236 related articles for article (PubMed ID: 6985016)
1. [Attenuated phenotype of trisomy 4p by translocation t(X;4)(p21.2;p13)].
Morichon-Delvallez N; Couturier J; Frison B
Ann Genet; 1982; 25(4):246-8. PubMed ID: 6985016
[TBL] [Abstract][Full Text] [Related]
2. "Pure" partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21).
de Almeida JC; Reis DF; Llerena JC; Pereira ET
Ann Genet; 1989; 32(3):181-3. PubMed ID: 2817779
[TBL] [Abstract][Full Text] [Related]
3. [Familial translocation t(4;22) (p11;p12) and trisomy 4p in 2 sisters].
Giovannelli G; Forabosco A; Dutrillaux B
Ann Genet; 1974 Jun; 17(2):119-24. PubMed ID: 4547939
[No Abstract] [Full Text] [Related]
4. [A new case of trisomy 5p].
Antonenko VG; Levina LIa; Chudnova VI
Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794
[TBL] [Abstract][Full Text] [Related]
5. Reduced phenotypic effect on partial trisomy 1q in a X/1 translocation.
Zuffardi O; Tiepolo L; Scappaticci S; Francesconi D; Bianchi C; di Natale D
Ann Genet; 1977 Sep; 20(3):191-94. PubMed ID: 304704
[TBL] [Abstract][Full Text] [Related]
6. Partial X chromosome trisomy with functional disomy of Xp due to failure of X inactivation.
Gustashaw KM; Zurcher V; Dickerman LH; Stallard R; Willard HF
Am J Med Genet; 1994 Oct; 53(1):39-45. PubMed ID: 7802034
[TBL] [Abstract][Full Text] [Related]
7. Combined trisomy 9 and Ullrich-Turner syndrome in a girl with a 46,X,der(9)t(X;9)(q12;q32) karyotype.
Canún S; Mutchinick O; Shaffer LG; Fernández C
Am J Med Genet; 1998 Nov; 80(3):199-203. PubMed ID: 9843037
[TBL] [Abstract][Full Text] [Related]
8. Mild phenotype and normal gonadal function in females with 4p trisomy due to unbalanced t(X;4)(p22.1;p14).
Petit P; Hilliker C; Van Leuven F; Fryns JP
Clin Genet; 1994 Oct; 46(4):304-8. PubMed ID: 7834896
[TBL] [Abstract][Full Text] [Related]
9. A second example of telomeric fusion 2 X chromosomes.
Fraisse J; Laurent C; Collard N; Biemont MC; Dutrillaux B
Ann Genet; 1975 Dec; 18(4):243-5. PubMed ID: 1083194
[TBL] [Abstract][Full Text] [Related]
10. [Familial chromosome translocation (1;5;15) as a cause of partial trisomy 1p].
Schürmann M; Wethling H; Niemeyer ML; Schwinger E
Klin Padiatr; 1987; 199(1):27-31. PubMed ID: 2435950
[TBL] [Abstract][Full Text] [Related]
11. [2 cases of partial trisomy 10p due to a paternal translocation t(10p;18)(p13;q23)].
Morić-Petrović S; Laća Z; Krajgher A; Milośevic J
Ann Genet; 1976 Sep; 19(3):195-7. PubMed ID: 1086628
[TBL] [Abstract][Full Text] [Related]
12. Follow-up of a patient with partial trisomy 9p and partial monosomy 8p; description of physical and psychosocial development.
Ausems MG; Van Spijker HG; Dijkhuis HJ; Swanenburg De Veye HF; Bijlsma JB
Genet Couns; 1996; 7(1):61-5. PubMed ID: 8652090
[TBL] [Abstract][Full Text] [Related]
13. [Trisomy 4p due to translocation t (4p--,22p+). Familial findings in 4 generations].
Forabosco A; Giovannelli G; Marzona L; Canè V
Minerva Pediatr; 1976 Apr; 28(12-3):743-51. PubMed ID: 995081
[No Abstract] [Full Text] [Related]
14. Mild expression of 3qter trisomy due to a de novo (X;3)(p22.3;q25.3) translocation.
Rivera H; Möller M; Arreola R; Cantu JM
Ann Genet; 1984; 27(2):112-4. PubMed ID: 6331787
[TBL] [Abstract][Full Text] [Related]
15. Trisomy 4p in a family with A t(4;15).
Hustinx WJ; Gabreëls JM; Kirkels VG; Korten JJ; Scheres JM; Joosten EM; Rutten FJ
Ann Genet; 1975 Mar; 18(1):13-9. PubMed ID: 1080034
[TBL] [Abstract][Full Text] [Related]
16. Trisomy 15q23----qter due to a de novo t(11;15)(q25;q23) and assignment of the critical segment.
García-Cruz D; García-Esquivel L; Rivera H; Vaca G; Rolón A; Cantú JM
Ann Genet; 1985; 28(3):193-6. PubMed ID: 3879157
[TBL] [Abstract][Full Text] [Related]
17. [A case of X/X translocation: t(X;X) (q26;p11)].
Wagenbichler P; Frisch H; Schnedl W
Klin Padiatr; 1975 Nov; 187(6):533-7. PubMed ID: 765610
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Brief clinical report: dup(4p15 leads to 4pter) in a 19-year-old woman resulting from a maternal 4;14 translocation.
Clark CE; Telfer MA; Cowell HR; Kalamchi A; Steg NL
Am J Med Genet; 1982 Jan; 11(1):37-42. PubMed ID: 7065001
[TBL] [Abstract][Full Text] [Related]
20. Trisomy 16pter to 16q12.1 and monosomy 22pter to 22q11.2 resulting from adjacent-2 segregation of a maternal complex chromosome rearrangement.
Xu J; Chernos J; Roland B
Am J Med Genet; 1997 Dec; 73(3):327-9. PubMed ID: 9415693
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]