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Gene 28
Showing records 1 to 25 | Display all abstracts in Gene61138 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
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Yang Y
Gene 2015; 571: 188-193
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma
Bashir R
Gene 2015; 570: 295-298
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Zhu X
Gene 2015; 571: 142-144
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma
Tahir H
Gene 2015; 570: 295-298
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Dai FR
Gene 2015; 571: 142-144
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Shi Y
Gene 2015; 571: 188-193
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
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Huang X
Gene 2015; 571: 188-193
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Wang J
Gene 2015; 571: 142-144
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Popp B
Gene 2015; 568: 76-80
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma
Yousaf K
Gene 2015; 570: 295-298
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Li X
Gene 2015; 571: 188-193
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Zhang Y
Gene 2015; 571: 142-144
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Sticht H
Gene 2015; 568: 76-80
61587 Homozygous p.G61E mutation in a consanguineous Pakistani family with co-existence of juvenile-onset open angle glaucoma and primary congenital glaucoma
Naz S
Gene 2015; 570: 295-298
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
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Ye Z
Gene 2015; 571: 188-193
61558 Novel BCOR mutation in a boy with Lenz microphthalmia/oculo-facio-cardio-dental (OFCD) syndrome
Tan ZP
Gene 2015; 571: 142-144
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Shuai P
Gene 2015; 571: 188-193
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
Gene 2015; 568: 76-80
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Qu C
Gene 2015; 571: 188-193
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Penco S
Gene 2015; 568: 76-80
61351 Identification of a novel MYOC mutation in a Chinese family with primary open-angle glaucoma
Chen R
Gene 2015; 571: 188-193
61138 Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma
Schlötzer-Schrehardt U
Gene 2015; 568: 76-80
