122 related articles for article (PubMed ID: 2667459)
1. De novo dir dup (1)(q3200----4200) in an adult. Further delineation of the pure 1q trisomy syndrome.
Barros-Núñez P; Sánchez-Corona J; Rolón A; Medina C; García-Ochoa C; García-Cruz MO; Nazará Z; García-Cruz D
Ann Genet; 1989; 32(2):97-101. PubMed ID: 2667459
[TBL] [Abstract][Full Text] [Related]
2. Zygodactyly as the most striking physical anomaly in an adult male patient with pure partial trisomy 1q.
Lukusa T; Van Buggenhout G; Devriendt K; Meireleire J; Van Goethem G; Roelen L; Fryns JP
Ann Genet; 1998; 41(4):199-204. PubMed ID: 9881182
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 1q (1q32-->1qter) in adulthood: further delineation of the phenotype.
Van Buggenhout G; De Coen L; Fryns JP
Ann Genet; 1998; 41(2):77-81. PubMed ID: 9706337
[TBL] [Abstract][Full Text] [Related]
4. Borderline intelligence and discrete craniofacial dysmorphism in an adolescent female with partial trisomy 7p due to a de novo tandem duplication 7 (p15.1-->p21.3).
Kleczkowska A; Decock P; van den Berghe H; Fryns JP
Genet Couns; 1994; 5(4):393-7. PubMed ID: 7888144
[No Abstract] [Full Text] [Related]
5. Partial trisomy 13q22----qter. A new case.
Galán F; García R; Aguilar MS; Moya M
Ann Genet; 1989; 32(2):114-6. PubMed ID: 2757360
[TBL] [Abstract][Full Text] [Related]
6. Acrocallosal syndrome in a child with de novo inverted tandem duplication of 12p11.2-p13.3.
Pfeiffer RA; Legat G; Trautmann U
Ann Genet; 1992; 35(1):41-6. PubMed ID: 1610119
[TBL] [Abstract][Full Text] [Related]
7. Dup(1q)(q42-->qter) syndrome: case report and review of literature.
Kennerknecht I; Barbi G; Rodens K
Am J Med Genet; 1993 Dec; 47(8):1157-60. PubMed ID: 7507296
[TBL] [Abstract][Full Text] [Related]
8. Partial distal 1q trisomy. A distinct clinical dysmorphic syndrome in adulthood.
Fryns JP; de Muelenaere A; Pedersen J; Van Den Berghe H
Ann Genet; 1980; 23(3):181-2. PubMed ID: 6968537
[TBL] [Abstract][Full Text] [Related]
9. The phenotypic and cytogenetic spectrum of partial trisomy 9.
Wilson GN; Raj A; Baker D
Am J Med Genet; 1985 Feb; 20(2):277-82. PubMed ID: 3976721
[TBL] [Abstract][Full Text] [Related]
10. Trisomy (1q)(q42----qter): confirmation of a syndrome.
Chia NL; Bousfield LR; Poon CC; Trudinger BJ
Clin Genet; 1988 Oct; 34(4):224-9. PubMed ID: 3233776
[TBL] [Abstract][Full Text] [Related]
11. Trisomy 7p due to a mosaic normal/dir dup(7)(p13----p22). Syndrome delineation, critical segment assignment, and a comment on duplications.
Cantú JM; Rivas F; Ruiz C; Barajas LO; Moller M; Rivera H
Ann Genet; 1985; 28(4):254-7. PubMed ID: 3879442
[TBL] [Abstract][Full Text] [Related]
12. Extreme growth failure and kyphoscoliosis as complications of the distal trisomy 10q syndrome.
Soekarman D; Fryns JP
Genet Couns; 1992; 3(2):111-3. PubMed ID: 1642808
[TBL] [Abstract][Full Text] [Related]
13. First report of a partial trisomy 3q12-q23 de novo--FISH breakpoint determination and phenotypic characterization.
Gamerdinger U; Bosse K; Eggermann T; Kalscheuer V; Schwanitz G; Engels H
Eur J Med Genet; 2006; 49(3):225-34. PubMed ID: 16762824
[TBL] [Abstract][Full Text] [Related]
14. Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): further delineation of trisomies 1q.
Bartsch C; Aslan M; Köhler J; Miny P; Horst J; Holzgreve W; Rehder H; Fritz B
Fetal Diagn Ther; 2001; 16(5):265-73. PubMed ID: 11509847
[TBL] [Abstract][Full Text] [Related]
15. [Partial trisomy 3q. Contribution of a new case to the literature].
Elorza Arizmendi JF; Amor Trucios J; Fayos Soler JL; Ferriols Gil E; Romero Andreu I; Tacóns Mateu J
An Esp Pediatr; 1989 May; 30(5):391-3. PubMed ID: 2667414
[No Abstract] [Full Text] [Related]
16. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome?
Redha MA; Krishna Murthy DS; al-Awadi SA; al-Sulaiman IS; Sabry MA; el-Bahey SA; Farag TI
Ann Genet; 1996; 39(1):5-9. PubMed ID: 9297445
[TBL] [Abstract][Full Text] [Related]
17. [Trisomy for distal segments of the long arm of chromosome 1].
Lur'e IV; Kodunov LA; Veropotvelian NP; Rumiantseva NV; Zaletaev DV; Belik MG
Genetika; 1989 Dec; 25(12):2251-5. PubMed ID: 2634579
[TBL] [Abstract][Full Text] [Related]
18. Trisomy 1q42 --> qter in a sister and brother: further delineation of the "trisomy 1q42 --> qter syndrome".
Verschuuren-Bemelmans CC; Leegte B; Hodenius TM; Cobben JM
Am J Med Genet; 1995 Jul; 58(1):83-6. PubMed ID: 7573162
[TBL] [Abstract][Full Text] [Related]
19. Silver-Russell phenotype in a patient with pure trisomy 1q32.1-q42.1: further delineation of the pure 1q trisomy syndrome.
van Haelst MM; Eussen HJ; Visscher F; de Ruijter JL; Drop SL; Lindhout D; Wouters CH; Govaerts LC
J Med Genet; 2002 Aug; 39(8):582-5. PubMed ID: 12161598
[No Abstract] [Full Text] [Related]
20. 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]
[Next] [New Search]
