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X-chromosomal gene in Leber hereditary optic neuroretinopathy.
Chen JD, Denton MJ. Chen JD, et al. Am J Hum Genet. 1991 Sep;49(3):692-3. Am J Hum Genet. 1991. PMID: 1882847 Free PMC article. No abstract available.
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM. Koenig M, et al. Am J Hum Genet. 1989 Oct;45(4):498-506. Am J Hum Genet. 1989. PMID: 2491009 Free PMC article.
X-linked megalocornea: close linkage to DXS87 and DXS94.
Chen JD, Mackey D, Fuller H, Serravalle S, Olsson J, Denton MJ. Chen JD, et al. Hum Genet. 1989 Oct;83(3):292-4. doi: 10.1007/BF00285176. Hum Genet. 1989. PMID: 2571565
Linkage heterogeneity between X-linked retinitis pigmentosa and a map of 10 RFLP loci.
Chen JD, Halliday F, Keith G, Sheffield L, Dickinson P, Gray R, Constable I, Denton M. Chen JD, et al. Am J Hum Genet. 1989 Sep;45(3):401-11. Am J Hum Genet. 1989. PMID: 2570529 Free PMC article.
Non-allelic mutations in X-linked retinitis pigmentosa.
Chen JD, Dickinson P, Gray R, Constable I, Sheffield L, Denton MJ. Chen JD, et al. Clin Genet. 1989 May;35(5):338-42. doi: 10.1111/j.1399-0004.1989.tb02954.x. Clin Genet. 1989. PMID: 2569369
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