158 related articles for article (PubMed ID: 4141377)
1. Banding identification of partial trisomy 15 and of 8/21 translocation.
Wurster-Hill DH; Hoefnagel D
J Ment Defic Res; 1974 Jun; 18(2):139-44. PubMed ID: 4141377
[No Abstract] [Full Text] [Related]
2. 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]
3. Inherited partial duplication of chromosome No. 15.
Fujimoto A; Towner JW; Ebbin AJ; Kahlstrom EJ; Wilson MG
J Med Genet; 1974 Sep; 11(3):287-91. PubMed ID: 4139262
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. Partial trisomy 4q and partial monosomy 18q as a consequence of a paternal balanced translocation t(4qminus; 18qplus).
Fonatsch C; Flatz SD
Humangenetik; 1974; 25(3):227-33. PubMed ID: 4141336
[No Abstract] [Full Text] [Related]
8. A possible case of partial trisomy for chromosome 22: further evidence from Giemsa banding studies.
Sands ME
J Ment Defic Res; 1974 Dec; 18(4):327-30. PubMed ID: 4142949
[No Abstract] [Full Text] [Related]
9. Possible complex translocation t(9;14;13) (q12;pl?;Q31) in mother of a child with 9-p trisomy syndrome.
Fujita H; Abe T; Yamamoto K; Furuyama J
Humangenetik; 1974; 25(2):83-92. PubMed ID: 4140843
[No Abstract] [Full Text] [Related]
10. Partial trisomy 11q as the result of sporadic translocation.
Lurie IW; Lazjuk GI; Usova YI; Gurevich DB
Hum Genet; 1979 Sep; 51(1):63-6. PubMed ID: 500093
[TBL] [Abstract][Full Text] [Related]
11. Four cases of 9p trisomy resulting from a balanced familial translocation (9:15) (q13;q11). Clinical picture and cytogenetic findings.
Zaremba J; Zdzienicka E; Glogowska I; Abramowicz T; Taracha B
J Ment Defic Res; 1974 Jun; 18(2):153-90. PubMed ID: 4141378
[No Abstract] [Full Text] [Related]
12. Partial trisomy 8: further observation of a familial C-G translocation chromosome identified by the Q-staining methods.
Yanagisawa S
J Ment Defic Res; 1973 Mar; 17(1):28-32. PubMed ID: 4137098
[No Abstract] [Full Text] [Related]
13. Familial C-G translocation in three relatives associated with severe mental retardation, short stature, unusual dermatoglyphics and other malformations.
Yanagisawa S; Hiraoka K
J Ment Defic Res; 1971 Jun; 15(2):136-46. PubMed ID: 5559234
[No Abstract] [Full Text] [Related]
14. Trisomy 9p resulting from maternal 9/21 translocation.
Sŭbrt I; Blehová B; Pallová B
Hum Genet; 1976 May; 32(2):217-20. PubMed ID: 944684
[TBL] [Abstract][Full Text] [Related]
15. A case of trisomy 9p in a family with translocation 9/15.
Balícek P; Zizka J; Lichý J
Humangenetik; 1975; 27(4):353-8. PubMed ID: 1150257
[No Abstract] [Full Text] [Related]
16. 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]
17. 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]
18. Trisomy 9p in a girl whose mother has a translocation t(9;20)(q12;p13).
Stoll C; Levy JM; Gardea A
Humangenetik; 1975; 27(3):269-74. PubMed ID: 1150249
[No Abstract] [Full Text] [Related]
19. Partial trisomy 11 in a child resulting from a complex maternal rearrangement of chromosomes 11, 12 and 13.
Sanchez O; Yunis JJ; Escobar JI
Humangenetik; 1974 Apr; 22(1):59-65. PubMed ID: 4134840
[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]
