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A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene.
Am J Hum Genet. 1991 Dec;49(6):1256-62.
Am J Hum Genet. 1991.
PMID: 1720926
Free PMC article.
Carbonic anhydrase II deficiency syndrome in a Belgian family is caused by a point mutation at an invariant histidine residue (107 His----Tyr): complete structure of the normal human CA II gene.
Venta PJ, Welty RJ, Johnson TM, Sly WS, Tashian RE.
Venta PJ, et al.
Am J Hum Genet. 1991 Nov;49(5):1082-90.
Am J Hum Genet. 1991.
PMID: 1928091
Free PMC article.
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