128 related articles for article (PubMed ID: 23421081)
1. [Frequency of prevalence of Turner syndrome in fetuses of patients referred to genetic amniocentesis in 2007-2011].
Chuchracki M; Szczepaniak A; Sedziak A; Ziółkowska K; Opala T
Przegl Lek; 2012; 69(10):1011-4. PubMed ID: 23421081
[TBL] [Abstract][Full Text] [Related]
2. Multiple marker screening test: identification of fetal cystic hygroma, hydrops, and sex chromosome aneuploidy.
Wenstrom KD; Boots LR; Cosper PC
J Matern Fetal Med; 1996; 5(1):31-5. PubMed ID: 8796763
[TBL] [Abstract][Full Text] [Related]
3. [Edwards syndrome--most frequent indications for genetic amniocentesis. Analysis of the last 5 years].
Chuchracki M; Janiak J; Ziółkowska K; Sedziak A; Opala T
Przegl Lek; 2012; 69(10):1007-10. PubMed ID: 23421080
[TBL] [Abstract][Full Text] [Related]
4. Prenatal and postnatal prevalence of Turner's syndrome: a registry study.
Gravholt CH; Juul S; Naeraa RW; Hansen J
BMJ; 1996 Jan; 312(7022):16-21. PubMed ID: 8555850
[TBL] [Abstract][Full Text] [Related]
5. Prenatally diagnosed Turner syndrome and cystic hygroma: incidence and reasons for referrals.
Alpman A; Cogulu O; Akgul M; Arikan EA; Durmaz B; Karaca E; Sağol S; Ozkinay C; Ozkinay F
Fetal Diagn Ther; 2009; 25(1):58-61. PubMed ID: 19202339
[TBL] [Abstract][Full Text] [Related]
6. A false-positive diagnosis of Turner syndrome by amniocentesis.
Griffiths MJ; Miller PR; Stibbe HM
Prenat Diagn; 1996 May; 16(5):463-6. PubMed ID: 8844007
[TBL] [Abstract][Full Text] [Related]
7. [Prenatal and postnatal prevalence of Turner syndrome. A registry-based study].
Gravholt CH; Juul S; Naeraa RW; Hansen J
Ugeskr Laeger; 1997 May; 159(21):3160-6. PubMed ID: 9199004
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of heterokaryotypic mosaic twins discordant for fetal sex.
Schmid O; Trautmann U; Ashour H; Ulmer R; Pfeiffer RA; Beinder E
Prenat Diagn; 2000 Dec; 20(12):999-1003. PubMed ID: 11113914
[TBL] [Abstract][Full Text] [Related]
9. Cytogenetic evaluation of fetal death: the role of amniocentesis.
Saal HM; Rodis J; Weinbaum PJ; DiMaggio R; Landrey TM
Obstet Gynecol; 1987 Oct; 70(4):601-3. PubMed ID: 2957622
[TBL] [Abstract][Full Text] [Related]
10. Spontaneous resolution of fetal cystic hygroma and hydrops in Turner syndrome.
Mostello DJ; Bofinger MK; Siddiqi TA
Obstet Gynecol; 1989 May; 73(5 Pt 2):862-5. PubMed ID: 2649827
[TBL] [Abstract][Full Text] [Related]
11. Cystic hygromas associated with Turner's syndrome. Report of three cases.
Kassanos D; Botsis D; Pyrgiotis E; Salamalekis E; Giannaki G; Zourlas PA
Clin Exp Obstet Gynecol; 1992; 19(4):222-5. PubMed ID: 1294342
[TBL] [Abstract][Full Text] [Related]
12. Second trimester prenatal diagnosis of epignathus teratoma in ring X chromosome mosaicism with inactive ring X chromosome.
Witters I; Moerman P; Louwagie D; Van Assche FA; Migeon BR; Fryns JP
Ann Genet; 2001; 44(4):179-82. PubMed ID: 11755101
[TBL] [Abstract][Full Text] [Related]
13. [Turner syndrome in the hôpital du Mali, a case].
Sow DS; Bah M; Traoré D; Dante ML; Mariko M; Traoré B; N'Diaye HD; Doumbia N; Sidibé AT
Mali Med; 2018; 33(2):21-22. PubMed ID: 30484580
[TBL] [Abstract][Full Text] [Related]
14. Ultrasonographic features of the fetal Turner syndrome.
Brown BS; Thompson DL
J Can Assoc Radiol; 1984 Mar; 35(1):40-6. PubMed ID: 6725367
[TBL] [Abstract][Full Text] [Related]
15. Elevated alpha-fetoprotein levels in the 45,x (Turner syndrome) fetus with cystic hygroma. Case reports.
Rosendorff J; Mayo JR; Reichman P; Pinto MR; Bernstein R
S Afr Med J; 1982 Oct; 62(17):621-4. PubMed ID: 6181571
[TBL] [Abstract][Full Text] [Related]
16. Outcome of fetuses with Turner syndrome: a 10-year congenital anomaly register based study.
Iyer NP; Tucker DF; Roberts SH; Moselhi M; Morgan M; Matthes JW
J Matern Fetal Neonatal Med; 2012 Jan; 25(1):68-73. PubMed ID: 21463211
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling.
Gilbert B; Yardin C; Briault S; Belin V; Lienhardt A; Aubard Y; Battin J; Servaud M; Philippe HJ; Lacombe D
Prenat Diagn; 2002 Aug; 22(8):697-702. PubMed ID: 12210579
[TBL] [Abstract][Full Text] [Related]
18. The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey.
Ataman E; Cogulu O; Durmaz A; Karaca E; Durmaz B; Akin H; Ozkinay F
Genet Test Mol Biomarkers; 2012 Feb; 16(2):150-3. PubMed ID: 21977968
[TBL] [Abstract][Full Text] [Related]
19. Turner syndrome: evaluation of prenatal diagnosis in 19 European registries.
Baena N; De Vigan C; Cariati E; Clementi M; Stoll C; Caballín MR; Guitart M
Am J Med Genet A; 2004 Aug; 129A(1):16-20. PubMed ID: 15266609
[TBL] [Abstract][Full Text] [Related]
20. Usefulness of fluorescence in situ hybridization for the diagnosis of Turner mosaic fetuses with small ring X chromosomes.
Siffroi JP; Dupuy O; Joye N; Le Bourhis C; Benzacken B; Portnoi M; Berkane N; Franco JC; Studer C; Carbonne B; Gonzales M; Bucourt M; Uzan S; Uzan M; Milliez J; Wolf JP; Taillemite J; Dadoune JP
Fetal Diagn Ther; 2000; 15(4):229-33. PubMed ID: 10867485
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
