137 related articles for article (PubMed ID: 1536164)
21. Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study.
Hsu LY; Yu MT; Richkind KE; Van Dyke DL; Crandall BF; Saxe DF; Khodr GS; Mennuti M; Stetten G; Miller WA; Priest JH
Prenat Diagn; 1996 Jan; 16(1):1-28. PubMed ID: 8821848
[TBL] [Abstract][Full Text] [Related]
22. Identification of a subtle chromosomal translocation in a family with recurrent miscarriages and a child with multiple congenital anomalies. A case report.
Shaffer LG; Spikes AS; Macha M; Dunn R
J Reprod Med; 1996 May; 41(5):367-71. PubMed ID: 8725766
[TBL] [Abstract][Full Text] [Related]
23. Late separating D/D fusions in subjects with "balanced" translocation.
Méhes K; Bajnóczky K; Bühler EM; Kosztolanyi G
Ann Genet; 1991; 34(1):19-21. PubMed ID: 1952785
[TBL] [Abstract][Full Text] [Related]
24. Trisomy first, translocation second, uniparental disomy and partial trisomy third: a new mechanism for complex chromosomal aneuploidy.
Schinzel A; Kotzot D; Brecevic L; Robinson WP; Dutly F; Dauwerse H; Binkert F; Baumer A; Ausserer B
Eur J Hum Genet; 1997; 5(5):308-14. PubMed ID: 9412788
[TBL] [Abstract][Full Text] [Related]
25. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Highly abnormal cleavage divisions in preimplantation embryos from translocation carriers.
Iwarsson E; Malmgren H; Inzunza J; Ahrlund-Richter L; Sjöblom P; Rosenlund B; Fridström M; Hovatta O; Nordenskjöld M; Blennow E
Prenat Diagn; 2000 Dec; 20(13):1038-47. PubMed ID: 11180227
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Duplication 7p in a family with t(7;11): association with anomalies of the anterior cranial base.
Odell JM; Siebert JR; Bradley C; Salk D
Am J Med Genet; 1987 Jul; 27(3):687-92. PubMed ID: 3631140
[TBL] [Abstract][Full Text] [Related]
30. A case of mosaicism involving an unstable 13/14 Robertsonian translocation.
Wells S; Gregson N; Porter RJ
Prenat Diagn; 1991 Nov; 11(11):875-80. PubMed ID: 1754558
[TBL] [Abstract][Full Text] [Related]
31. Cytogenetic studies in 30 patients with Burkitt's lymphoma or L3 acute lymphoblastic leukemia with special reference to additional chromosome abnormalities.
Lai JL; Fenaux P; Zandecki M; Nelken B; Huart JJ; Deminatti M
Ann Genet; 1989; 32(1):26-32. PubMed ID: 2751244
[TBL] [Abstract][Full Text] [Related]
32. [Results of chromosomal studies in 270 couples with reproductive problems].
Castillo S; Sanz P; Astete C; Daher V; Tobella L; Salazar S
Rev Chil Obstet Ginecol; 1991; 56(1):38-42. PubMed ID: 1844599
[TBL] [Abstract][Full Text] [Related]
33. Mosaicism for del(17)(p11.2p11.2) underlying the Smith-Magenis syndrome.
Juyal RC; Kuwano A; Kondo I; Zara F; Baldini A; Patel PI
Am J Med Genet; 1996 Dec; 66(2):193-6. PubMed ID: 8958329
[TBL] [Abstract][Full Text] [Related]
34. Balanced reciprocal translocation mosaicism: how frequent?
Opheim KE; Brittingham A; Chapman D; Norwood TH
Am J Med Genet; 1995 Jul; 57(4):601-4. PubMed ID: 7573137
[TBL] [Abstract][Full Text] [Related]
35. Familial ring (19) chromosome mosaicism: case report and review.
Flejter WL; Finlinson D; Root S; Nguyen W; Brothman AR; Viskochil D
Am J Med Genet; 1996 Dec; 66(3):276-80. PubMed ID: 8985487
[TBL] [Abstract][Full Text] [Related]
36. Noninactivation of a portion of Xq28 in a balanced X-autosome translocation.
Du Sart D; Kalitsis P; Schmidt M
Am J Med Genet; 1992 Jan; 42(2):156-60. PubMed ID: 1733163
[TBL] [Abstract][Full Text] [Related]
37. Detection of an unbalanced translocation (4;14) in a mildly retarded father and son by flow cytometry.
Cooke A; Tolmie JL; Colgan JM; Greig CM; Connor JM
Hum Genet; 1989 Aug; 83(1):83-7. PubMed ID: 2570022
[TBL] [Abstract][Full Text] [Related]
38. Clinical diagnosis of partial duplication 7q.
Bartsch O; Kalbe U; Ngo TK; Lettau R; Schwinger E
Am J Med Genet; 1990 Oct; 37(2):254-7. PubMed ID: 2248294
[TBL] [Abstract][Full Text] [Related]
39. Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult.
Papenhausen PR; Mueller OT; Johnson VP; Sutcliffe M; Diamond TM; Kousseff BG
Am J Med Genet; 1995 Nov; 59(3):271-5. PubMed ID: 8599348
[TBL] [Abstract][Full Text] [Related]
40. Unusual de novo t(13;15)(q12.1;p13) translocation leading to complex mosaicism including jumping translocation.
Petit P; Devriendt K; Vermeesch JR; De Cock P; Fryns JP
Ann Genet; 1998; 41(1):22-6. PubMed ID: 9599647
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
