116 related articles for article (PubMed ID: 16566037)
1. Cystic hygroma and omphalocele at 11 weeks in a fetus with monosomy X.
Goldstein I; Drugan A
Prenat Diagn; 2006 Apr; 26(4):381-2. PubMed ID: 16566037
[No Abstract] [Full Text] [Related]
2. Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q.
Chen CP; Lee CC; Chuang CY; Town DD; Lee MS; Chen MH
Clin Genet; 1997 Sep; 52(3):196-8. PubMed ID: 9377814
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome.
Chen CP; Chang SY; Lau HS; Chen SW; Lai ST; Chuang TY; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2018 Oct; 57(5):763-764. PubMed ID: 30342669
[No Abstract] [Full Text] [Related]
6. Prenatal diagnosis of Pentalogy of Cantrell in the first trimester: is 3-dimensional sonography needed?
Peixoto-Filho FM; do Cima LC; Nakamura-Pereira M
J Clin Ultrasound; 2009 Feb; 37(2):112-4. PubMed ID: 18506752
[TBL] [Abstract][Full Text] [Related]
7. Prenatal diagnosis of partial trisomy 3q(3q22-->qter) and monosomy 6q(6q25.3-->qter) in a fetus with sonographic findings of cystic hygromata colli and unilateral pleural effusion.
Chen CP
Prenat Diagn; 2001 Jan; 21(1):73. PubMed ID: 11180248
[No Abstract] [Full Text] [Related]
8. 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]
9. Prenatally detected interstitial deletion 13q12.3-q22 in a fetus with a cystic hygroma.
Vičić A; Zudenigo D; Korać P; Liehr T; Stipoljev F
Gene; 2013 Nov; 531(1):90-1. PubMed ID: 23999188
[No Abstract] [Full Text] [Related]
10. Monosomy X and omphalocele.
Govaerts LC; Bongers MY; Lammens MM; Tuerlings JH; van de Kaa CA
Prenat Diagn; 1997 Mar; 17(3):282. PubMed ID: 9110374
[No Abstract] [Full Text] [Related]
11. Natural history and outcome of prenatally diagnosed cystic hygroma.
Ganapathy R; Guven M; Sethna F; Vivekananda U; Thilaganathan B
Prenat Diagn; 2004 Dec; 24(12):965-8. PubMed ID: 15614877
[TBL] [Abstract][Full Text] [Related]
12. First-trimester septated cystic hygroma and cavum velum interpositum cyst.
Sherer DM; Dalloul M; Miller MJ; Kheyman M; Zinn HL; Abulafia O
J Clin Ultrasound; 2011 Jul; 39(6):356-8. PubMed ID: 21538378
[TBL] [Abstract][Full Text] [Related]
13. [Prenatal diagnosis of fetal nuchal cystic hygroma in 22 cases].
Du J; Qu L; Guo S
Zhonghua Fu Chan Ke Za Zhi; 1997 Jul; 32(7):425-7. PubMed ID: 9639731
[TBL] [Abstract][Full Text] [Related]
14. Fetus with a 9q22q34 interstitial deletion and hygroma.
Paoloni-Giacobino A; Floris E; Dahoun SP
Prenat Diagn; 2000 Oct; 20(10):855-6. PubMed ID: 11038472
[No Abstract] [Full Text] [Related]
15. Ruptured omphalocele with extracorporeal intestines mimicking gastroschisis in a fetus with Turner syndrome.
Chen CP
Prenat Diagn; 2007 Nov; 27(11):1067-8. PubMed ID: 17694577
[No Abstract] [Full Text] [Related]
16. [Ultrasonographic diagnosis of cystic hygroma at the 15th week. A case report].
Delzanno G; Gaudiano L
Minerva Ginecol; 1996 Sep; 48(9):375-6. PubMed ID: 8999385
[TBL] [Abstract][Full Text] [Related]
17. [Cystic hygroma. Antenatal diagnosis and clinical management].
Ruiz M; Figueroa J; Herrera M; Vargas V; Echeverría P; Ocaranza M
Rev Chil Obstet Ginecol; 1994; 59(6):428-33; discussion 433-4. PubMed ID: 7569162
[TBL] [Abstract][Full Text] [Related]
18. Karyotype and outcome of fetuses diagnosed with cystic hygroma in the first trimester in relation to nuchal translucency thickness.
Kharrat R; Yamamoto M; Roume J; Couderc S; Vialard F; Hillion Y; Ville Y
Prenat Diagn; 2006 Apr; 26(4):369-72. PubMed ID: 16566042
[TBL] [Abstract][Full Text] [Related]
19. Familial nuchal cystic hygroma without fetal effects: Genetic counselling and further evidence for an autosomal recessive subtype.
Bianca S; Bartoloni G; Boemi G; Barrano B; Barone C; Cataliotti A; Indaco L; Ettore G
Congenit Anom (Kyoto); 2010 Jun; 50(2):139-40. PubMed ID: 20156236
[No Abstract] [Full Text] [Related]
20. Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in a fetus with major congenital anomalies.
Hou WC; Chen CP; Hwang KS; Chen YC; Lai YJ; Tien CY; Su HY
Taiwan J Obstet Gynecol; 2014 Dec; 53(4):602-5. PubMed ID: 25510709
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
