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WGC-2021

9.1.3 Syndromes of Axenfeld, Rieger, Peters, aniridia (8)

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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, aniridia
84752 Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Gauthier AC
Experimental Eye Research 2020; 190: 107893
84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Nandeesh BN
Neuropathology 2020; 40: 93-98
85093 Novel Ocular and Inner Ear Anomalies in a Patient with Myhre Syndrome
Gürsoy S; Hazan F
Molecular syndromology 2020; 10: 339-343
84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Bindu PS
Neuropathology 2020; 40: 93-98
84752 Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss
Wiggs JL
Experimental Eye Research 2020; 190: 107893
84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Narayanappa G
Neuropathology 2020; 40: 93-98
85093 Novel Ocular and Inner Ear Anomalies in a Patient with Myhre Syndrome
Öztürk T; Ateş H
Molecular syndromology 2020; 10: 339-343
84689 Cerebral small vessel disease with hemorrhagic stroke related to COL4A1 mutation: A case report
Chickabasaviah Yasha T; Mahadevan A; Kulanthaivelu K; Santosh V
Neuropathology 2020; 40: 93-98

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