125 related articles for article (PubMed ID: 1605261)
1. Trisomy 16p in a liveborn offspring due to maternal translocation t(16;21)(q11;p11) and review of the literature.
Léonard C; Huret JL; Imbert MC; Lebouc Y; Selva J; Boulley AM
Am J Med Genet; 1992 Jun; 43(3):621-5. PubMed ID: 1605261
[TBL] [Abstract][Full Text] [Related]
2. Trisomy 16p in a liveborn infant and review of trisomy 16p.
O'Connor TA; Higgins RR
Am J Med Genet; 1992 Feb; 42(3):316-9. PubMed ID: 1536169
[TBL] [Abstract][Full Text] [Related]
3. Reciprocal translocations and full trisomy (trisomy 18 and trisomy 21) in the offspring.
Fryns JP; Kleczkowska A; Moerman P; Van den Berghe H
Ann Genet; 1986; 29(4):272-4. PubMed ID: 3495232
[TBL] [Abstract][Full Text] [Related]
4. Partial duplication 16p resulting from a 3:1 segregation of a maternal reciprocal translocation.
Mori MA; Gomar JL; Diaz de Bustamante A; Ananias A; Pinel I; Martinez-Frias ML
Am J Med Genet; 1987 Jan; 26(1):203-6. PubMed ID: 3812563
[TBL] [Abstract][Full Text] [Related]
5. Trisomy for the short arm of chromosome 10. Report of a new case resulting from segregation of a maternal balanced translocation t(10qter----q11::14p11----qter).
Delaroche I; Bruni L; Giannotti A; Giampaolo R; Aebischer ML
Helv Paediatr Acta; 1984 May; 39(2):161-6. PubMed ID: 6543839
[TBL] [Abstract][Full Text] [Related]
6. Trisomy 12p due to an adjacent 1 segregation of a maternal reciprocal translocation t(12;18) (p11;q23).
Tenconi R; Giorgi PL; Tarantino E; Formica A
Ann Genet; 1978 Dec; 21(4):229-33. PubMed ID: 314261
[TBL] [Abstract][Full Text] [Related]
7. Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13.
de Ravel T; Aerssens P; Vermeesch JR; Fryns JP
Eur J Med Genet; 2005; 48(3):355-9. PubMed ID: 16179232
[TBL] [Abstract][Full Text] [Related]
8. Atypical 18p- syndrome associated with partial trisomy 16p in a chromosomally unbalanced child of consanguineous parents with an identical balanced translocation.
Kupchik GS; Barrett SK; Babu A; Charria-Ortiz G; Velinov M; Macera MJ
Eur J Med Genet; 2005; 48(1):57-65. PubMed ID: 15953407
[TBL] [Abstract][Full Text] [Related]
9. Trisomy 20p: case report and genetic review.
Lurie IW; Rumyantseva NV; Zaletajev DV; Gurevich DB; Korotkova IA
J Genet Hum; 1985 Jan; 33(1):67-75. PubMed ID: 3981145
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Trisomy 14 mosaicism with t(14;15)(q11;p11) in offspring of a balanced translocation carrier mother.
Fujimoto A; Lin MS; Korula SR; Wilson MG
Am J Med Genet; 1985 Oct; 22(2):333-42. PubMed ID: 4050866
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberration.
Eggermann T; Kolin-Gerresheim I; Gerresheim F; Schwanitz G
Ann Genet; 1998; 41(4):205-8. PubMed ID: 9881183
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy of the distal part of 10q: a report of two Egyptian cases.
Aglan MS; Kamel AK; Helmy NA
Genet Couns; 2008; 19(2):199-209. PubMed ID: 18618995
[TBL] [Abstract][Full Text] [Related]
15. Second meiotic nondisjunction of the rearranged chromosome in a familial reciprocal 5/13 translocation.
Masuno M; Cholsong Y; Kuwahara T; Shimizu N; Yamaguchi S; Kawabata I; Tamaya T; Morishita Y; Yoshimi N; Orii T
Am J Med Genet; 1991 Oct; 41(1):32-4. PubMed ID: 1951460
[TBL] [Abstract][Full Text] [Related]
16. Duplication of distal 22q.
Abeliovich D; Maor E; Bashan N; Carmi R
Am J Med Genet; 1989 Mar; 32(3):346-9. PubMed ID: 2729354
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. [Familial translocation t (16;19) (q24;q11) and birth of a girl with a trisomy 18].
Stoll C; Messer J
Ann Pediatr (Paris); 1979 Jan; 26(1):38-40. PubMed ID: 16106870
[No Abstract] [Full Text] [Related]
19. Tertiary trisomy of 10p15.pter and 14pter.ql3 due to maternal translocation t(10;14)(p15;q13).
Cetin Z; Mihci E; Keser I; Luleci G
Genet Couns; 2012; 23(2):207-14. PubMed ID: 22876579
[TBL] [Abstract][Full Text] [Related]
20. Interchange trisomy 21 by t(1;21)(p22;q22)mat.
Dominguez MG; Rivera H; Vasquez AI; Hernández-Zaragoza G; Rivas F
Genet Couns; 2001; 12(4):363-7. PubMed ID: 11837606
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]