115 related articles for article (PubMed ID: 8750304)
1. The ultrasonic detection of an isolated craniosynostosis.
van der Ham LI; Cohen-Overbeek TE; Paz y Geuze HD; Vermeij-Keers C
Prenat Diagn; 1995 Dec; 15(12):1189-92. PubMed ID: 8750304
[TBL] [Abstract][Full Text] [Related]
2. Isolated craniosynostosis: prenatal ultrasound of scaphocephaly with polyhydramnios.
Huang HW; Lin H; Chang SY; Hsu YH; Hsu TY
Chang Gung Med J; 2001 Dec; 24(12):816-9. PubMed ID: 11858399
[TBL] [Abstract][Full Text] [Related]
3. Prenatal sonographic appearance of Beare-Stevenson cutis gyrata syndrome: two- and three-dimensional ultrasonographic findings.
Hsu TY; Chang SY; Wang TJ; Ou CY; Chen ZH; Hsu PH
Prenat Diagn; 2001 Aug; 21(8):665-7. PubMed ID: 11536267
[TBL] [Abstract][Full Text] [Related]
4. The Brain Shadowing Sign: A Clue Finding for Early Suspicion of Craniosynostosis?
Dall'Asta A; Paramasivam G; Lees C; Ghi T; Frusca T
Fetal Diagn Ther; 2019; 45(5):357-360. PubMed ID: 30138932
[TBL] [Abstract][Full Text] [Related]
5. Prenatal ultrasound parameters in single-suture craniosynostosis.
Cornelissen MJ; Apon I; van der Meulen JJNM; Groenenberg IAL; Kraan-van der Est MN; Mathijssen IMJ; Bonsel GJ; Cohen-Overbeek TE
J Matern Fetal Neonatal Med; 2018 Aug; 31(15):2050-2057. PubMed ID: 28553772
[TBL] [Abstract][Full Text] [Related]
6. Prenatal identification of a G338E mutation in FGFR2 in a fetus without sonographic appearance of craniosynostosis.
Chen CP; Chern SR; Lin SP; Wang W; Tsai FJ
Prenat Diagn; 2003 Feb; 23(2):175-6. PubMed ID: 12575031
[No Abstract] [Full Text] [Related]
7. Prenatal diagnosis of craniosynostosis: sonographic features of Muenke syndrome.
Shaw A; Petersen OB; Chitty LS
J Obstet Gynaecol; 2011 Nov; 31(8):770-1. PubMed ID: 22085076
[No Abstract] [Full Text] [Related]
8. Polyhydramnios as a prenatal symptom of the digeorge/velo-cardio-facial syndrome.
Devriendt K; Van Schoubroeck D; Eyskens B; Vantrappen G; Swillen A; Gewillig M; Dumoulin M; Moerman P; Vandenberghe K; Fryns JP
Prenat Diagn; 1998 Jan; 18(1):68-72. PubMed ID: 9483643
[TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of monosomy 17p (17p13.3-->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly, and Miller-Dieker lissencephaly syndrome in a fetus.
Lin CY; Chen CP; Liau CL; Su PH; Tsao TF; Chang TY; Wang W
Taiwan J Obstet Gynecol; 2009 Dec; 48(4):408-11. PubMed ID: 20045764
[TBL] [Abstract][Full Text] [Related]
10. [The polyhydramnios symptom: analysis of 56 cases].
Yaman C; Arzt W; Tulzer G; Tews G
Geburtshilfe Frauenheilkd; 1996 Jun; 56(6):287-90. PubMed ID: 8766485
[TBL] [Abstract][Full Text] [Related]
11. Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature.
Tonni G; Panteghini M; Rossi A; Baldi M; Magnani C; Ferrari B; Lituania M
Arch Gynecol Obstet; 2011 Apr; 283(4):909-16. PubMed ID: 20811900
[TBL] [Abstract][Full Text] [Related]
12. Rapid detection of de novo P253R mutation in FGFR2 using uncultured amniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst, and Apert syndrome.
Chen CP; Su YN; Chang TY; Chern SR; Chen CY; Su JW; Wang W
Taiwan J Obstet Gynecol; 2013 Jun; 52(2):273-7. PubMed ID: 23915865
[TBL] [Abstract][Full Text] [Related]
13. Prenatal sonographic appearance of asymmetric craniosynostosis: a case report.
Meilstrup JW; Botti JJ; MacKay DR; Johnson DL
J Ultrasound Med; 1995 Apr; 14(4):307-10. PubMed ID: 7602691
[No Abstract] [Full Text] [Related]
14. Diagnosis of 9q22.3 microdeletion syndrome in utero following identification of craniosynostosis, overgrowth, and skeletal anomalies.
Reichert SC; Zelley K; Nichols KE; Eberhard M; Zackai EH; Martinez-Poyer J
Am J Med Genet A; 2015 Apr; 167A(4):862-5. PubMed ID: 25706929
[TBL] [Abstract][Full Text] [Related]
15. [Craniosynostosis: is prenatal diagnosis possible?].
Nuzzi FM; Botti C; Morini P; Daino A; Pardini A
Minerva Ginecol; 1998 Dec; 50(12):549-52. PubMed ID: 10069170
[TBL] [Abstract][Full Text] [Related]
16. Ultrasound diagnosis of craniosynostosis.
Miller C; Losken HW; Towbin R; Bowen A; Mooney MP; Towbin A; Faix RS
Cleft Palate Craniofac J; 2002 Jan; 39(1):73-80. PubMed ID: 11772173
[TBL] [Abstract][Full Text] [Related]
17. Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3).
Chen CP; Lin YH; Au HK; Su YN; Hsu CY; Liu YP; Wu PC; Chern SR; Chen YT; Chen LF; Hsieh AH; Wang W
Taiwan J Obstet Gynecol; 2011 Sep; 50(3):359-65. PubMed ID: 22030053
[TBL] [Abstract][Full Text] [Related]
18. Do multiple measurements employing different ultrasonic techniques improve the accuracy of amniotic fluid volume assessment?
Magann EF; Chauhan SP; Whitworth NS; Klausen JH; Saltzman AK; Morrison JC
Aust N Z J Obstet Gynaecol; 1998 May; 38(2):172-5. PubMed ID: 9653854
[TBL] [Abstract][Full Text] [Related]
19. A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome).
Tejada MI; Uribarren A; Briones P; Vilaseca MA
Prenat Diagn; 1992 Jun; 12(6):529-34. PubMed ID: 1513756
[TBL] [Abstract][Full Text] [Related]
20. Diagnostic accuracy of ultrasonic examination in suspected craniosynostosis among infants.
Alizadeh H; Najmi N; Mehdizade M; Najmi N
Indian Pediatr; 2013 Jan; 50(1):148-50. PubMed ID: 23396787
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
