort G; Devaux P; Humeau C; Rieu D
Ann Genet; 1992; 35(2):117-20. PubMed ID: 1524409
[TBL] [Abstract][Full Text] [Related]
15. 46,XX,der(2)t(2;10)(2pter-->2q37::10p13-->10pter)[127]/45,X,der(2)t(2;10) (2pter-->2q37::10p13-->10pter)[23]. Karyotype-phenotype correlation and genetic counselling in complex karyotypes.
Grammatico P; Majore S; Marrocco G; Poscente M; Mordenti C; Grammatico B; Del Porto G
Genet Couns; 1999; 10(4):351-8. PubMed ID: 10631922
[TBL] [Abstract][Full Text] [Related]
16. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
Pérez-Castillo A; Martin-Lucas MA; Abrisqueta JA
Ann Genet; 1990; 33(2):121-3. PubMed ID: 2241087
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. An unusual clinical characterization of a male with distal partial trisomy 1q42.1 and monosomy 4q35.1 and review of the literature.
Wang CB; Lin SP; Chen CP; Chen YJ; Lee CC
Genet Couns; 2006; 17(4):435-40. PubMed ID: 17375530
[TBL] [Abstract][Full Text] [Related]
19. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
20. Interstitial deletion of the distal long arm of chromosome 4, del (4)(q33-q35), in association with paternal balanced translocation.
Mdzin R; Ko C; Abdul Latif Z; Zakaria Z
Singapore Med J; 2008 Nov; 49(11):e336-9. PubMed ID: 19037546
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
