久久久www成人免费毛片麻豆,成人免费在线观看毛片,9久久免费国产精品特黄国产蜜桃,国产精品日韩欧美一区二区视频,亚州av无码乱码精品国产,欧美日韩视频综合一区无弹窗,天堂中文字幕av成人网站

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