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BMC Medical Genomics 6
Showing records 1 to 6 | Display all abstracts in BMC Medical Genomics96283 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
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
96283 Compound heterozygous mutations in the LTBP2 gene associated with microspherophakia in a Chinese patient: a case report and literature review
Li K
BMC Medical Genomics 2021; 14: 227
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
96283 Compound heterozygous mutations in the LTBP2 gene associated with microspherophakia in a Chinese patient: a case report and literature review
He W
BMC Medical Genomics 2021; 14: 227
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; Yu Y
BMC Medical Genomics 2021; 14: 255
