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.
124 related articles for article (PubMed ID: 8882791)
1. De novo interstitial tandem duplication of chromosome 4(q21-q28). Navarro EG; Romero MC; Expósito IL; Velasco CM; Llamas JG; Ramón FJ; Jimenez RD Am J Med Genet; 1996 Mar; 62(3):297-9. PubMed ID: 8882791 [TBL] [Abstract][Full Text] [Related]
2. Interstitial tandem direct duplication of the long arm of chromosome 4 (q23-q27) and possible assignment of the structural gene encoding human aspartylglucosaminidase to this segment. Halal F; Vekemans M; Chitayat D Am J Med Genet; 1991 Jun; 39(4):418-21. PubMed ID: 1877620 [TBL] [Abstract][Full Text] [Related]
3. Brief clinical report: interstitial deletion of the long arm of chromosome 4, del(4)(q28-->q31.3). Copelli S; del Rey G; Heinrich J; Coco R Am J Med Genet; 1995 Jan; 55(1):77-9. PubMed ID: 7702102 [TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion of 18q: comparative genomic hybridization array analysis of 46, XX,del(18)(q21.2.q21.33). Kato Z; Morimoto W; Kimura T; Matsushima A; Kondo N Birth Defects Res A Clin Mol Teratol; 2010 Feb; 88(2):132-5. PubMed ID: 19813260 [TBL] [Abstract][Full Text] [Related]
5. De novo duplication of 17p [dup(17)(p12----p11.2)]: report of an additional case with confirmation of the cytogenetic, phenotypic, and developmental aspects. Kozma C; Meck JM; Loomis KJ; Galindo HC Am J Med Genet; 1991 Dec; 41(4):446-50. PubMed ID: 1776635 [TBL] [Abstract][Full Text] [Related]
6. CHARGE association in a child with de novo inverted duplication (14)(q22-->q24.3). North KN; Wu BL; Cao BN; Whiteman DA; Korf BR Am J Med Genet; 1995 Jul; 57(4):610-4. PubMed ID: 7573139 [TBL] [Abstract][Full Text] [Related]
7. A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1). Mohrschladt MF; Bijlsma EK; Sluijter S; De Coo RF; Hoovers JM; Leschot NJ Clin Dysmorphol; 1999 Jul; 8(3):211-4. PubMed ID: 10457857 [TBL] [Abstract][Full Text] [Related]
8. De novo direct duplication 7p (p11.2-->pter) in an Arab child with MCA/MR syndrome: trisomy 7p a delineated syndrome? Redha MA; Krishna Murthy DS; al-Awadi SA; al-Sulaiman IS; Sabry MA; el-Bahey SA; Farag TI Ann Genet; 1996; 39(1):5-9. PubMed ID: 9297445 [TBL] [Abstract][Full Text] [Related]
9. De novo interstitial duplication 4(q28.1q35) associated with choanal atresia. Lin S; Kirk EP; McKenzie F; Francis C; Shalhoub C; Turner AM J Paediatr Child Health; 2004 Jul; 40(7):401-3. PubMed ID: 15228573 [TBL] [Abstract][Full Text] [Related]
10. Apparently nonmosaic trisomy 22: clinical report and review. Sundareshan TS; Naguib KK; al-Awadi SA; Redha MA; Hamoud MS Am J Med Genet; 1990 May; 36(1):7-10. PubMed ID: 2185636 [TBL] [Abstract][Full Text] [Related]
11. Further contribution to the description of phenotypes associated with partial 4q duplication. Zollino M; Zampino G; Torrioli G; Pomponi MG; Neri G Am J Med Genet; 1995 May; 57(1):69-73. PubMed ID: 7645603 [TBL] [Abstract][Full Text] [Related]
12. Duplication 10p in a girl due to a maternal translocation t(10;14) (p11:p12). Gonzalez CH; Billerbeck AE; Takayama LC; Wajntal A Am J Med Genet; 1983 Jan; 14(1):159-67. PubMed ID: 6829605 [TBL] [Abstract][Full Text] [Related]
13. [Del (13) (q33). Exclusion of esterase D (ESD) from 13q33 and q34]. Turleau C; Séger J; de Grouchy J; Doré F; Job JC Ann Genet; 1978 Sep; 21(3):189-92. PubMed ID: 315197 [TBL] [Abstract][Full Text] [Related]
14. Interstitial 6q duplication in an adult male without growth delay or severe mental retardation. Cappon SL; Duncan AM; Khalifa MM Med Sci Monit; 2000; 6(3):581-5. PubMed ID: 11208374 [TBL] [Abstract][Full Text] [Related]
15. Mild phenotype due to inverse duplication 4p16.3 - P15.3 including the Wolf-Hirschhorn critical region. Tschernigg M; Petek E; Wagner K; Kroisel PM Genet Couns; 2002; 13(1):29-33. PubMed ID: 12017235 [TBL] [Abstract][Full Text] [Related]
16. De novo dup(X)(q22.1q25) in a girl with an abnormal phenotype. Tihy F; Lemyre E; Lemieux N; Dallaire L Am J Med Genet; 1999 Dec; 87(4):302-5. PubMed ID: 10588834 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Interstitial duplication of 7(q22-->q34). Stratton RF; DuPont BR; Mattern VL; Schelonka RL; Moore CM Am J Med Genet; 1993 Sep; 47(3):380-2. PubMed ID: 8135285 [TBL] [Abstract][Full Text] [Related]
19. Duplication 10q confirmed by DNA in situ hybridization. Johnson VP; Sutliff WC Am J Med Genet; 1994 Aug; 52(2):184-7. PubMed ID: 7802006 [TBL] [Abstract][Full Text] [Related]
20. Functional disomy of the Xq28 chromosome region. Sanlaville D; Prieur M; de Blois MC; Genevieve D; Lapierre JM; Ozilou C; Picq M; Gosset P; Morichon-Delvallez N; Munnich A; Cormier-Daire V; Baujat G; Romana S; Vekemans M; Turleau C Eur J Hum Genet; 2005 May; 13(5):579-85. PubMed ID: 15741994 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]