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Xu M 11

Showing records 1 to 11 | Display all abstracts from Xu M

96283 Compound heterozygous mutations in the LTBP2 gene associated with microspherophakia in a Chinese patient: a case report and literature review
Xu M
BMC Medical Genomics 2021; 14: 227

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96390 A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review
Li K
BMC Medical Genomics 2021; 14: 255

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96107 A novel mutation in gene causes primary angle-closure glaucoma
Xu M
Aging 2021; 13: 23338-23347

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96390 A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review
Tang M
BMC Medical Genomics 2021; 14: 255

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96107 A novel mutation in gene causes primary angle-closure glaucoma
Yang J
Aging 2021; 13: 23338-23347

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96283 Compound heterozygous mutations in the LTBP2 gene associated with microspherophakia in a Chinese patient: a case report and literature review
Li K; He W
BMC Medical Genomics 2021; 14: 227

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96107 A novel mutation in gene causes primary angle-closure glaucoma
Sun J
Aging 2021; 13: 23338-23347

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96390 A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review
Xu M
BMC Medical Genomics 2021; 14: 255

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96107 A novel mutation in gene causes primary angle-closure glaucoma
Xing X
Aging 2021; 13: 23338-23347

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96390 A novel missense mutation of FOXC1 in an Axenfeld-Rieger syndrome patient with a congenital atrial septal defect and sublingual cyst: a case report and literature review
Yu Y
BMC Medical Genomics 2021; 14: 255

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96107 A novel mutation in gene causes primary angle-closure glaucoma
Liu Z; Liu T
Aging 2021; 13: 23338-23347

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