154 related articles for article (PubMed ID: 19127784)
1. Prenatal ultrasonographic findings in "trisomy 13".
Pitukkijronnakorn S; Promsonthi P; Panburana P; Rangsiprakarn R; Chittacharoen A
J Med Assoc Thai; 2008 Nov; 91(11):1651-5. PubMed ID: 19127784
[TBL] [Abstract][Full Text] [Related]
2. Trisomy 13 syndrome: prenatal US findings in a review of 33 cases.
Lehman CD; Nyberg DA; Winter TC; Kapur RP; Resta RG; Luthy DA
Radiology; 1995 Jan; 194(1):217-22. PubMed ID: 7997556
[TBL] [Abstract][Full Text] [Related]
3. [Study on key techniques and intervention in reducing birth defects].
Zhu BS; Su J; Lu XH; He J; Zhu S; Jiao CX; Zhang JM; Tang XH; Tao Y; Lin KP; Chen H; Li SY
Zhonghua Fu Chan Ke Za Zhi; 2011 Sep; 46(9):658-63. PubMed ID: 22176989
[TBL] [Abstract][Full Text] [Related]
4. Sonographic screening for trisomy 13 at 11 to 13(+6) weeks of gestation.
Papageorghiou AT; Avgidou K; Spencer K; Nix B; Nicolaides KH
Am J Obstet Gynecol; 2006 Feb; 194(2):397-401. PubMed ID: 16458636
[TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of trisomy 13: analysis of 28 cases.
Papp C; Beke A; Ban Z; Szigeti Z; Toth-Pal E; Papp Z
J Ultrasound Med; 2006 Apr; 25(4):429-35. PubMed ID: 16567430
[TBL] [Abstract][Full Text] [Related]
6. Prenatal ultrasound findings in complete trisomy 9.
Sepulveda W; Wimalasundera RC; Taylor MJ; Blunt S; Be C; De La Fuente S
Ultrasound Obstet Gynecol; 2003 Nov; 22(5):479-83. PubMed ID: 14618660
[TBL] [Abstract][Full Text] [Related]
7. [The prenatal detection of trisomy 13, 18, and 21: comparison of the advanced first trimester screening (AFS) with the first trimester screening according to Nicolaides].
Hörmansdörfer C; Schmidt P; Hillemanns P; Scharf A
Z Geburtshilfe Neonatol; 2007 Dec; 211(6):243-9. PubMed ID: 18176905
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of iniencephaly and alobar holoprosencephaly with trisomy 13 mosaicism: a case report.
Phadke SR; Thakur S
Prenat Diagn; 2002 Dec; 22(13):1240-1. PubMed ID: 12478643
[No Abstract] [Full Text] [Related]
9. Correlation of prenatal ultrasound diagnosis and pathologic findings in fetuses with trisomy 13.
Szigeti Z; Csapó Z; Joó JG; Pete B; Papp Z; Papp C
Prenat Diagn; 2006 Dec; 26(13):1262-6. PubMed ID: 17099926
[TBL] [Abstract][Full Text] [Related]
10. Holoprosencephaly: examples of clinical variability and etiologic heterogeneity.
Corsello G; Buttitta P; Cammarata M; Lo Presti A; Maresi E; Zumpani L; Giuffrè L
Am J Med Genet; 1990 Oct; 37(2):244-9. PubMed ID: 2147361
[TBL] [Abstract][Full Text] [Related]
11. Holoprosencephaly-polydactyly (pseudotrisomy 13) syndrome: case report and diagnostic criteria.
Sergi C; Gekas J; Kamnasaran D
Fetal Pediatr Pathol; 2012 Oct; 31(5):315-8. PubMed ID: 22432933
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of partial trisomy 3p(3p23-->pter) and monosomy 7q(7q36-->qter) in a fetus with microcephaly alobar holoprosencephaly and cyclopia.
Chen CP; Devriendt K; Lee CC; Chen WL; Wang W; Wang TY
Prenat Diagn; 1999 Oct; 19(10):986-9. PubMed ID: 10521829
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of trisomy 4p: a new locus for holoprosencephaly?
Karmous-Benailly H; Tabet AC; Thaly A; Dupuy O; Huten Y; Luton D; Baumann C; Delezoide AL
Prenat Diagn; 2005 Mar; 25(3):193-7. PubMed ID: 15791668
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of de novo partial trisomy 13q (13q22 --> qter) and partial monosomy 8p (8p23.3 --> pter) associated with holoprosencephaly, premaxillary agenesis, hexadactyly, and a hypoplastic left heart.
Chen CP; Chern SR; Hsu CY; Lee CC; Lee MS; Wang W
Prenat Diagn; 2005 Apr; 25(4):334-6. PubMed ID: 15849788
[No Abstract] [Full Text] [Related]
15. [Prenatal diagnosis of trisomy 13 and trisomy 18: the experience of Assaf-Harofe Medical Center].
Naor Dovev M; Maymon R; Keidar R; Reish O; Melcer Y; Vaknin Z
Harefuah; 2014 Aug; 153(8):453-7, 499, 498. PubMed ID: 25286634
[TBL] [Abstract][Full Text] [Related]
16. Chromosomal abnormalities in fetuses with open neural tube defects: prenatal identification with ultrasound.
Sepulveda W; Corral E; Ayala C; Be C; Gutierrez J; Vasquez P
Ultrasound Obstet Gynecol; 2004 Apr; 23(4):352-6. PubMed ID: 15065184
[TBL] [Abstract][Full Text] [Related]
17. Prenatal foetal diagnosis of partial trisomy 3q and monosomy 13p due to a maternal balanced rearrangement.
Pires A; Ramos L; Venâncio M; Rei AI; Castedo S; Saraiva J
Prenat Diagn; 2005 Apr; 25(4):292-5. PubMed ID: 15849779
[TBL] [Abstract][Full Text] [Related]
18. Cyclopia, proboscis and alobar holoprosencephaly representative for trisomy 13.
Bozkurt O; Kanmaz HG; Sahin S; Canpolat FE; Uras N; Oguz SS; Dilmen U
Genet Couns; 2014; 25(3):349-51. PubMed ID: 25365860
[No Abstract] [Full Text] [Related]
19. Antenatally detectable markers for the diagnosis of autosomally trisomic fetuses in at-risk pregnancies.
Salihu HM; Boos R; Schmidt W
Am J Perinatol; 1997 May; 14(5):257-61. PubMed ID: 9259939
[TBL] [Abstract][Full Text] [Related]
20. Increased fetal nuchal translucency as a sole clue in the prenatal diagnosis of a fetus with trisomy 13.
Ki KD; Kim SR; Lee WI
Fetal Diagn Ther; 2009; 26(1):54-6. PubMed ID: 19816033
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
