These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
317 related articles for article (PubMed ID: 24751616)
1. Pure trisomy 2p syndrome in two siblings with an unbalanced translocation and minimal terminal 12q monosomy characterized by high-density microarray. Martínez-Juárez A; Uribe-Figueroa L; Quintana-Palma M; Razo-Aguilera G; Sevilla-Montoya R Cytogenet Genome Res; 2014; 142(4):249-54. PubMed ID: 24751616 [TBL] [Abstract][Full Text] [Related]
2. Subtelomeric 6p monosomy and 12q trisomy in a patient with a 46,XX,der(6)t(6;12)(p25.3;q24.31) karyotype: Phenotypic overlap with Mutchinick syndrome. Semerci CN; Cinbis M; Ullmann R; Steininger A; Bahce M; Yagci B; Ozden S; Sabir N; Gumus D; Tepeli E; Arteaga J; Mutchinick OM Am J Med Genet A; 2010 Jul; 152A(7):1724-9. PubMed ID: 20578131 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Partial monosomy 11q and trisomy 12q: variable expression in two siblings. Lukusa T; Holvoet M; Vermeesch JR; Devriendt K; Fryns JP Genet Couns; 2003; 14(2):155-64. PubMed ID: 12872809 [TBL] [Abstract][Full Text] [Related]
6. Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report. Tos T; Alp MY; Eker HK; Cebi AH; Ikbal M Genet Couns; 2014; 25(1):35-9. PubMed ID: 24783653 [TBL] [Abstract][Full Text] [Related]
7. Partial trisomy 2p24-->pter and monosomy 18q22.1- qter resulting from parental translocation. Atik T; Durmaz B; Yorganci OU; Cogulu O; Kioutsouk M; Ozkinay F Genet Couns; 2013; 24(2):179-84. PubMed ID: 24032288 [TBL] [Abstract][Full Text] [Related]
8. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter). Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278 [TBL] [Abstract][Full Text] [Related]
9. Familial distal monosomy 5p15.3-pter with trisomy 12q24.2-qter resulting in neurodevelopmental delay and dysmorphic features. Čiuladaitė Ž; Matulevičienė A; Bandanskytė A; Brazaitis A; Kasnauskienė J; Kučinskas V J Child Neurol; 2014 Mar; 29(3):399-405. PubMed ID: 23340083 [TBL] [Abstract][Full Text] [Related]
10. Partial 6q monosomy/partial 12q trisomy in a child with features of Kabuki make-up syndrome. Jardine PE; Burvill-Holmes LC; Schutt WH; Lunt PW Clin Dysmorphol; 1993 Jul; 2(3):269-73. PubMed ID: 8287190 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities. Cox DM; Butler MG Cytogenet Genome Res; 2015; 145(1):29-34. PubMed ID: 25871641 [TBL] [Abstract][Full Text] [Related]
14. Partial monosomy 2p and partial trisomy 4q due to paternal translocation t(2;4)(p25.1;q31.3). Skrlec I; Wagner J; Puseljić S; Heffer M; Stipoljev F Coll Antropol; 2014 Jun; 38(2):759-62. PubMed ID: 25145019 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Partial trisomy 3p and partial monosomy 11q associated with atrial septal defect, cleft palate, and developmental delay: a case report. Tan EC; Lim E; Cham B; Knight L; Ng I Cytogenet Genome Res; 2011; 134(4):319-24. PubMed ID: 21654159 [TBL] [Abstract][Full Text] [Related]
17. A 14-year follow-up of a case detected prenatally of partial trisomy 13q21.32-qter and monosomy 18q22.3-qter as a result of a maternal complex chromosome rearrangement involving chromosomes 6, 13, and 18. Quadrelli R; Quadrelli A; Milunsky A; Zou YS; Huang XL; Viera E; Mechoso B; Bellini S; Costabel M; Vaglio A Genet Test Mol Biomarkers; 2009 Jun; 13(3):387-93. PubMed ID: 19473082 [TBL] [Abstract][Full Text] [Related]
18. Clinical and molecular genetic characterization of two siblings with trisomy 2p24.3-pter and monosomy 5p14.3-pter. Fukushi D; Kurosawa K; Suzuki Y; Suzuki K; Yamada K; Watanabe S; Yokochi K; Wakamatsu N Am J Med Genet A; 2017 Aug; 173(8):2201-2209. PubMed ID: 28599099 [TBL] [Abstract][Full Text] [Related]