A Second Locus ( GLC3B ) for Primary Congenital Glaucoma (Buphthalmos) Maps to the 1p36 Region

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Human Molecular Genetics, Vol. 5, Iss. 8, 1996-01 ,pp. : 1199-1203

Oxford University Press

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Identification of Three Different Truncating Mutations in Cytochrome P4501B1 ( CYP1B1 ) as the Principal Cause of Primary Congenital Glaucoma (Buphthalmos) in Families Linked to the GLC3A Locus on Chromosome 2p21

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Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 641-647

Oxford University Press

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Coinheritance of Chromosomes 3 and 11 in the Patients with Autosomal Recessive Polycythemia from Chuvachia

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Russian Journal of Genetics, Vol. 41, Iss. 9, 2005-09 ,pp. : 1035-1039

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Autosomal Recessive Non-Syndromic Deafness Locus (DFNB8) Maps on Chromosome 21Q22 in a Large Consanguineous Kindred from Pakistan

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Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 165-168

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Localization of A Novel Autosomal Recessive Non-Syndromic Hearing Impairment Locus (DFNB38) to 6q26-q27 in a Consanguineous Kindred from Pakistan

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