238 related articles for article (PubMed ID: 19262083)
1. [A case of mosaic ring chromosome 4 with subtelomeric 4p deletion].
Kim JH; Oh PS; Na HY; Kim SH; Cho HC
Korean J Lab Med; 2009 Feb; 29(1):77-81. PubMed ID: 19262083
[TBL] [Abstract][Full Text] [Related]
2. Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies.
Balci S; Engiz O; Aktaş D; Vargel I; Beksaç MS; Mrasek K; Vermeesch J; Liehr T
Am J Med Genet A; 2006 Mar; 140(6):628-32. PubMed ID: 16470698
[TBL] [Abstract][Full Text] [Related]
3. Molecular cytogenetic characterization of ring chromosome 4 in a female having a chromosomally normal child.
Lee MH; Park SY; Kim YM; Kim JM; Yoo KJ; Lee HH; Ryu HM
Cytogenet Genome Res; 2005; 111(2):175-8. PubMed ID: 16103661
[TBL] [Abstract][Full Text] [Related]
4. Interstitial deletion of distal chromosome 4p in a patient without classical Wolf-Hirschhorn syndrome.
Estabrooks LL; Rao KW; Korf B
Am J Med Genet; 1993 Jan; 45(1):97-100. PubMed ID: 8418669
[TBL] [Abstract][Full Text] [Related]
5. Wolf Hirshhorn syndrome in a case of ring chromosome 4: phenotype and molecular cytogenetic findings.
Laleye A; Alao MJ; Adjagba M; Hans C; Delneste D; Gnamey DK; Ayivi B; Darboux RB
Genet Couns; 2006; 17(1):35-40. PubMed ID: 16719275
[TBL] [Abstract][Full Text] [Related]
6. Familial interstitial deletion of the short arm of chromosome 4 (p15.33-p16.3) characterized by molecular cytogenetic analysis.
Basinko A; Douet-Guilbert N; Parent P; Blondin G; Mingam M; Monot F; Morel F; Le Bris MJ; De Braekeleer M
Am J Med Genet A; 2008 Apr; 146A(7):899-903. PubMed ID: 18302281
[TBL] [Abstract][Full Text] [Related]
7. Ring chromosome 4: Wolf syndrome and unspecific developmental anomalies.
Kosztolányi G
Acta Paediatr Hung; 1985; 26(2):157-65. PubMed ID: 4041283
[TBL] [Abstract][Full Text] [Related]
8. Ring Chromosome 9 and Chromosome 9p Deletion Syndrome in a Patient Associated with Developmental Delay: A Case Report and Review of the Literature.
Sivasankaran A; Kanakavalli MK; Anuradha D; Samuel CR; Kandukuri LR
Cytogenet Genome Res; 2016; 148(2-3):165-73. PubMed ID: 27222354
[TBL] [Abstract][Full Text] [Related]
9. FISH detection of Wolf-Hirschhorn syndrome: exclusion of D4F26 as critical site.
Johnson VP; Altherr MR; Blake JM; Keppen LD
Am J Med Genet; 1994 Aug; 52(1):70-4. PubMed ID: 7977466
[TBL] [Abstract][Full Text] [Related]
10. Ring chromosome 4 in a patient with early onset type 2 diabetes, deafness, and developmental delay.
Blackett PR; Li S; Mulvihill JJ
Am J Med Genet A; 2005 Aug; 137(2):213-6. PubMed ID: 16082703
[TBL] [Abstract][Full Text] [Related]
11. "Ring syndrome" involving chromosome 2 confirmed by FISH analysis using chromosome-specific subtelomeric probes.
Kosho T; Matsushima K; Sahashi T; Mitsui N; Fukushima Y; Sobajima H; Ohashi H
Genet Couns; 2005; 16(1):65-70. PubMed ID: 15844781
[TBL] [Abstract][Full Text] [Related]
12. Class II neocentromeres: a putative common neocentromere site in band 4q21.2.
Warburton PC; Barwell J; Splitt M; Maxwell D; Bint S; Ogilvie CM
Eur J Hum Genet; 2003 Oct; 11(10):749-53. PubMed ID: 14512964
[TBL] [Abstract][Full Text] [Related]
13. [Analysis of clinical and genetic characteristics of a child with ring chromosome 4 syndrome].
Lyu Y; Song F; Zhang K; Gao M; Ma J; Wang D; Wan Y; Liu Y; Gai Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Aug; 37(8):843-846. PubMed ID: 32761591
[TBL] [Abstract][Full Text] [Related]
14. High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
Fang YY; Bain S; Haan EA; Eyre HJ; MacDonald M; Wright TJ; Altherr MR; Riess O; Sutherland G; Callen DF
Am J Med Genet; 1997 Sep; 71(4):453-7. PubMed ID: 9286454
[TBL] [Abstract][Full Text] [Related]
15. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
[TBL] [Abstract][Full Text] [Related]
16. Clinical, cytogenetic and molecular study in a case of r(3) with 3p deletion and review of the literature.
Guilherme RS; Bragagnolo S; Pellegrino R; Christofolini DM; Takeno SS; Carvolheira GM; Kulikowski LD; Melaragno MI
Cytogenet Genome Res; 2011; 134(4):325-30. PubMed ID: 21849783
[TBL] [Abstract][Full Text] [Related]
17. Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter).
Calabrese G; Giannotti A; Mingarelli R; Di Gilio MC; Piemontese MR; Palka G
Clin Genet; 1997 Apr; 51(4):264-7. PubMed ID: 9184250
[TBL] [Abstract][Full Text] [Related]
18. Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome.
Sigurdardottir S; Goodman BK; Rutberg J; Thomas GH; Jabs EW; Geraghty MT
Am J Med Genet; 1999 Dec; 87(5):384-90. PubMed ID: 10594875
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13.
Chen CP; Tsai CH; Chern SR; Wu PS; Su JW; Lee CC; Chen YT; Chen WL; Chen LF; Wang W
Gene; 2013 Oct; 529(1):163-8. PubMed ID: 23933417
[TBL] [Abstract][Full Text] [Related]
20. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]