121 related articles for article (PubMed ID: 3316692)
1. The ultrasonic detection of Apert syndrome.
Hill LM; Thomas ML; Peterson CS
J Ultrasound Med; 1987 Oct; 6(10):601-4. PubMed ID: 3316692
[No Abstract] [Full Text] [Related]
2. Prenatal molecular diagnosis for Apert syndrome.
Osada H; Ishii J; Sekiya S
Int J Gynaecol Obstet; 1996 Nov; 55(2):171-2. PubMed ID: 8961003
[No Abstract] [Full Text] [Related]
3. Apert syndrome associated with increased fetal nuchal translucency.
Aleem S; Howarth ES
Prenat Diagn; 2005 Nov; 25(11):1066-7. PubMed ID: 16302163
[No Abstract] [Full Text] [Related]
4. Apert syndrome and fetal hydrocephaly.
Kim H; Uppal V; Wallach R
Hum Genet; 1986 May; 73(1):93-5. PubMed ID: 3519431
[TBL] [Abstract][Full Text] [Related]
5. Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18.
Chen CP; Su YN; Hsu CY; Ling PY; Tsai FJ; Chern SR; Wu PC; Chen HE; Wang W
Taiwan J Obstet Gynecol; 2010 Mar; 49(1):129-32. PubMed ID: 20466312
[No Abstract] [Full Text] [Related]
6. Diaphragmatic hernia as an early ultrasound manifestation of Apert syndrome.
Kosiński P; Luterek K; Wielgoś M
Ginekol Pol; 2016; 87(12):830. PubMed ID: 28098935
[TBL] [Abstract][Full Text] [Related]
7. Detection of the S252W mutation in fibroblast growth factor receptor 2 (FGFR2) in fetal DNA from maternal plasma in a pregnancy affected by Apert syndrome.
Au PK; Kwok YK; Leung KY; Tang LY; Tang MH; Lau ET
Prenat Diagn; 2011 Feb; 31(2):218-20. PubMed ID: 21268044
[No Abstract] [Full Text] [Related]
8. Prenatal fetoscopic diagnosis of the Apert syndrome.
Leonard CO; Daikoku NH; Winn K
Am J Med Genet; 1982 Jan; 11(1):5-9. PubMed ID: 7065003
[TBL] [Abstract][Full Text] [Related]
9. Ultrasound detection of Apert syndrome: a case report and literature review.
Kaufmann K; Baldinger S; Pratt L
Am J Perinatol; 1997 Aug; 14(7):427-30. PubMed ID: 9263565
[TBL] [Abstract][Full Text] [Related]
10. Prenatal diagnosis of apert syndrome with cloverleaf skull deformity using ultrasound, fetal magnetic resonance imaging and genetic analysis.
Weber B; Schwabegger AH; Vodopiutz J; Janecke AR; Forstner R; Steiner H
Fetal Diagn Ther; 2010; 27(1):51-6. PubMed ID: 19940464
[TBL] [Abstract][Full Text] [Related]
11. Apert syndrome: what prenatal radiographic findings should prompt its consideration?
Quintero-Rivera F; Robson CD; Reiss RE; Levine D; Benson C; Mulliken JB; Kimonis VE
Prenat Diagn; 2006 Oct; 26(10):966-72. PubMed ID: 16906598
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis of Apert syndrome.
Chang CC; Tsai FJ; Tsai HD; Tsai CH; Hseih YY; Lee CC; Yang TC; Wu JY
Prenat Diagn; 1998 Jun; 18(6):621-5. PubMed ID: 9664610
[TBL] [Abstract][Full Text] [Related]
13. Molecular diagnosis of Apert syndrome in Chinese patients.
Tsai FJ; Tsai CH; Peng CT; Lin SP; Hwu WL; Wang TR; Lee CC; Wu JY
Acta Paediatr Taiwan; 1999; 40(1):31-3. PubMed ID: 10910582
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biology.
Mahieu-Caputo D; Sonigo P; Amiel J; Simon I; Aubry MC; Lemerrer M; Delezoïde AL; Gigarel N; Dommergues M; Dumez Y
Fetal Diagn Ther; 2001; 16(1):10-2. PubMed ID: 11125244
[TBL] [Abstract][Full Text] [Related]
15. Progressive development of sonographic features in prenatal diagnosis of Apert syndrome--case report and literature review.
Respondek-Liberska M; Smigiel R; Zielinski A; Sasiadek MM
Ginekol Pol; 2010 Dec; 81(12):935-9. PubMed ID: 21391441
[TBL] [Abstract][Full Text] [Related]
16. Application of the three-dimensional maximum mode in prenatal diagnosis of Apert syndrome.
Esser T; Rogalla P; Bamberg C; Kalache KD
Am J Obstet Gynecol; 2005 Nov; 193(5):1743-5. PubMed ID: 16260220
[TBL] [Abstract][Full Text] [Related]
17. Fetal macrosomia as an important indicator of fetal malformation syndrome: ultrasonic findings of two cases.
Wouters EJ; Pley EA; de Jong PA
Eur J Obstet Gynecol Reprod Biol; 1989 Sep; 32(3):253-7. PubMed ID: 2676641
[TBL] [Abstract][Full Text] [Related]
18. Prenatal ultrasonic diagnosis of short rib polydactyly syndrome, type I. A case report.
Meizner I; Bar-Ziv J
J Reprod Med; 1989 Sep; 34(9):668-72. PubMed ID: 2681751
[TBL] [Abstract][Full Text] [Related]
19. Prenatal ultrasonic detection of bilateral hydrocele.
Hurwitz A; Yagel S; Abramov M; Adoni A
Am J Perinatol; 1984 Jan; 1(2):195. PubMed ID: 6394014
[No Abstract] [Full Text] [Related]
20. Detection of fetal malformations with ultrasonic B-scans.
Filly RA
Birth Defects Orig Artic Ser; 1979; 15(5A):45-9. PubMed ID: 508919
[No Abstract] [Full Text] [Related]
[Next] [New Search]
