397 related articles for article (PubMed ID: 9678708)
1. Two cases of partial trisomy 8p and partial monosomy 21q in a family with a reciprocal translocation (8;21)(p21.1;q22.3).
Plomp AS; Engelen JJ; Albrechts JC; de Die-Smulders CE; Hamers AJ
J Med Genet; 1998 Jul; 35(7):604-8. PubMed ID: 9678708
[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. Variable expression of phenotype in offspring with partial monosomy 7q and partial trisomy 8p in a family with a rcp (7;8)(134;p12) translocation.
Frints SG; Moerman P; Fryns JP
Genet Couns; 1996; 7(4):313-9. PubMed ID: 8985736
[TBL] [Abstract][Full Text] [Related]
4. Unbalanced karyotype with normal phenotype in a family with translocation (8;13)(p21;q22).
Bröcker-Vriends AH; van de Kamp JJ; Geraedts JP; Bos SE; Nijenhuis TA
Clin Genet; 1985 May; 27(5):487-95. PubMed ID: 4006274
[TBL] [Abstract][Full Text] [Related]
5. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
8. [Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].
Xiao B; Zhang JM; Ji X; Jiang WT; Hu J; Tao J
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):247-50. PubMed ID: 21644216
[TBL] [Abstract][Full Text] [Related]
9. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients.
Szabó GP; Knegt AC; Ujfalusi A; Balogh E; Szabó T; Oláh É
Am J Med Genet A; 2012 Apr; 158A(4):869-76. PubMed ID: 22407767
[TBL] [Abstract][Full Text] [Related]
10. Partial monosomy 8p and partial trisomy 8p with moderate mental retardation.
van Balkom ID; Hagendoorn J; De Pater JM; Hennekam RC
Genet Couns; 1992; 3(2):83-9. PubMed ID: 1642815
[TBL] [Abstract][Full Text] [Related]
11. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Partial 8p trisomy due to interstitial duplication: karyotype: 46, XX, inv dup(8) (p21.1----p22).
Fryns JP; Kleczkowska A; Dereymaker AM; Hoefnagels M; Heremans G; Marien J; van den Berghe H
Clin Genet; 1985 Dec; 28(6):546-9. PubMed ID: 4075566
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.
Horn D; Neitzel H; Tönnies H; Kalscheuer V; Kunze J; Hinkel GK; Bartsch O
Am J Med Genet A; 2003 Mar; 117A(3):236-44. PubMed ID: 12599186
[TBL] [Abstract][Full Text] [Related]
16. [Cytogenetic analysis of partial trisomy 9p resulting from a reciprocal balanced 9/21 translocation].
Wang XR; Luo RL; Dai XH; Liu JY
Yi Chuan; 2007 Jul; 29(7):813-6. PubMed ID: 17646146
[TBL] [Abstract][Full Text] [Related]
17. Trisomy 3q25.1-qter and monosomy 8p23.1-pter in a patient: cytogenetic and molecular analysis with delineation of the phenotype.
Zafra de la Rosa G; Venegas-Vega CA; Monroy N; Contreras-Bucio G; Friedrich U; Houman M; Saad A; Fernández P; Kofman-Alfaro S; Cervantes A
Am J Med Genet A; 2005 Jul; 136(3):259-64. PubMed ID: 15957183
[TBL] [Abstract][Full Text] [Related]
18. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
Chen CP; Chern SR; Lin CC; Wang TH; Li YC; Hsieh LJ; Lee CC; Hua HM; Wang W
Prenat Diagn; 2006 Apr; 26(4):313-20. PubMed ID: 16506269
[TBL] [Abstract][Full Text] [Related]
19. Partial trisomy 8p (8p11.2-->pTER) and deletion of 13q (13q32-->qTER): case report.
Yeşilyurt A; Dilli D; Oguz S; Dilmen U; Altug N; Candemir Z
Genet Couns; 2011; 22(1):35-40. PubMed ID: 21614986
[TBL] [Abstract][Full Text] [Related]
20. Segregation of a paternal insertional translocation results in partial 4q monosomy or 4q trisomy in two siblings.
Hegmann KM; Spikes AS; Orr-Urtreger A; Shaffer LG
Am J Med Genet; 1996 Jan; 61(1):10-5. PubMed ID: 8741910
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]