These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
154 related articles for article (PubMed ID: 24592072)
1. Prenatal diagnosis of frontonasal dysplasia with anterior encephalocele. Esmer AÇ; Kalelioğlu I; Kayserili H; Yüksel A; Has R J Turk Ger Gynecol Assoc; 2013; 14(1):50-2. PubMed ID: 24592072 [TBL] [Abstract][Full Text] [Related]
2. [A new prenatal diagnosis case of frontonasal dysplasia]. Guigue V; Martin A; Mangin M; Arbez-Gindre F; Labenne E; Olivier-Faivre L; Ramanah R; Riethmuller D J Gynecol Obstet Biol Reprod (Paris); 2011 Sep; 40(5):476-80. PubMed ID: 21388753 [TBL] [Abstract][Full Text] [Related]
3. Clinical delineation of a subtype of frontonasal dysplasia with creased nasal ridge and upper limb anomalies: Report of six unrelated patients. Lehalle D; Altunoglu U; Bruel AL; Arnaud E; Blanchet P; Choi JW; Désir J; Kiliç E; Lederer D; Pinson L; Thauvin-Robinet C; Singer A; Thevenon J; Callier P; Kayserili H; Faivre L Am J Med Genet A; 2017 Dec; 173(12):3136-3142. PubMed ID: 29136349 [TBL] [Abstract][Full Text] [Related]
4. Prenatal diagnosis of frontonasal dysplasia associated with bilateral periventricular nodular heterotopia. Recio-Rodríguez M; Fernández-Mayoralas DM; Fernández-Jaén A; Fernández-Perrone AL; Cano-Alonso R; Jiménez-de-La-Peña M J Child Neurol; 2014 Oct; 29(10):NP122-6. PubMed ID: 24196422 [TBL] [Abstract][Full Text] [Related]
5. Prenatal diagnosis of isolated frontonasal dysplasia: A case report. Lourenço C; Godinho C; Marinho M; Melo M; Nogueira R; Valente F J Clin Ultrasound; 2021 Feb; 49(2):145-148. PubMed ID: 32374429 [TBL] [Abstract][Full Text] [Related]
6. Prenatal diagnosis of a severe form of frontonasal dysplasia with severe limb anomalies, hydrocephaly, a hypoplastic corpus callosum, and a ventricular septal defect using 3D ultrasound: a case report and literature review. Guo C; Zhang T; Ma Y; Yue S; Sun L BMC Pregnancy Childbirth; 2024 Jun; 24(1):420. PubMed ID: 38858685 [TBL] [Abstract][Full Text] [Related]
7. Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs, and thanatophoric dysplasia type II. Chen CP; Chang TY; Lin MH; Chern SR; Su JW; Wang W Taiwan J Obstet Gynecol; 2013 Sep; 52(3):420-5. PubMed ID: 24075385 [TBL] [Abstract][Full Text] [Related]