308 related articles for article (PubMed ID: 4787842)
1. Trisomy of the short arm of chromosome 8: association with translocation between chromosomes 8 and 22 46,XY,22-,t(8p22q) plus.
Rosenthal IM; Krmpotic E; Bocian M; Szego K
Clin Genet; 1973 Jun; 4(6):507-16. PubMed ID: 4787842
[No Abstract] [Full Text] [Related]
2. Partial trisomy of 13(pter to q12) due to 47,XY, + der(13),t(13;22)(q12;q13)mat.
Moedjono SJ; Sparkes RS
Hum Genet; 1979 Sep; 50(3):241-6. PubMed ID: 489007
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 12 in a mentally retarded boy and translocation (12;21) in his mother.
Hobolth N; Jacobsen P; Mikkelsen M
J Med Genet; 1974 Sep; 11(3):299-303. PubMed ID: 4139263
[TBL] [Abstract][Full Text] [Related]
4. Case report. Familial 4-22 translocation with partial trisomy for the short arm of chromosome 4 in two sibs.
Sartori A; Tenconi R; Baccichetti C; Pujatti G
Acta Paediatr Scand; 1974 Jul; 63(4):631-5. PubMed ID: 4850900
[No Abstract] [Full Text] [Related]
5. A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.
Short EM; Solitare GB; Breg WR
J Med Genet; 1972 Sep; 9(3):367-73. PubMed ID: 5079109
[No Abstract] [Full Text] [Related]
6. An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.
Jacobsen P; Hauge M; Henningsen K; Hobolth N; Mikkelsen M; Philip J
Hum Hered; 1973; 23(6):568-85. PubMed ID: 4134631
[No Abstract] [Full Text] [Related]
7. An extra small metacentric chromosome in association with multiple congenital abnormalities.
Finley WH; Finley SC; Monsky D
J Med Genet; 1971 Sep; 8(3):381-3. PubMed ID: 5097148
[No Abstract] [Full Text] [Related]
8. Partial trisomy 7p associated with familial 7p;22q translocation.
Larson LM; Wasdahl WA; Jalal SM
J Med Genet; 1977 Aug; 14(4):258-61. PubMed ID: 926137
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy of chromosome 11: a case report.
Falk RE; Carrel RE; Valente M; Crandall BF; Sparkes RS
Am J Ment Defic; 1973 Jan; 77(4):383-8. PubMed ID: 4706396
[No Abstract] [Full Text] [Related]
10. Tertiary trisomy in a human kindred containing an E/G translocation.
Macintyre MN; Walden DB; Hempel JM
Am J Hum Genet; 1971 Sep; 23(5):431-41. PubMed ID: 5092595
[No Abstract] [Full Text] [Related]
11. Quinacrine mustard fluorescence of human chromosomes: characterization of unusual translocations.
Francke U
Am J Hum Genet; 1972 Mar; 24(2):189-213. PubMed ID: 5016511
[No Abstract] [Full Text] [Related]
12. Study of a patient with apparent monosomy 21 owing to translocation: 45,XX,21-,t(18q+).
Wyandt HE; Hecht F; Lovrien EW; Stewart RE
Cytogenetics; 1971; 10(6):413-26. PubMed ID: 5146418
[No Abstract] [Full Text] [Related]
13. Identification of chromosomal abnormalities by quinacrine-staining technique in patients with normal karyotypes by conventional analysis.
del Solar C; Uchida IA
J Pediatr; 1974 Apr; 84(4):534-8. PubMed ID: 4134885
[No Abstract] [Full Text] [Related]
14. Transmission of a translocation t(Cp+; Dq-) through three generations; including an example of probable trisomy for the short arm of the C group chromosome No. 9.
Butler LJ; Eades SM; France NE
Ann Genet; 1969 Mar; 12(1):15-27. PubMed ID: 5306708
[No Abstract] [Full Text] [Related]
15. Unbalanced X-autosomal translocation with inactivation of the normal X chromosome.
Mikkelsen M; Dahl G
Cytogenet Cell Genet; 1973; 12(5):357-66. PubMed ID: 4131091
[No Abstract] [Full Text] [Related]
16. Partial trisomy 8 (8q24) and the trisomy-8 syndrome.
Sánchez O; Yunis JJ
Humangenetik; 1974; 23(4):297-303. PubMed ID: 4420964
[No Abstract] [Full Text] [Related]
17. Pure partial trisomy for long arm of chromosome 9.
Faed M; Robertson J; Brown S; Smail PJ; Muckhart RD
J Med Genet; 1976 Jun; 13(3):239-42. PubMed ID: 933125
[TBL] [Abstract][Full Text] [Related]
18. Familial translocation involving chromosomes 6, 14 and 20, identified by quinacrine fluorescence.
Allderdice PW; Miller OJ; Miller DA; Breg WR; Gendel E; Zelson C
Humangenetik; 1971; 13(3):205-9. PubMed ID: 5114675
[No Abstract] [Full Text] [Related]
19. Three non-mongoloid patients of similar phenotype with an extra G-like chromosome.
Gustavson KH; Hitrec V; Santesson B
Clin Genet; 1972; 3(2):135-46. PubMed ID: 5054315
[No Abstract] [Full Text] [Related]
20. A partial D-trisomy-normal mosaic female.
Webb GC; Garson M; Robson MK; Pitt DB
J Med Genet; 1971 Dec; 8(4):522-7. PubMed ID: 5149538
[No Abstract] [Full Text] [Related]
[Next] [New Search]