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2. Der(22)t(11;22) resulting from a paternal de novo translocation, adjacent 1 segregation, and maternal heterodisomy of chromosome 22. Dawson AJ; Mears AJ; Chudley AE; Bech-Hansen T; McDermid H J Med Genet; 1996 Nov; 33(11):952-6. PubMed ID: 8950677 [TBL] [Abstract][Full Text] [Related]
3. Use of fluorescence in situ hybridization to confirm the interpretation of a balanced complex chromosome rearrangement ascertained through prenatal diagnosis. Wang H; McLaughlin M; Thompson C; Hunter AG Am J Med Genet; 1993 Jun; 46(5):559-62. PubMed ID: 8322821 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unbalanced karyotypes in sibs. Wieczorek D; Engels H; Viersbach R; Henke B; Schwanitz G; Passarge E J Med Genet; 1998 Jul; 35(7):545-53. PubMed ID: 9678698 [TBL] [Abstract][Full Text] [Related]
6. Partial trisomy 1p due to paternal t(1;9) translocation in a family with recurrent miscarriages. Demirhan O; Tastemir D Fertil Steril; 2006 Jul; 86(1):219.e15-9. PubMed ID: 16818035 [TBL] [Abstract][Full Text] [Related]
7. Maternal balanced translocation leading to partial duplication of 4q and partial deletion of 1p in a son: cytogenetic and FISH studies using band-specific painting probes generated by chromosome microdissection. Chen Z; Grebe TA; Guan XY; Notohamiprodjo M; Nutting PJ; Stone JF; Trent JM; Sandberg AA Am J Med Genet; 1997 Aug; 71(2):160-6. PubMed ID: 9217215 [TBL] [Abstract][Full Text] [Related]
8. Unbalanced translocation der(11)t(11;12)(q23;q13): a new recurrent cytogenetic aberration in myelodysplastic syndrome with a complex karyotype. Yamamoto K; Hato A; Minagawa K; Yakushijin K; Urahama N; Gomyo H; Sada A; Okamura A; Ito M; Matsui T Cancer Genet Cytogenet; 2004 Nov; 155(1):67-73. PubMed ID: 15527905 [TBL] [Abstract][Full Text] [Related]
9. The unbalanced offspring of the male carriers of the 11q;22q translocation: nondisjunction at meiosis II in a balanced spermatocyte. Simi P; Ceccarelli M; Barachini A; Floridia G; Zuffardi O Hum Genet; 1992 Feb; 88(4):482-3. PubMed ID: 1740326 [TBL] [Abstract][Full Text] [Related]
10. Not all chromosome imbalance resulting from the 11q;22q translocation is due to 3:1 segregation in first meiosis. Lockwood DH; Farrier A; Hecht F; Allanson J Hum Genet; 1989 Oct; 83(3):287-8. PubMed ID: 2793173 [TBL] [Abstract][Full Text] [Related]
11. Unusual mosaic karyotype resulting from adjacent 1 segregation of t(11;22): importance of performing skin fibroblast karyotype in patients with unexplained multiple congenital anomalies. Kulharya AS; Lovell CM; Flannery DB Am J Med Genet; 2002 Dec; 113(4):367-70. PubMed ID: 12457409 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. A small (sSMC) chromosome 22 due to a maternal translocation between chromosomes 8 and 22: a case report. Mundhofir FE; Kooper AJ; Winarni TI; Smits AP; Faradz SM; Hamel BC Genet Couns; 2010; 21(1):99-108. PubMed ID: 20420036 [TBL] [Abstract][Full Text] [Related]
14. Molecular cytogenetic characterization of a familial balanced reciprocal translocation t(11;18) (q13.3; q23) associated with pregnancy wastage. Liu JY; Wang XR; Zeng XL; Zhang CS; Hao S; Song YC Cytogenet Genome Res; 2003; 103(1-2):8-13. PubMed ID: 15004456 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Supernumerary chromosome marker Der(22)t(11;22) resulting from a maternal balanced translocation. Hou JW Chang Gung Med J; 2003 Jan; 26(1):48-52. PubMed ID: 12656309 [TBL] [Abstract][Full Text] [Related]
17. Trisomy 18q: 46,XX,13q+,t(13;18)(q32;q11) in a newborn associated with multiple congenital anomalies due to paternal reciprocal translocation, 46,XY,-13,+der(13),t(13;18)(q32;q11). Murthy DS; Patel ZM; Ambani LM Clin Genet; 1980 Oct; 18(4):233-8. PubMed ID: 7438504 [TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis of a familial complex chromosomal rearrangement involving chromosomes 5, 10, 16 and 18. Lee MH; Park SY; Kim YM; Kim JM; Han JY; Kim MY; Ryu HM Prenat Diagn; 2002 Feb; 22(2):102-4. PubMed ID: 11857612 [TBL] [Abstract][Full Text] [Related]
19. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype. Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518 [TBL] [Abstract][Full Text] [Related]
20. Confirmation of trisomy 22 in two cases using chromosome painting: comparison with t(11;22). Slater HR; Voullaire LE; Vaux CE; Bankier A; Pertile M; Choo KH Am J Med Genet; 1993 Jun; 46(4):434-7. PubMed ID: 8357017 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]