120 related articles for article (PubMed ID: 7307309)
1. Partial trisomy 3q due to a de novo translocation t(X;3) (p21;q12).
Oorthuys JW; Slater RM; Barrowclough H; de Kleine MJ
Clin Genet; 1981 Aug; 20(2):130-4. PubMed ID: 7307309
[TBL] [Abstract][Full Text] [Related]
2. Partial trisomy of chromosome 3 (3q12 leads to qter) owing to 3q/18p translocation. A trisomy 3q syndrome.
Salazar D; Rosenfeld W; Verma RS; Jhaveri RC; Dosik H
Am J Dis Child; 1979 Oct; 133(10):1006-8. PubMed ID: 495588
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 3q in a newborn female.
De Marchi M; Zuffardi O; Carozzi F; Schmid W; Carbonara AO
Ric Clin Lab; 1977; 7(3):225-32. PubMed ID: 605339
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Hereditary 3;6 translocation : three cases of multiple malformations with partial trisomy 6p21 leads to pter.
Pagano L; Fioretti G; Vetrella M; Risolo E; Casullo C; Celona A; Renda S; Rinaldi A; Ventruto V
Ann Genet; 1980; 23(3):173-5. PubMed ID: 6968535
[TBL] [Abstract][Full Text] [Related]
6. Partial trisomy 14 (q23 leads to qter) via segregation of a 14/X translocation.
Cohen MM; Charrow J; Balkin NE; Harris CJ
Am J Hum Genet; 1983 Jul; 35(4):635-44. PubMed ID: 6881140
[TBL] [Abstract][Full Text] [Related]
7. Partial 3q trisomy due to an unbalanced 3/10 translocation.
Blumberg B; Moore R; Mohandas T
Am J Med Genet; 1980; 7(3):335-9. PubMed ID: 7468658
[TBL] [Abstract][Full Text] [Related]
8. [Partial trisomy of the long arm of chromosome 2 by malsegregation of a maternal translocation t(2;7)(q321;p22)].
Siffroi JP; Romani F; Viguié F; Lejeune C
Ann Genet; 1984; 27(4):241-4. PubMed ID: 6335372
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 46, XY, t(3;22) (p2;q13) resulting in partial trisomy for the short arm of chromosome 3.
Surana RB; Braudo ME; Conen PE; Slade RH
Clin Genet; 1977 Mar; 11(3):201-6. PubMed ID: 837571
[No Abstract] [Full Text] [Related]
11. A child with partial trisomy of chromosome 17 and partial monosomy of chromosome 3: 46,XY,der(3),t(3;17)(p25;q23).
Shawe DJ; Fear C; Appleyard WJ
J Med Genet; 1983 Oct; 20(5):383-5. PubMed ID: 6196484
[TBL] [Abstract][Full Text] [Related]
12. [Familial translocation 3/22 MAT with partial trisomy 3q (author's transl)].
Schwanitz G; Schmid RD; Grosse G; Grahn-Liebe E
J Genet Hum; 1977 Jun; 25(2):141-50. PubMed ID: 556338
[TBL] [Abstract][Full Text] [Related]
13. A newborn child with karyotype 47,XX,+der(12 (12pter leads to 12q12::9q24 leads to 8qter),t(8;12) (q24;q12) pat.
Nielsen H; Vetner M; Holm V; Askjaer S; Reske-Nielsen E
Hum Genet; 1977 Mar; 35(3):357-62. PubMed ID: 844879
[No Abstract] [Full Text] [Related]
14. Phenotype of partial trisomy 8 (p21 leads to qter) in two unrelated patients with de novo translocation.
Sachs ES; van Waveren G
J Med Genet; 1981 Jun; 18(3):204-8. PubMed ID: 7241543
[TBL] [Abstract][Full Text] [Related]
15. 'Pure' partial trisomy 2q in a male owing to malsegregation of a maternal translocation t(X;2)(p22.3;q32.1).
Plessis G; Couturier J; Turleau C; Despoisses S; Delavenne J
J Med Genet; 1985 Feb; 22(1):70-3. PubMed ID: 3981584
[TBL] [Abstract][Full Text] [Related]
16. [Partial "de novo" trisomy 10q (author's transl)].
Berger R; Derre J; Murawsky M; Amiel-Tison C
J Genet Hum; 1976 Dec; 24(4):261-9. PubMed ID: 1022850
[TBL] [Abstract][Full Text] [Related]
17. Partial trisomy 13 as a result of de novo (6p;13q) translocation.
Jones LA; Taysi K; Strauss AW; Hartmann AF
Hum Genet; 1979 Apr; 48(2):245-9. PubMed ID: 457146
[TBL] [Abstract][Full Text] [Related]
18. Familial transmission of a 3q;22p translocation, with partial trisomy of chromosome 3 in the propositus.
Sod R; Giorgiutti E; Matayoshi T; de Kohan G; Munoz E
J Genet Hum; 1978 Jun; 26(2):173-6. PubMed ID: 670944
[TBL] [Abstract][Full Text] [Related]
19. Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.
Verma RS; Dosik H; Wexler IB
J Genet Hum; 1977 Dec; 25(4):295-301. PubMed ID: 599332
[TBL] [Abstract][Full Text] [Related]
20. Partial trisomy of 11 and 22 due to familial translocation t(11;22)(q23;q11), inherited in three generations.
Nakai H; Yamamoto Y; Kuroki Y
Hum Genet; 1979 Oct; 51(3):349-55. PubMed ID: 511169
[No Abstract] [Full Text] [Related]
[Next] [New Search]