108 related articles for article (PubMed ID: 7985981)
21. Pediatric leukemia/lymphoma with t(8;14)(q24;q11).
Lange BJ; Raimondi SC; Heerema N; Nowell PC; Minowada J; Steinherz PE; Arenson EB; O'Connor R; Santoli D
Leukemia; 1992 Jul; 6(7):613-8. PubMed ID: 1385638
[TBL] [Abstract][Full Text] [Related]
22. [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]
23. [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]
24. Familial tiny 9p/20p translocation: 9p24. The critical segment for monosomy 9p syndrome.
Hoo JJ; Fischer A; Fuhrmann W
Ann Genet; 1982; 25(4):249-52. PubMed ID: 6985017
[TBL] [Abstract][Full Text] [Related]
25. [Correlation of amplification of chromosome 1 with histologic typing of thymic epithelial tumors].
Ma YQ; Zhang C; Cui WL; Gulinaer A; Zhang W; Wang J
Zhonghua Bing Li Xue Za Zhi; 2011 Dec; 40(12):820-4. PubMed ID: 22336207
[TBL] [Abstract][Full Text] [Related]
26. Apparent Smith-Lemli-Opitz syndrome and Miller-Dieker syndrome in a family with segregating translocation t(7;17)(q34;p13.1).
Berry R; Wilson H; Robinson J; Sandlin C; Tyson W; Campbell J; Porreco R; Manchester D
Am J Med Genet; 1989 Nov; 34(3):358-65. PubMed ID: 2596525
[TBL] [Abstract][Full Text] [Related]
27. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases.
Batista DA; Pai GS; Stetten G
Am J Med Genet; 1994 Nov; 53(3):255-63. PubMed ID: 7856662
[TBL] [Abstract][Full Text] [Related]
28. A case of myelodysplastic syndrome with erythroid hypoplasia associated with a familial translocation t(3;14)(p21.1;q24.1).
Dinçol G; Oztürk S; Palanduz S; Tutkan G; Yildirim N; Ayer M; Güvenç S
Am J Hematol; 2006 Nov; 81(11):883-7. PubMed ID: 16888788
[TBL] [Abstract][Full Text] [Related]
29. Giant hypertrophy of the thymus in three siblings.
Slowikowski J; Kubrakiewicz Z; Zieliński S
Pol Med J; 1968; 7(3):634-7. PubMed ID: 5669703
[No Abstract] [Full Text] [Related]
30. Complex chromosome rearrangements and congenital anomalies.
Kousseff BG; Nichols P; Essig YP; Miller K; Weiss A; Tedesco TA
Am J Med Genet; 1987 Apr; 26(4):771-82. PubMed ID: 3591822
[TBL] [Abstract][Full Text] [Related]
31. Transmission of ring 14 chromosome from mother to two sons.
Matalon R; Supple P; Wyandt H; Rosenthal IM
Am J Med Genet; 1990 Aug; 36(4):381-5. PubMed ID: 2202211
[TBL] [Abstract][Full Text] [Related]
32. [Dominant epidermolysis bullosa dystrophica of Cockayne-Touraine. Presentation of a familial case and cytogenetic investigation].
Amerio P; Pallotta R; Di Donato D; Dalprà L
G Ital Dermatol Venereol; 1988 Sep; 123(9):417-20. PubMed ID: 3243581
[No Abstract] [Full Text] [Related]
33. Clusters of chromosomal imbalances in thymic epithelial tumours are associated with the WHO classification and the staging system according to Masaoka.
Penzel R; Hoegel J; Schmitz W; Blaeker H; Morresi-Hauf A; Aulmann S; Hecker E; Mechtersheimer G; Otto HF; Rieker RJ
Int J Cancer; 2003 Jul; 105(4):494-8. PubMed ID: 12712440
[TBL] [Abstract][Full Text] [Related]
34. [Clinical anatomical contribution on 3 cases of thymoma].
Gandola L
Radiol Med; 1980 Mar; 66(3):152-4. PubMed ID: 7455226
[No Abstract] [Full Text] [Related]
35. Duplication 16q12----qter arising from 3:1 segregation in a 46,XX,t(13;16) (q12;q12) mother.
Pérez-Castillo A; Martin-Lucas MA; Abrisqueta JA
Ann Genet; 1990; 33(2):121-3. PubMed ID: 2241087
[TBL] [Abstract][Full Text] [Related]
36. Need for search for cryptic translocation in parents with several children affected with MCA: report of a cryptic translocation (10;14) detected by FISH.
Delneste D; Vamos E; Pierquin G; Hayez-Delatte F; Van Regemorter N
Genet Couns; 1998; 9(2):97-102. PubMed ID: 9664205
[TBL] [Abstract][Full Text] [Related]
37. Monosomy 11q: report of two familial cases and review of the literature.
Hustinx R; Verloes A; Grattagliano B; Herens C; Jamar M; Soyeur D; Schaaps JP; Koulischer L
Am J Med Genet; 1993 Sep; 47(3):312-7. PubMed ID: 8135272
[TBL] [Abstract][Full Text] [Related]
38. Deletion (6)(p22p25) is a recurrent anomaly of thymoma: report of a second case and review of the literature.
Herens C; Radermecker M; Servais A; Quatresooz P; Jardon-Jeghers C; Bours V; de Leval L
Cancer Genet Cytogenet; 2003 Oct; 146(1):66-9. PubMed ID: 14499698
[TBL] [Abstract][Full Text] [Related]
39. Ring chromosome 6 as the only change in a thymoma.
Dal Cin P; De Wolf-Peeters C; Aly MS; Deneffe G; Van Mieghem W; Van Den Berghe H
Genes Chromosomes Cancer; 1993 Apr; 6(4):243-4. PubMed ID: 7685629
[No Abstract] [Full Text] [Related]
40. Two cases of partial trisomy 10q syndrome due to a familial 10;20 translocation.
Tüysüz B; Hacihanefioglu S; Silahtaroglu A; Yilmaz S; Deviren A; Cenani A
Genet Couns; 2000; 11(4):355-61. PubMed ID: 11140413
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]