178 related articles for article (PubMed ID: 25852029)
1. 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]
2. Partial monosomy 13q (13q21.32--->qter) and partial trisomy 8p (8p1--->pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization.
Chen CP; Su YN; Tsai FJ; Lin MH; Wu PC; Chern SR; Lee CC; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):205-11. PubMed ID: 21791309
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Prenatal diagnosis of proximal partial trisomy 1q confirmed by comparative genomic hybridization array: molecular cytogenetic analysis, fetal pathology and review of the literature.
Sifakis S; Eleftheriades M; Kappou D; Murru R; Konstantinidou A; Orru S; Ziegler M; Liehr T; Manolakos E; Papoulidis I
Birth Defects Res A Clin Mol Teratol; 2014 Apr; 100(4):284-93. PubMed ID: 24677675
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
Brisset S; Kasakyan S; L'Herminé AC; Mairovitz V; Gautier E; Aubry MC; Benkhalifa M; Tachdjian G
Prenat Diagn; 2006 Mar; 26(3):206-13. PubMed ID: 16450348
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of a case of partial monosomy/monosomy 13 mosaicism: 46,XX,r(13)(p11q33)/45,XX,-13 suspected by nuchal fold translucency increasing.
Kataoka A; Hirakawa S; Iwamoto M; Sakumura Y; Yoshinaga R; Ohba T
Kurume Med J; 2011; 58(4):127-30. PubMed ID: 23047142
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. [Birth defects associated with increased nuchal translucency].
Mendoza-Caamal EC; Grether-González P; Hernández-Gómez M; Guzmán-Huerta M; Aguinaga-Ríos M
Ginecol Obstet Mex; 2010 Oct; 78(10):533-9. PubMed ID: 21966770
[TBL] [Abstract][Full Text] [Related]
10. Increased nuchal translucency in the presence of normal chromosomes: what's next?
Alamillo CM; Fiddler M; Pergament E
Curr Opin Obstet Gynecol; 2012 Mar; 24(2):102-8. PubMed ID: 22277886
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature.
Hu XN; Li LL; Shi QY; Hu ZM; Zhang HG; Jiang YT; Liu RZ
Taiwan J Obstet Gynecol; 2021 May; 60(3):554-558. PubMed ID: 33966748
[TBL] [Abstract][Full Text] [Related]
12. 3q26.31-q29 duplication and 9q34.3 microdeletion associated with omphalocele, ventricular septal defect, abnormal first-trimester maternal serum screening and increased nuchal translucency: prenatal diagnosis and aCGH characterization.
Chen CP; Lin CJ; Chen YY; Wang LK; Chern SR; Wu PS; Su JW; Chen LF; Town DD; Pan CW; Wang W
Gene; 2013 Dec; 532(1):80-6. PubMed ID: 24055486
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of a partial trisomy 13q (q14-->qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization.
Machado IN; Heinrich JK; Campanhol C; Rodrigues-Peres RM; Oliveira FM; Barini R
Genet Mol Res; 2010 Mar; 9(1):441-8. PubMed ID: 20391329
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome.
Chen CP; Ko TM; Chen YY; Su JW; Wang W
Gene; 2013 Sep; 527(1):384-8. PubMed ID: 23747353
[TBL] [Abstract][Full Text] [Related]
16. Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.
Sohn YB; Yun JN; Park SJ; Park MS; Kim SH; Lee JH
Ann Clin Lab Sci; 2013; 43(3):332-6. PubMed ID: 23884231
[TBL] [Abstract][Full Text] [Related]
17. First trimester diagnosis of 13q-syndrome associated with increased fetal nuchal translucency thickness. Clinical findings and systematic review.
Manolakos E; Peitsidis P; Garas A; Vetro A; Eleftheriades M; Petersen MB; Papoulidis I
Clin Exp Obstet Gynecol; 2012; 39(1):118-21. PubMed ID: 22675970
[TBL] [Abstract][Full Text] [Related]
18. A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13.2-q21.31 associated with multiple congenital abnormalities in a male fetus.
Sismani C; Donoghue J; Alexandrou A; Karkaletsi M; Christopoulou S; Konstantinidou AE; Livanos P; Patsalis PC; Velissariou V
Gene; 2013 Nov; 530(1):138-42. PubMed ID: 23973723
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of a small supernumerary, XIST-negative, mosaic ring X chromosome identified by fluorescence in situ hybridization in an abnormal male fetus.
Le Caignec C; Boceno M; Joubert M; Winer N; Aubron F; Fallet-Bianco C; Rival JM
Prenat Diagn; 2003 Feb; 23(2):143-5. PubMed ID: 12575022
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of the 13q-syndrome through three-dimensional ultrasonography: a case report.
Araujo Júnior E; Filho HA; Pires CR; Filho SM
Arch Gynecol Obstet; 2006 Jul; 274(4):243-5. PubMed ID: 16491370
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
