145 related articles for article (PubMed ID: 26759849)
1. Increased Fetal Nuchal Translucency - Also a Risk for a Rare Submicroscopic Chromosomal Abnormalities.
Tercanli S; Miny P; Filges I
Ultraschall Med; 2015 Oct; 36(5):419-20. PubMed ID: 26759849
[No Abstract] [Full Text] [Related]
2. 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]
3. Submicroscopic chromosomal abnormalities in fetuses with increased nuchal translucency and normal karyotype.
Yang X; Li R; Fu F; Zhang Y; Li D; Liao C
J Matern Fetal Neonatal Med; 2017 Jan; 30(2):194-198. PubMed ID: 26998667
[TBL] [Abstract][Full Text] [Related]
4. First trimester prenatal diagnosis of 13q-syndrome presenting with increased nuchal translucency, Dandy-Walker malformation and small parietal encephalocoele.
Hindryckx A; De Catte L; Van Esch H; Fryns JP; Moerman P; Devlieger R
Prenat Diagn; 2008 May; 28(5):445-6. PubMed ID: 18395870
[No Abstract] [Full Text] [Related]
5. [Increased nuchal translucency and cystic hygroma in the first trimester: prenatal diagnosis and neonatal outcome].
Ducarme G; Graesslin O; Alanio E; Bige V; Gaillard D; Gabriel R
Gynecol Obstet Fertil; 2005 Oct; 33(10):750-4. PubMed ID: 16139544
[TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of polysplenia syndrome associated with increased nuchal translucency.
Koyama S; Tomimatsu T; Kanagawa T; Morimoto A; Kimura T
Prenat Diagn; 2010 Oct; 30(10):1005-6. PubMed ID: 20721874
[No Abstract] [Full Text] [Related]
7. First-trimester ultrasound diagnosis of Meckel-Grüber syndrome.
Liu SS; Cheong ML; She BQ; Tsai MS
Acta Obstet Gynecol Scand; 2006; 85(6):757-9. PubMed ID: 16752273
[No Abstract] [Full Text] [Related]
8. Prenatal diagnosis of a supernumerary aberrant chromosome 9.
Hengstschläger M; Bettelheim D; Dörfler-Grassauer D; Prusa AR; Drahonsky R; Deutinger J; Bernaschek G
Arch Gynecol Obstet; 2003 Aug; 268(3):248-50. PubMed ID: 12942262
[TBL] [Abstract][Full Text] [Related]
9. Abnormal first trimester screen in partial deletion of chromosome 6p21: a case-report.
Hulsbergen MH; Van Calenbergh SG; Fryns JP
Genet Couns; 2007; 18(2):243-5. PubMed ID: 17710877
[TBL] [Abstract][Full Text] [Related]
10. Increased nuchal translucency and split-hand/foot malformation in a fetus with an interstitial deletion of chromosome 2q that removes the SHFM5 locus.
Bijlsma EK; Knegt AC; Bilardo CM; Goodman FR
Prenat Diagn; 2005 Jan; 25(1):39-44. PubMed ID: 15662696
[TBL] [Abstract][Full Text] [Related]
11. [Outcome of fetuses with malformations discovered before 14 weeks. Where the discovery is revealed by echography during the first trimester, is it responsible for the voluntary termination of the pregnancy? Comparison before and after July 2001].
Mangione R; Fries N; Godard P; Fontanges M; Haddad G; Mirlesse V;
J Gynecol Obstet Biol Reprod (Paris); 2008 Apr; 37(2):154-62. PubMed ID: 18036748
[TBL] [Abstract][Full Text] [Related]
12. Ultrasonographic markers for chromosomal abnormalities in women with negative nuchal translucency and second trimester maternal serum biochemistry.
Verdin SM; Whitlow BJ; Lazanakis M; Kadir RA; Chatzipapas I; Economides DL
Ultrasound Obstet Gynecol; 2000 Oct; 16(5):402-6. PubMed ID: 11169322
[TBL] [Abstract][Full Text] [Related]
13. RETIRED: Fetal soft markers in obstetric ultrasound.
Van den Hof MC; Wilson RD; ;
J Obstet Gynaecol Can; 2005 Jun; 27(6):592-636. PubMed ID: 16100637
[TBL] [Abstract][Full Text] [Related]
14. Diagnosis and management of fetal nuchal translucency.
Jackson M; Rose NC
Semin Roentgenol; 1998 Oct; 33(4):333-8. PubMed ID: 9800243
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Relation between increased fetal nuchal translucency thickness and chromosomal defects.
Kagan KO; Avgidou K; Molina FS; Gajewska K; Nicolaides KH
Obstet Gynecol; 2006 Jan; 107(1):6-10. PubMed ID: 16394033
[TBL] [Abstract][Full Text] [Related]
17. Nuchal translucency and other first-trimester sonographic markers of chromosomal abnormalities.
Nicolaides KH
Am J Obstet Gynecol; 2004 Jul; 191(1):45-67. PubMed ID: 15295343
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Ultrasound screening for Down syndrome and other chromosomal abnormalities by fetal nuchal translucency measurement between 11-14 weeks of gestation].
Dimitrova V; Markov D; Chernev T; Karag'ozova Zh; Mazneĭkova V; Andonova S; Vŭzharova R
Akush Ginekol (Sofiia); 2005; 44(1):32-7. PubMed ID: 15853009
[TBL] [Abstract][Full Text] [Related]
20. Prenatal diagnosis of Pallister-Killian syndrome in two fetuses with increased nuchal translucency.
Kim MH; Park SY; Kim MY; Lee BY; Lee MH; Ryu HM
Prenat Diagn; 2008 May; 28(5):454-6. PubMed ID: 18438966
[No Abstract] [Full Text] [Related]
[Next] [New Search]
