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Micheal S 12

Showing records 1 to 12 | Display all abstracts from Micheal S

69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0159259

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Micheal S
PLoS ONE 2016; 11: e0160016

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69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0159259

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Siddiqui SN
PLoS ONE 2016; 11: e0160016

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69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Zafar SN
PLoS ONE 2016; 11: e0159259

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Zafar SN
PLoS ONE 2016; 11: e0160016

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69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Iqbal A
PLoS ONE 2016; 11: e0159259

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Villanueva-Mendoza C; Cortés-González V
PLoS ONE 2016; 11: e0160016

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69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
Khan MI
PLoS ONE 2016; 11: e0159259

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
Khan MI
PLoS ONE 2016; 11: e0160016

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69321 Identification of Novel Variants in LTBP2 and PXDN Using Whole-Exome Sequencing in Developmental and Congenital Glaucoma
den Hollander AI
PLoS ONE 2016; 11: e0159259

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69406 A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
den Hollander AI
PLoS ONE 2016; 11: e0160016

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