270 related articles for article (PubMed ID: 9032644)
1. At least nine cases of trisomy 11q23-->qter in one generation as a result of familial t(11;13) translocation.
Smeets D; van Ravenswaaij C; de Pater J; Gerssen-Schoorl K; Van Hemel J; Janssen G; Smits A
J Med Genet; 1997 Jan; 34(1):18-23. PubMed ID: 9032644
[TBL] [Abstract][Full Text] [Related]
2. A severely mentally and motor retarded girl with monosomy 3pter-->p25 and trisomy 8q24-->qter due to a familial reciprocal translocation t(3;8)(p25;q24).
Balci S; Aypar E; Beksaç MS; Bartsch O
Genet Couns; 2009; 20(2):125-32. PubMed ID: 19650409
[TBL] [Abstract][Full Text] [Related]
3. Partial trisomy 13q22-->qter and monosomy 18q21-->qter as a result of familial translocation.
Cekada S; Kilvain S; Brajenović-Milić B; Brecević L; Kirincić-Paucić E; Franulović J
Acta Paediatr; 1999 Jun; 88(6):675-8. PubMed ID: 10419257
[TBL] [Abstract][Full Text] [Related]
4. Partial trisomy 2p.
Pueschel SM; Scola PS; Mendoza T
J Ment Defic Res; 1987 Sep; 31 ( Pt 3)():293-8. PubMed ID: 3681957
[TBL] [Abstract][Full Text] [Related]
5. A rare case of trisomy 11q23.3-11q25 and trisomy 22q11.1-22q11.21.
Zou PS; Li HF; Chen LS; Ma M; Chen XH; Xue D; Cao DH
Genet Mol Res; 2016 May; 15(2):. PubMed ID: 27173335
[TBL] [Abstract][Full Text] [Related]
6. Genotype/phenotype analysis in a male patient with partial trisomy 4p and monosomy 20q due to maternal reciprocal translocation (4;20): A case report.
Wu D; Zhang H; Hou Q; Wang H; Wang T; Liao S
Mol Med Rep; 2017 Nov; 16(5):6222-6227. PubMed ID: 28901405
[TBL] [Abstract][Full Text] [Related]
7. Partial trisomy 6p from a de novo translocation (6;18) with variable mosaicism in different tissues.
Rudnik-Schöneborn S; Schubert R; Majewski F; Haverkamp F; Schwanitz G
Clin Genet; 1997 Aug; 52(2):126-9. PubMed ID: 9298749
[TBL] [Abstract][Full Text] [Related]
8. Autosomal reciprocal translocations and 13/14 translocations: a population study.
Nielsen J; Rasmussen K
Clin Genet; 1976 Sep; 10(3):161-77. PubMed ID: 786515
[TBL] [Abstract][Full Text] [Related]
9. Partial trisomy 8q. Two case reports with maternal translocation and inverted insertion: phenotype analyses and reflections on the risk.
Stengel-Rutkowski S; Lohse K; Herzog C; Apacik C; Couturier J; Albert A; Belohradsky B
Clin Genet; 1992 Oct; 42(4):178-85. PubMed ID: 1424241
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. The 2p partial trisomy syndrome. Duplication of region 2p23 leads to 2pter in two members of a t(2;7) translocation kindred.
Francke U; Jones KL
Am J Dis Child; 1976 Nov; 130(11):1244-9. PubMed ID: 984008
[TBL] [Abstract][Full Text] [Related]
12. Familial subtelomeric rearrangement of chromosomes 19 and 20: a new contribution to partial distal 19q trisomy.
Lenzini E; Drigo P; Redaelli S; Mammi I; Rosa-Rizzotto M; Dalprà L
Genet Test Mol Biomarkers; 2010 Oct; 14(5):695-701. PubMed ID: 20854099
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy 7p associated with familial 7p;22q translocation.
Larson LM; Wasdahl WA; Jalal SM
J Med Genet; 1977 Aug; 14(4):258-61. PubMed ID: 926137
[TBL] [Abstract][Full Text] [Related]
14. Partial trisomy 12q.
Zabel B; Baumann W
J Med Genet; 1981 Apr; 18(2):144-6. PubMed ID: 7241532
[TBL] [Abstract][Full Text] [Related]
15. A novel maternally-derived insertional translocation resulting in partial trisomy 4q13.2-q22.1 with complex translocation t(8;20) in a family with intellectual disability.
Assawamakin A; Wattanasirichaigoon D; Tocharoentanaphol C; Waeteekul S; Tansatit M; Thongnoppakhun W; Limwongse C
Am J Med Genet A; 2012 Apr; 158A(4):901-8. PubMed ID: 22419381
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].
Grasshoff U; Singer S; Liehr T; Starke H; Fode B; Schöning M; Dufke A
Cytogenet Genome Res; 2003; 103(1-2):17-23. PubMed ID: 15004458
[TBL] [Abstract][Full Text] [Related]
18. Risks of unbalanced progeny at amniocentesis to carriers of chromosome rearrangements: data from United States and Canadian laboratories.
Daniel A; Hook EB; Wulf G
Am J Med Genet; 1989 May; 33(1):14-53. PubMed ID: 2750783
[TBL] [Abstract][Full Text] [Related]
19. Reproductive possibilities for balanced translocation (14) carriers in families with partial trisomy of proximal 14q.
Valkova G; Stefanova M
J Med Genet; 1993 Jan; 30(1):73-5. PubMed ID: 8423613
[TBL] [Abstract][Full Text] [Related]
20. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
