109 related articles for article (PubMed ID: 2757360)
21. Trisomy for the distal part of the short arm of chromosome 3.
Lurie IW; Korotkova IA; Zaletajev DV; Smirnova LI; Podlechshuk LV; Gurevich DB
Helv Paediatr Acta; 1986 Mar; 41(6):509-13. PubMed ID: 3583774
[TBL] [Abstract][Full Text] [Related]
22. Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the 'trisomy 1q42-->qter syndrome'.
Coccé MC; Villa O; Obregon MG; Salido M; Barreiro C; Solé F; Gallego MS
Cytogenet Genome Res; 2007; 118(1):84-6. PubMed ID: 17901705
[TBL] [Abstract][Full Text] [Related]
23. A case of Alagille's syndrome with translocation (4;14) (q21;q21).
Mujica P; Morali A; Vidailhet M; Pierson M; Gilgenkrantz S
Ann Genet; 1989; 32(2):117-9. PubMed ID: 2757361
[TBL] [Abstract][Full Text] [Related]
24. Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: delineation of a new syndrome.
Tuschl K; Fritz B; Herle M; Fonatsch C; Bodamer OA
Am J Med Genet A; 2007 Sep; 143A(17):2065-9. PubMed ID: 17676599
[No Abstract] [Full Text] [Related]
25. 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]
26. 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]
27. Monosomy 9p24-->pter and trisomy 5q31-->qter: case report and review of two cases.
Schimmenti LA; Higgins RR; Mendelsohn NJ; Casey TM; Steinberger J; Mammel MC; Wiesner GL
Am J Med Genet; 1995 May; 57(1):52-6. PubMed ID: 7645598
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Interstitial deletion of (17)(p11.2p11.2): report of six additional patients with a new chromosome deletion syndrome.
Stratton RF; Dobyns WB; Greenberg F; DeSana JB; Moore C; Fidone G; Runge GH; Feldman P; Sekhon GS; Pauli RM
Am J Med Genet; 1986 Jul; 24(3):421-32. PubMed ID: 3728561
[TBL] [Abstract][Full Text] [Related]
30. ["De novo" partial trisomy 16p (author's transl)].
Gabarrón Llamas J; Cabrerizo Portero D; Montserrat Bernal F; Rodríguez Costa T; Cabrerizo Merino C; Rodríguez López F
An Esp Pediatr; 1981 Dec; 15(6):587-91. PubMed ID: 7337311
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. [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]
33. Partial trisomy 9q due to maternal 9q 17q translocation.
Nampoothiri S; Lakshman LR; Anilkumar A; Thampi MV
Indian Pediatr; 2008 Jul; 45(7):595-8. PubMed ID: 18695283
[TBL] [Abstract][Full Text] [Related]
34. [Inversion 8 and consecutive trisomy of region 8q22----qter].
Andrle M; Erlach A; Schweizer C
Wien Klin Wochenschr; 1987 Sep; 99(18):638-41. PubMed ID: 3687023
[TBL] [Abstract][Full Text] [Related]
35. De novo trisomy 22 due to an extra 22Q-chromosome.
Stoll C; Medeiros P; Pécheur H; Schnebelen A
Ann Genet; 1997; 40(4):217-21. PubMed ID: 9526616
[TBL] [Abstract][Full Text] [Related]
36. Towards mapping phenotypical traits in 18p- syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation.
Brenk CH; Prott EC; Trost D; Hoischen A; Walldorf C; Radlwimmer B; Wieczorek D; Propping P; Gillessen-Kaesbach G; Weber RG; Engels H
Eur J Hum Genet; 2007 Jan; 15(1):35-44. PubMed ID: 17024214
[TBL] [Abstract][Full Text] [Related]
37. "Essentially pure" partial trisomy (6)(p23-->pter) in two brothers due to maternal t(6;17)(p23;p13.3).
Röthlisberger B; Kotzot D; Gnehm HE; Schinzel A
Am J Med Genet; 1999 Aug; 85(4):389-94. PubMed ID: 10398266
[TBL] [Abstract][Full Text] [Related]
38. 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]
39. [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]
40. [Partial trisomy 18q].
Darnaude MT; López Pajares I; Delicado A; García Frias E
An Esp Pediatr; 1987 Jun; 26(6):460-2. PubMed ID: 3631780
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]