Author:
Chelly J.,Marlhens F.,Dutrillaux B.,Van Ommen G. J.,Lambert M.,Haioun B.,Boissinot G.,Fardeau M.,Kaplan J. -C.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference30 articles.
1. Aldridge, J, Kunkel LM, Bruns G, Tantravahi U, Lalande M, Brenster T, Moreau E, Wilson M, Bromley W, Rodrick T, Latt SA (1984) A strategy to reveal high frequence RFLPs along the human X chromosome. Am J Hum Genet 36:546?564
2. Bakker E, Hofker MH, Goor N, Mandel JL, Wrogemann K, Davies KE, Kunkel LM, Willard HF, Fenton WA, Sankuyl L, Majoor-Krakauer D, Essen AJ van, Jahoda JMG, Sachs ES, Van Ommen GJB, Pearson PL (1985) Prenatal diagnosis and carrier detection of Duchenne muscular dystrophy with closely linked RFLPs. Lancet II:655?658
3. Bartley JA, Miller DK, Hayford JT, McCabe ERB (1982) The concordance of X-linked glycerol kinase deficiency with X-linked adrenal hypoplasia in two families. Lancet II:733
4. Bartley JA, Patil S, Davenport S, Goldstein D, Piskens J (1986) Duchenne muscular dystrophy, glycerol kinase deficiency, and adrenal insufficiency associated with Xp21 interstitial deletion. J Pediatr 108:189?192
5. Bertelson CJ, Bartley JA, Monaco AM, Colletti-Feener C, Fischbeck K, Kunkel LM (1986) Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. J Med Genet 23:531?537
Cited by
27 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献