173 related articles for article (PubMed ID: 31315112)
1. Small Supernumerary Ring Chromosome Derived from an Inverted Duplication of 13q11.2q14 in a Fetus with Coarctation of the Aorta.
Zeng J; Huang M; Lin J; Zhang X; Lan F
Cytogenet Genome Res; 2019; 158(4):199-204. PubMed ID: 31315112
[TBL] [Abstract][Full Text] [Related]
2. Tetrasomy 13q31.1qter due to an inverted duplicated neocentric marker chromosome in a fetus with multiple malformations.
Haddad V; Aboura A; Tosca L; Guediche N; Mas AE; L'Herminé AC; Druart L; Picone O; Brisset S; Tachdjian G
Am J Med Genet A; 2012 Apr; 158A(4):894-900. PubMed ID: 22419357
[TBL] [Abstract][Full Text] [Related]
3. First prenatally detected small supernumerary neocentromeric derivative chromosome 13 resulting in a non-mosaic partial tetrasomy 13q.
Mascarenhas A; Matoso E; Saraiva J; Tönnies H; Gerlach A; Julião MJ; Melo JB; Carreira IM
Cytogenet Genome Res; 2008; 121(3-4):293-7. PubMed ID: 18758175
[TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8.
Chen CP; Chen M; Ko TM; Ma GC; Tsai FJ; Tsai MS; Wu PC; Lee CC; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2010 Dec; 49(4):500-5. PubMed ID: 21199754
[TBL] [Abstract][Full Text] [Related]
5. Prenatal detection and characterization of a small supernumerary marker chromosome (sSMC) derived from chromosome 22 with apparently normal phenotype.
Lin CC; Hsieh YY; Wang CH; Li YC; Hsieh LJ; Lee CC; Tsai CH; Tsai FJ
Prenat Diagn; 2006 Oct; 26(10):898-902. PubMed ID: 16915592
[TBL] [Abstract][Full Text] [Related]
6. Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency.
Stembalska A; Jagielska G; Laczmanska I; Szmida E; Jarczynska A; Gil J
Birth Defects Res A Clin Mol Teratol; 2015 Apr; 103(4):255-9. PubMed ID: 25852029
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
Chen CP; Chen M; Chern SR; Wu PS; Chang SP; Lee DJ; Chen YT; Chen LF; Su JW; Hwa-Ruey Hsieh A; Hwa-Jiun Hsieh A; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):411-7. PubMed ID: 23040927
[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 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]
10. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
[TBL] [Abstract][Full Text] [Related]
11. [Prenatal diagnosis of a Pallister-Killian syndrome case through analysis of a supernumerary chromosome using single nucleotide polymorphism array].
Li S; Shen H; Jin Y; Liu X; Song Q; Miao Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct; 33(5):682-5. PubMed ID: 27577223
[TBL] [Abstract][Full Text] [Related]
12. [Prenatal diagnosis of three fetuses with small supernumerary marker chromosomes].
Li W; Fang R; Shen X; Yao J; Xue J; Shen G
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Dec; 37(12):1344-1348. PubMed ID: 33306818
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1-q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality.
Chen CP; Chern SR; Chen YN; Chen SW; Wu PS; Yang CW; Lee CC; Lee MS; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2017 Apr; 56(2):217-223. PubMed ID: 28420511
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review.
Chen CP; Chen M; Wu CH; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Chang SP; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2017 Aug; 56(4):554-557. PubMed ID: 28805618
[TBL] [Abstract][Full Text] [Related]
16. A novel combined 15q11.2 duplication and a bisatellited supernumerary marker derived from chromosome 22: molecular characterization of the marker.
Dutta UR; Vempally S; Ranganath P; Dalal A
Gene; 2014 Apr; 539(1):162-7. PubMed ID: 24508374
[TBL] [Abstract][Full Text] [Related]
17. Boy with bilateral retinoblastoma due to an unusual ring chromosome 13 with activation of a latent centromere.
Morrissette JD; Celle L; Owens NL; Shields CL; Zackai EH; Spinner NB
Am J Med Genet; 2001 Feb; 99(1):21-8. PubMed ID: 11170089
[TBL] [Abstract][Full Text] [Related]
18. Small supernumerary marker chromosome originating from chromosome 10 associated with an apparently normal phenotype.
Sung PL; Chang SP; Wen KC; Chang CM; Yang MJ; Chen LC; Chao KC; Huang CY; Li YC; Lin CC
Am J Med Genet A; 2009 Dec; 149A(12):2768-74. PubMed ID: 19921638
[TBL] [Abstract][Full Text] [Related]
19. [Prenatal diagnosis of a fetus with two small supernumerary marker chromosomes].
Zhang J; Jiang Y; Cai M; Ge Y; Zhou Y; Wang W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Dec; 36(12):1222-1225. PubMed ID: 31813153
[TBL] [Abstract][Full Text] [Related]
20. [Cytogenetic and molecular genetic analysis of small supernumerary marker chromosomes in fetal amniotic fluid].
Zhang W; Pan Y; Zhang Y; Dai M; Chen X; Shi W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):187-191. PubMed ID: 28397215
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]