149 related articles for article (PubMed ID: 23047142)
1. 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]
2. 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]
3. 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]
4. 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]
5. [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]
6. [Results of cytogenetic examinations in fetuses with increased nuchal translucency].
Kornacki J; Ziółkowska K; Goździewicz T; Skrzypczak J
Ginekol Pol; 2012 Mar; 83(3):189-93. PubMed ID: 22568194
[TBL] [Abstract][Full Text] [Related]
7. Increased nuchal translucency thickness and normal karyotype: time for parental reassurance.
Bilardo CM; Müller MA; Pajkrt E; Clur SA; van Zalen MM; Bijlsma EK
Ultrasound Obstet Gynecol; 2007 Jul; 30(1):11-8. PubMed ID: 17559183
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome.
Huynh MT; Riteau AS; Moradkhani K; Pichon O; Richard S; Joubert M; Bézieau S
Eur J Med Genet; 2021 Jan; 64(1):104118. PubMed ID: 33248287
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1 → pter) and 14q (14q32.31 → qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction, and single umbilical artery: prenatal diagnosis and molecular cytogenetic characterization.
Chen CP; Fu CH; Chern SR; Wu PS; Su JW; Lee CC; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2013 Sep; 52(3):401-6. PubMed ID: 24075381
[TBL] [Abstract][Full Text] [Related]
12. Trisomies and other chromosome abnormalities detected after positive sonographic findings.
Beke A; Papp C; Tóth-Pál E; Mezei G; Joó JG; Csaba A; Papp Z
J Reprod Med; 2005 Sep; 50(9):675-91. PubMed ID: 16363756
[TBL] [Abstract][Full Text] [Related]
13. Del(18p) syndrome with increased nuchal translucency in prenatal diagnosis.
Kim YM; Cho EH; Kim JM; Lee MH; Park SY; Ryu HM
Prenat Diagn; 2004 Mar; 24(3):161-4. PubMed ID: 15057945
[TBL] [Abstract][Full Text] [Related]
14. Prenatal detection of a subtle unbalanced chromosome rearrangement by karyotyping, FISH and array comparative genomic hybridization.
Cain CC; Saul DO; Oehler E; Blakemore K; Stetten G
Fetal Diagn Ther; 2008; 24(3):286-90. PubMed ID: 18818501
[TBL] [Abstract][Full Text] [Related]
15. Recurrent enlarged nuchal translucency: first trimester presentation of a familial 15q26→qter deletion.
Reiss R; Ahern D; Sandstrom M; Wilkins-Haug L
Am J Med Genet A; 2015 Mar; 167A(3):612-6. PubMed ID: 25691414
[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. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q (2q31.1-q32.1) encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency.
Chen CP; Lin CJ; Chen YN; Chern SR; Chen SW; Lai ST; Wu PS; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2017 Jun; 56(3):398-401. PubMed ID: 28600059
[TBL] [Abstract][Full Text] [Related]
18. The significance of anterolateral neck cysts in early diagnosis of fetal malformations.
Meyberg-Solomayer G; Hamza A; Takacs Z; Leingartner A; Radosa J; Joukhadar R; Juhasz-Böss I; Solomayer EF
Prenat Diagn; 2016 Apr; 36(4):332-7. PubMed ID: 26847019
[TBL] [Abstract][Full Text] [Related]
19. Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype.
Leung TY; Vogel I; Lau TK; Chong W; Hyett JA; Petersen OB; Choy KW
Ultrasound Obstet Gynecol; 2011 Sep; 38(3):314-9. PubMed ID: 21400624
[TBL] [Abstract][Full Text] [Related]
20. Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
Beulen L; Faas BHW; Feenstra I; van Vugt JMG; Bekker MN
Ultrasound Obstet Gynecol; 2017 Jun; 49(6):721-728. PubMed ID: 27515011
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
