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.
206 related articles for article (PubMed ID: 10528239)
1. Proximal 5p trisomy resulting from a marker chromosome implicates band 5p13 in 5p trisomy syndrome. Avansino JR; Dennis TR; Spallone P; Stock AD; Levin ML Am J Med Genet; 1999 Nov; 87(1):6-11. PubMed ID: 10528239 [TBL] [Abstract][Full Text] [Related]
2. Supernumerary marker chromosomes 5: confirmation of a critical region and resultant phenotype. D'Amato Sizonenko L; Ng D; Oei P; Winship I Am J Med Genet; 2002 Jul; 111(1):19-26. PubMed ID: 12124728 [TBL] [Abstract][Full Text] [Related]
3. Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen. Schuffenhauer S; Kobelt A; Daumer-Haas C; Löffler C; Müller G; Murken J; Meitinger T Am J Med Genet; 1996 Oct; 65(1):56-9. PubMed ID: 8914742 [TBL] [Abstract][Full Text] [Related]
4. Cytogenetic and molecular analysis in trisomy 12p. Allen TL; Brothman AR; Carey JC; Chance PF Am J Med Genet; 1996 May; 63(1):250-6. PubMed ID: 8723118 [TBL] [Abstract][Full Text] [Related]
5. [A new case of trisomy 5p]. Antonenko VG; Levina LIa; Chudnova VI Genetika; 1985 Dec; 21(12):2066-70. PubMed ID: 4085794 [TBL] [Abstract][Full Text] [Related]
7. [Trisomy 5p due to paternal translocation (4;5) (q35;p12)]. Menéndez I; Casaña H Bol Med Hosp Infant Mex; 1993 Mar; 50(3):194-6. PubMed ID: 8442884 [TBL] [Abstract][Full Text] [Related]
8. 3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema. Further characterization of the dup(5p13) syndrome. Oexle K; Hempel M; Jauch A; Meitinger T; Rivera-Brugués N; Stengel-Rutkowski S; Strom T Eur J Med Genet; 2011; 54(3):225-30. PubMed ID: 21211577 [TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of partial trisomy 14q (14q31.1-->qter) and partial monosomy 5p (5p13.2-->pter) associated with polyhydramnios, short limbs, micropenis and brain malformations. Chen CP; Chern SR; Tsai EJ; Lee CC; Chen LF; Wang W Genet Couns; 2009; 20(3):281-8. PubMed ID: 19852436 [No Abstract] [Full Text] [Related]
10. A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome. Loscalzo ML; Becker TA; Sutcliffe M Eur J Med Genet; 2008; 51(1):54-60. PubMed ID: 18006398 [TBL] [Abstract][Full Text] [Related]
11. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies. Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467 [TBL] [Abstract][Full Text] [Related]
12. Apparent Opitz BBBG syndrome with a partial duplication of 5p. Leichtman LG; Werner A; Bass WT; Smith D; Brothman AR Am J Med Genet; 1991 Aug; 40(2):173-6. PubMed ID: 1897571 [TBL] [Abstract][Full Text] [Related]
13. Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3). Hodge JC; Lawson-Yuen A; Stoler JM; Ligon AH Cytogenet Genome Res; 2007; 119(1-2):15-20. PubMed ID: 18160776 [TBL] [Abstract][Full Text] [Related]
14. Delineation of a supernumerary marker chromosome utilizing a multimodal approach of G-banding, fluorescent in situ hybridization, confirmatory P1 artificial chromosome fluorescent in situ hybridization, and high-resolution comparative genomic hybridization. Mark HF; Wyandt H; Huang XL; Milunsky JM Clin Genet; 2005 Aug; 68(2):146-51. PubMed ID: 15996211 [TBL] [Abstract][Full Text] [Related]
15. [Trisomy 5p: a report of 2 cases]. Alvarez-Coca J; García-Alix A; Delicado A; González M; Escribá R; López Pajares I; Morena V; Peralta A An Esp Pediatr; 1985 Mar; 22(4):288-92. PubMed ID: 4003955 [TBL] [Abstract][Full Text] [Related]
16. Stillborn baby with partial monosomy of the short arm of chromosome 5 and partial trisomy of the short arm of chromosome 20. Okada M; Usami A; Okajima K; Yamada M; Yamaguchi Y; Umezaki I; Matsuda Y; Ohta H Congenit Anom (Kyoto); 2005 Dec; 45(4):161-4. PubMed ID: 16359498 [TBL] [Abstract][Full Text] [Related]
17. De novo complete trisomy 5p: clinical and neuroradiological findings. Grosso S; Cioni M; Garibaldi G; Pucci L; Galluzzi P; Canapicchi R; Morgese G; Balestri P Am J Med Genet; 2002 Sep; 112(1):56-60. PubMed ID: 12239721 [TBL] [Abstract][Full Text] [Related]
18. Characterization of a de novo complex chromosomal rearrangement in a patient with cri-du-chat and trisomy 5p syndromes. Vera-Carbonell A; Bafalliu JA; Guillén-Navarro E; Escalona A; Ballesta-Martínez MJ; Fuster C; Fernández A; López-Expósito I Am J Med Genet A; 2009 Nov; 149A(11):2513-21. PubMed ID: 19842199 [TBL] [Abstract][Full Text] [Related]
19. Mosaic 5p tetrasomy. Stanley WS; Powell CM; Devine GC; Ellingham T; Samango-Sprouse CA; Vaught DR; Murphy BA; Rosenbaum KN Am J Med Genet; 1993 Mar; 45(6):774-6. PubMed ID: 8456861 [TBL] [Abstract][Full Text] [Related]
20. Phenotypic and cytogenetic spectrum of 9p trisomy. Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]