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MRX8: an X-linked mental retardation condition with linkage to Xq21.
Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE. Schwartz CE, et al. Among authors: ledbetter d. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):467-74. doi: 10.1002/ajmg.1320430170. Am J Med Genet. 1992. PMID: 1605227
Report of the committee on cytogenetic markers.
Sutherland GR, Ledbetter DH. Sutherland GR, et al. Among authors: ledbetter dh. Cytogenet Cell Genet. 1989;51(1-4):452-8. doi: 10.1159/000132804. Cytogenet Cell Genet. 1989. PMID: 2676381 Review. No abstract available.
Second international workshop on human chromosome 17.
Fain PR, Solomon E, Ledbetter DH. Fain PR, et al. Among authors: ledbetter dh. Cytogenet Cell Genet. 1991;57(2-3):66-77. Cytogenet Cell Genet. 1991. PMID: 1914524 Review. No abstract available.
Intellectual disability is associated with increased runs of homozygosity in simplex autism.
Gamsiz ED, Viscidi EW, Frederick AM, Nagpal S, Sanders SJ, Murtha MT, Schmidt M; Simons Simplex Collection Genetics Consortium; Triche EW, Geschwind DH, State MW, Istrail S, Cook EH Jr, Devlin B, Morrow EM. Gamsiz ED, et al. Am J Hum Genet. 2013 Jul 11;93(1):103-9. doi: 10.1016/j.ajhg.2013.06.004. Epub 2013 Jul 3. Am J Hum Genet. 2013. PMID: 23830515 Free PMC article.
465 results