141 related articles for article (PubMed ID: 19921639)
1. Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy.
Soysal Y; Balci S; Hekimler K; Liehr T; Ewers E; Schoumans J; Bui TH; Içduygu FM; Kosyakova N; Imirzalioğlu N
Am J Med Genet A; 2009 Dec; 149A(12):2782-7. PubMed ID: 19921639
[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. [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]
4. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
Syrrou M; Borghgraef M; Fryns JP
Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
[TBL] [Abstract][Full Text] [Related]
5. Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9.
Chen CP; Chen M; Wang LK; Chern SR; Wu PS; Chen SW; Lai ST; Chang SP; Yang CW; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):527-533. PubMed ID: 28805612
[TBL] [Abstract][Full Text] [Related]
6. Array-CGH and clinical findings in a patient with a small supernumerary r(8) mosaicism.
Eyüpoğlu FC; Sünnetçi D; Cine N; Savli H; Okten A; Açikgöz EG; Sönmez FM
Genet Couns; 2014; 25(3):305-13. PubMed ID: 25365853
[TBL] [Abstract][Full Text] [Related]
7. Mosaic ring chromosome 14 and monosomy 14 presenting with growth retardation, epilepsy, and blepharophimosis.
Hou JW
Chang Gung Med J; 2004 May; 27(5):373-8. PubMed ID: 15366814
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities.
Chen CP; Lin SP; Lin YH; Chern SR; Wu PS; Chen YN; Chen SW; Yang CW; Chen WL; Wang W
Taiwan J Obstet Gynecol; 2016 Dec; 55(6):852-855. PubMed ID: 28040132
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [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]
11. Monosomy 8 rescue gave cells with a normal karyotype in a mildly affected man with 46,XY,r(8) mosaicism.
Gradek GA; Kvistad PH; Houge G
Eur J Med Genet; 2006; 49(4):292-7. PubMed ID: 16829350
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4.
Chen CP; Chen M; Su YN; Tsai FJ; Chern SR; Wu PC; Chen WL; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):188-95. PubMed ID: 21791306
[TBL] [Abstract][Full Text] [Related]
13. [Combined spectral karyotyping and microarray-based comparative genomic hybridization for the diagnosis of a case with ring chromosome 15].
Pan M; Choy KW; Liao C; Lau TK
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Oct; 29(5):562-5. PubMed ID: 23042394
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. De novo mosaic ring chromosome 18 in a child with mental retardation, epilepsy and immunological problems.
Lo-Castro A; El-Malhany N; Galasso C; Verrotti A; Nardone AM; Postorivo D; Palmieri C; Curatolo P
Eur J Med Genet; 2011; 54(3):329-32. PubMed ID: 21333764
[TBL] [Abstract][Full Text] [Related]
16. An epileptic case with mosaic ring chromosome 6 and 6q terminal deletion.
Kara N; Okten G; Guneş SO; Saglam Y; Tasdemir HA; Pinarli FA
Epilepsy Res; 2008 Aug; 80(2-3):219-23. PubMed ID: 18485670
[TBL] [Abstract][Full Text] [Related]
17. Ring chromosome 20 with loss of telomeric sequences detected by multicolour PRINS.
Brandt CA; Kierkegaard O; Hindkjaer J; Jensen PK; Pedersen S; Therkelsen AJ
Clin Genet; 1993 Jul; 44(1):26-31. PubMed ID: 8403451
[TBL] [Abstract][Full Text] [Related]
18. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
[TBL] [Abstract][Full Text] [Related]
19. Characterization of a de novo Supernumerary Neocentric Ring Chromosome Derived from Chromosome 7.
Louvrier C; Egea G; Labalme A; Des Portes V; Gazzo S; Callet-Bauchu E; Till M; Sanlaville D; Edery P; Schluth-Bolard C
Cytogenet Genome Res; 2015; 147(2-3):111-7. PubMed ID: 26669311
[TBL] [Abstract][Full Text] [Related]
20. Mosaic trisomy of a small r(1) with an abnormal phenotype.
Dawson AJ; Konkin D; Riordan D; Chudley AE
Am J Med Genet; 2001 Sep; 103(1):32-5. PubMed ID: 11562931
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]