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Firasat S 7
Showing records 1 to 7 | Display all abstracts from Firasat S106644 Screening of high-risk deleterious missense variations in the gene implicated in the pathogenesis of primary congenital glaucoma: A comprehensive approach
Shahid M; Shahid M
PeerJ 2022; 10: e14132
105740 Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma
Tehreem R; Arooj A
PLoS ONE 2022; 17: e0274335
106644 Screening of high-risk deleterious missense variations in the gene implicated in the pathogenesis of primary congenital glaucoma: A comprehensive approach
Azfaralariff A; Tufail M
PeerJ 2022; 10: e14132
105740 Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma
Siddiqui SN; Naz S
PLoS ONE 2022; 17: e0274335
106644 Screening of high-risk deleterious missense variations in the gene implicated in the pathogenesis of primary congenital glaucoma: A comprehensive approach
Hussain Khan N; Abdulkareem Najm A
PeerJ 2022; 10: e14132
105740 Mutation screening of the CYP1B1 gene reveals thirteen novel disease-causing variants in consanguineous Pakistani families causing primary congenital glaucoma
Afshan K; Firasat S
PLoS ONE 2022; 17: e0274335
106644 Screening of high-risk deleterious missense variations in the gene implicated in the pathogenesis of primary congenital glaucoma: A comprehensive approach
Firasat S; Zubair M; Fazry S; Law D
PeerJ 2022; 10: e14132
