183 related articles for article (PubMed ID: 11015707)
1. Prenatal diagnosis and genetic analysis of X chromosome polysomy 49, XXXXY.
Chen CP; Chern SR; Chang CL; Lee CC; Chen WL; Chen LF; Wang W
Prenat Diagn; 2000 Sep; 20(9):754-7. PubMed ID: 11015707
[TBL] [Abstract][Full Text] [Related]
2. Prenatal sonographic diagnosis of the 49,XXXXY syndrome.
Schluth C; Doray B; Girard-Lemaire F; Kohler M; Langer B; Gasser B; Lindner V; Flori E
Prenat Diagn; 2002 Dec; 22(13):1177-80. PubMed ID: 12478628
[TBL] [Abstract][Full Text] [Related]
3. A case of 48,XXYY syndrome detected prenatally by QF-PCR.
Zhang QS; Li DZ
J Matern Fetal Neonatal Med; 2009 Dec; 22(12):1214-6. PubMed ID: 19916722
[TBL] [Abstract][Full Text] [Related]
4. Increased nuchal translucency, hydrops fetalis or hygroma colli. A new test strategy for early fetal aneuploidy detection.
Jenderny J; Schmidt W; Hecher K; Hackelöer BJ; Kerber S; Kochhan L; Held KR
Fetal Diagn Ther; 2001; 16(4):211-4. PubMed ID: 11399881
[TBL] [Abstract][Full Text] [Related]
5. Sex chromosome pentasomy (49,XXXXY) presenting as cystic hygroma at 16 weeks' gestation.
Sepulveda W; Ivankovic M; Be C; Youlton R
Prenat Diagn; 1999 Mar; 19(3):257-9. PubMed ID: 10210125
[TBL] [Abstract][Full Text] [Related]
6. Rapid detection of chromosomes X and Y aneuploidies by quantitative fluorescent PCR.
Cirigliano V; Sherlock J; Conway G; Quilter C; Rodeck C; Adinolfi M
Prenat Diagn; 1999 Dec; 19(12):1099-103. PubMed ID: 10590424
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis and genetic analysis of double trisomy 48,XXX,+18.
Chen CP; Chern SR; Yeh LF; Chen WL; Chen LF; Wang W
Prenat Diagn; 2000 Sep; 20(9):750-3. PubMed ID: 11015706
[TBL] [Abstract][Full Text] [Related]
8. Incidence of chromosomal abnormalities in the presence of fetal subcutaneous oedema, such as nuchal oedema, cystic hygroma and non-immune hydrops.
Beke A; Joó JG; Csaba A; Lázár L; Bán Z; Papp C; Tóth-Pál E; Papp Z
Fetal Diagn Ther; 2009; 25(1):83-92. PubMed ID: 19218808
[TBL] [Abstract][Full Text] [Related]
9. Nonimmune hydrops fetalis in a 49,XXXXY fetus at 16 menstrual weeks.
Hovav Y; Nadjari M; Dagan J; Kafka E; Yaffe H
Am J Med Genet; 1993 Sep; 47(4):529-30. PubMed ID: 8256817
[No Abstract] [Full Text] [Related]
10. Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound.
Daniel A; Athayde N; Ogle R; George AM; Michael J; Pertile MD; Bryan J; Jammu V; Trudinger BJ
Aust N Z J Obstet Gynaecol; 2003 Feb; 43(1):16-26. PubMed ID: 12755342
[TBL] [Abstract][Full Text] [Related]
11. Outcome of cystic hygroma in fetuses with normal karyotypes depends on associated findings.
Tanriverdi HA; Ertan AK; Hendrik HJ; Remberger K; Schmidt W
Eur J Obstet Gynecol Reprod Biol; 2005 Jan; 118(1):40-6. PubMed ID: 15596271
[TBL] [Abstract][Full Text] [Related]
12. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb.
Chen CP; Chern SR; Chen CY; Wu PC; Chen LF; Pan CW; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):479-84. PubMed ID: 22212321
[TBL] [Abstract][Full Text] [Related]
13. Fetal axillary cystic hygroma: a novel association with triple X syndrome.
Iskender C; Tarım E; Cok T; Yalcinkaya C; Kalaycı H; Sahin F
Birth Defects Res A Clin Mol Teratol; 2012 Nov; 94(11):955-7. PubMed ID: 23109196
[TBL] [Abstract][Full Text] [Related]
14. Second-trimester cystic hygroma: prognosis of septated and nonseptated lesions.
Brumfield CG; Wenstrom KD; Davis RO; Owen J; Cosper P
Obstet Gynecol; 1996 Dec; 88(6):979-82. PubMed ID: 8942838
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
Chen CP; Chern SR; Wang TH; Hsueh DW; Lee CC; Town DD; Wang W; Ko TM
Prenat Diagn; 2005 Jun; 25(6):492-6. PubMed ID: 15966044
[TBL] [Abstract][Full Text] [Related]
16. A case report of Turner syndrome associated with fetal nuchal cystic hygroma and bilateral syndactyly of the hands and feet.
Chen HY; Zheng JQ; Zhang HP
Ital J Pediatr; 2019 Jul; 45(1):85. PubMed ID: 31319890
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Familial cystic hygroma. Report of 8 cases in 3 families.
Tricoire J; Sarramon MF; Rolland M; Lefort G
Genet Couns; 1993; 4(4):265-9. PubMed ID: 8110412
[TBL] [Abstract][Full Text] [Related]
19. Recurrent fetal cystic hygroma with normal chromosomes: case report and review of the literature.
Teague KE; Eggleston MK; Muffley PE; Gherman RB
J Matern Fetal Med; 2000; 9(6):366-9. PubMed ID: 11243297
[TBL] [Abstract][Full Text] [Related]
20. Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies.
Langlois S; Duncan A; ;
J Obstet Gynaecol Can; 2011 Sep; 33(9):955-960. PubMed ID: 21923994
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
