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.
148 related articles for article (PubMed ID: 6502411)
1. Role of the neural crest in anterior segment development and disease. Beauchamp GR; Knepper PA J Pediatr Ophthalmol Strabismus; 1984; 21(6):209-14. PubMed ID: 6502411 [TBL] [Abstract][Full Text] [Related]
2. Neurocristopathies: Enigmatic Appearances of Neural Crest Cell-derived Abnormalities. Sato TS; Handa A; Priya S; Watal P; Becker RM; Sato Y Radiographics; 2019; 39(7):2085-2102. PubMed ID: 31697622 [TBL] [Abstract][Full Text] [Related]
3. The 6p25 deletion syndrome: An update on a rare neurocristopathy. de Vos IJ; Stegmann AP; Webers CA; Stumpel CT Ophthalmic Genet; 2017; 38(2):101-107. PubMed ID: 27070436 [TBL] [Abstract][Full Text] [Related]
4. Relationship between neural crest cell specification and rare ocular diseases. Akula M; Park JW; West-Mays JA J Neurosci Res; 2019 Jan; 97(1):7-15. PubMed ID: 29660784 [TBL] [Abstract][Full Text] [Related]
6. Differences in neural crest sensitivity to ethanol account for the infrequency of anterior segment defects in the eye compared with craniofacial anomalies in a zebrafish model of fetal alcohol syndrome. Eason J; Williams AL; Chawla B; Apsey C; Bohnsack BL Birth Defects Res; 2017 Sep; 109(15):1212-1227. PubMed ID: 28681995 [TBL] [Abstract][Full Text] [Related]
7. Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma. Martino VB; Sabljic T; Deschamps P; Green RM; Akula M; Peacock E; Ball A; Williams T; West-Mays JA Dis Model Mech; 2016 Aug; 9(8):849-61. PubMed ID: 27483349 [TBL] [Abstract][Full Text] [Related]
14. Neural crest derivatives in ocular development: discerning the eye of the storm. Williams AL; Bohnsack BL Birth Defects Res C Embryo Today; 2015 Jun; 105(2):87-95. PubMed ID: 26043871 [TBL] [Abstract][Full Text] [Related]
15. Axenfeld anomaly in association with hypomelanosis of Ito. Flaherty MP; Padilla CD; Sillence DO Ophthalmic Paediatr Genet; 1991 Mar; 12(1):23-30. PubMed ID: 1881652 [TBL] [Abstract][Full Text] [Related]
16. Severe bilateral ocular features in Goldenhar's syndrome. Mc Alister JC; Olver JM; Hatter T J Pediatr Ophthalmol Strabismus; 2001; 38(1):44-6. PubMed ID: 11201919 [No Abstract] [Full Text] [Related]
17. Multiple accessory tragi as a clue to the diagnosis of the oculo-auriculo-vertebral (Goldenhar) syndrome. Miller TD; Metry D J Am Acad Dermatol; 2004 Feb; 50(2 Suppl):S11-3. PubMed ID: 14726857 [TBL] [Abstract][Full Text] [Related]
18. A patient with median cleft face anomaly and bilateral Goldenhar anomaly. Musarella MA; Young ID Am J Med Genet Suppl; 1986; 2():135-41. PubMed ID: 3146283 [TBL] [Abstract][Full Text] [Related]
19. Molecular genetics of Axenfeld-Rieger malformations. Lines MA; Kozlowski K; Walter MA Hum Mol Genet; 2002 May; 11(10):1177-84. PubMed ID: 12015277 [TBL] [Abstract][Full Text] [Related]
20. Anterior segment anomalies of the eye associated with multiple skeletal abnormalities and early lethality: confirmation of an autosomal recessive syndrome. al-Gazali LI; Bakir M; Sadaghatian MR; Nath R; Haas D Clin Dysmorphol; 1999 Apr; 8(2):87-92. PubMed ID: 10319196 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]