99精品久久99久久久久,亚洲国产成人精品无码一区二区,国产精品亚洲综合色区韩国,久久精品第一国产久精国产宅男66,亚洲国产日韩欧美一区二区三区,久久久久久精品免费无码无,国产中年熟女高潮大集合,亚洲AV无码成H在线观看

Musarella MA, et al. Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis. Am. J. Hum. Genet. 43: 484-494, 1988. PubMed: 2902787

Francke U, et al. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: Molecular genetic evidence for deletions. Am. J. Hum. Genet. 40: 212-227, 1987. PubMed: 2883886

Davies KE, et al. Gene for OTC: Characterization and linkage to Duchenne muscular dystrophy. Nucleic Acids Res. 13: 155-165, 1985. PubMed: 3839070

Pembrey ME, et al. Prenatal diagnosis of ornithine carbamoyl transferase deficiency using a gene specific probe. J. Med. Genet. 22: 462-465, 1985. PubMed: 3001312