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X-linked ocular albinism and sensorineural deafness: linkage to Xp22.3.
Genomics. 1993 Nov;18(2):444-5. doi: 10.1006/geno.1993.1495.
Genomics. 1993.
PMID: 8288253
Retinitis pigmentosa, AD type I: exclusion of linkage to D3S47 (C17) in a large South African family of British origin.
Greenberg J, Babaya M, Ramesar R, Beighton P.
Greenberg J, et al. Among authors: babaya m.
Clin Genet. 1992 Jun;41(6):322-5. doi: 10.1111/j.1399-0004.1992.tb03406.x.
Clin Genet. 1992.
PMID: 1623630
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Molecular investigation of familial Beckwith-Wiedemann syndrome: a model for paternal imprinting.
Ramesar R, Babaya M, Viljoen D.
Ramesar R, et al. Among authors: babaya m.
Eur J Hum Genet. 1993;1(2):109-13. doi: 10.1159/000472397.
Eur J Hum Genet. 1993.
PMID: 8055321
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