176 related articles for article (PubMed ID: 5518460)
21. Translocation, t(4qminus;13qplus), in three generations resulting in partial trisomy of the long arm of chromosome 4 in the fourth generation.
Schrott HG; Sakaguchi S; Francke U; Luzzatti L; Fialkow PJ
J Med Genet; 1974 Jun; 11(2):201-5. PubMed ID: 4135220
[TBL] [Abstract][Full Text] [Related]
22. A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.
Watt JL; Olson IA; Johnston AW; Ross HS; Couzin DA; Stephen GS
J Med Genet; 1985 Aug; 22(4):283-7. PubMed ID: 4045954
[TBL] [Abstract][Full Text] [Related]
23. Familial balanced insertion (5;10) and monosomy and trisomy (10) (q24.2----q25.3).
van de Vooren MJ; Planteydt HT; Hagemeijer A; Peters-Slough MF; Timmerman MJ
Clin Genet; 1984 Jan; 25(1):52-8. PubMed ID: 6705241
[TBL] [Abstract][Full Text] [Related]
24. An extra small metacentric chromosome in a mentally retarded boy.
Ishmael J; Laurence KM
J Med Genet; 1968 Dec; 5(4):335-40. PubMed ID: 5713650
[No Abstract] [Full Text] [Related]
25. [Clinical and cytogenetic findings in a rare autosomal aberrations].
Tolksdorf M
Monatsschr Kinderheilkd (1902); 1970 Jun; 118(6):308-13. PubMed ID: 5523669
[No Abstract] [Full Text] [Related]
26. Chromosome banding patterns in an infant with 13q minus syndrome.
Ikeuchi T; Sonta S; Sasaki M; Hujita M; Tsunematsu K
Humangenetik; 1974 Mar; 21(4):309-14. PubMed ID: 4134627
[No Abstract] [Full Text] [Related]
27. Family chromosome studies.
Hecht F
J Pediatr; 1971 Apr; 78(4):735-6. PubMed ID: 5547838
[No Abstract] [Full Text] [Related]
28. [Abnormal C group chromosome in several members of the same family].
Emerit I; Vernant P
Humangenetik; 1968; 6(4):326-34. PubMed ID: 5713618
[No Abstract] [Full Text] [Related]
29. 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]
30. 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]
31. Short arm deletion of chromosome 14.
Emerit I; Noel B; Thiriet M; Loubon M; Quack B
Humangenetik; 1972; 15(1):33-8. PubMed ID: 5046906
[No Abstract] [Full Text] [Related]
32. Clinical, cytogenetic and autoradiographic studies in 10 cases with rare chromosome disorders. I. Cases 1 and 2.
Moore MK; Engel E
Ann Genet; 1969 Dec; 12(4):265-9. PubMed ID: 5309420
[No Abstract] [Full Text] [Related]
33. An inherited 1;G translocation.
Ebbin AJ; Wilson MG; Towner JW; Forsman I
J Med Genet; 1971 Dec; 8(4):536-9. PubMed ID: 5149540
[No Abstract] [Full Text] [Related]
34. Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4.
Van der Linden AG; Pearson PL; Van de Kamp JJ
Cytogenet Cell Genet; 1975; 14(2):126-39. PubMed ID: 1149493
[TBL] [Abstract][Full Text] [Related]
35. Pericentric enversion of chromosome no. 13 in a large family leading to duplication deficiency causing congenital malformations in three individuals.
Hauksdóttir H; Halldórsson S; Jensson O; Mikkelsen M; McDermott A
J Med Genet; 1972 Dec; 9(4):413-21. PubMed ID: 4646548
[No Abstract] [Full Text] [Related]
36. Presumed disturbance of a nucleolus organizer in man: chromosome 13qs and monosomy 15 mosaicism.
Hoehn H; Reinwein H
Humangenetik; 1971; 12(1):50-5. PubMed ID: 5556919
[No Abstract] [Full Text] [Related]
37. Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4.
Wilson MG; Towner JW; Negus LD
J Med Genet; 1970 Jun; 7(2):164-70. PubMed ID: 5519605
[No Abstract] [Full Text] [Related]
38. Ring chromosome 6 in a malformed boy.
Salamanca-Gonez F; Nava S; Armendares S
Clin Genet; 1975 Nov; 8(5):370-5. PubMed ID: 1204234
[TBL] [Abstract][Full Text] [Related]
39. Pericentric inversion of chromosome 11 in one of two similar retarded brothers.
Einfeld SL; Smith A
J Med Genet; 1982 Aug; 19(4):312. PubMed ID: 7120323
[No Abstract] [Full Text] [Related]
40. A complex four-break rearrangement between chromosomes 4 and 13 resulting in a recombinant chromosome 4.
Andersen O; Lundsteen C; Niebuhr E
Cytogenet Cell Genet; 1981; 30(1):3-10. PubMed ID: 7261680
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
