advertisement
9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (12)
Showing records 1 to 12
Display all abstracts in classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia
Search within classification 9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia61040 Neural crest derivatives in ocular development: Discerning the eye of the storm
Williams AL
Birth Defects Research Part C-Embryo Today: Reviews 2015; 105: 87-95
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Pasutto F
Gene 2015; 568: 76-80
61494 A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings
Yang HJ
Korean Journal of Ophthalmology 2015; 29: 249-255
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Mauri L
Gene 2015; 568: 76-80
61494 A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings
Lee YK
Korean Journal of Ophthalmology 2015; 29: 249-255
61040 Neural crest derivatives in ocular development: Discerning the eye of the storm
Bohnsack BL
Birth Defects Research Part C-Embryo Today: Reviews 2015; 105: 87-95
61494 A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings
Joo CK
Korean Journal of Ophthalmology 2015; 29: 249-255
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Popp B; Sticht H
Gene 2015; 568: 76-80
61494 A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings
Moon JI; Mok JW
Korean Journal of Ophthalmology 2015; 29: 249-255
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Ekici A
Gene 2015; 568: 76-80
61494 A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings
Park MH
Korean Journal of Ophthalmology 2015; 29: 249-255
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Piozzi E; Bonfante A; Penco S; Schlötzer-Schrehardt U; Reis A
Gene 2015; 568: 76-80
