Ledbetter D - Search Results

1

Spastic paraplegia with iron deposits in the basal ganglia: a new X-linked mental retardation syndrome.

Arena JF, Schwartz C, Stevenson R, Lawrence L, Carpenter A, Duara R, Ledbetter D, Huang T, Lehner T, Ott J, et al. Arena JF, et al. Among authors: ledbetter d. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):479-90. doi: 10.1002/ajmg.1320430172. Am J Med Genet. 1992. PMID: 1605230

2

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

3

Mapping of a cerebellar degeneration related protein and DXS304 around the fragile site.

Hirst MC, Bell MV, MacKinnon RN, Watson JE, Callen D, Sutherland G, Dahl N, Patterson MN, Schwartz C, Ledbetter D, et al. Hirst MC, et al. Among authors: ledbetter d. Am J Med Genet. 1991 Feb-Mar;38(2-3):354-6. doi: 10.1002/ajmg.1320380238. Am J Med Genet. 1991. PMID: 1673311

4

Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes".

Estabrooks LL, Breg WR, Hayden MR, Ledbetter DH, Myers RM, Wyandt HE, Yang-Feng TL, Hirschhorn K. Estabrooks LL, et al. Among authors: ledbetter dh. Am J Med Genet. 1995 Feb 13;55(4):453-8. doi: 10.1002/ajmg.1320550412. Am J Med Genet. 1995. PMID: 7762585 Review.

5

Clinical phenotype of the recurrent 1q21.1 copy-number variant.

Bernier R, Steinman KJ, Reilly B, Wallace AS, Sherr EH, Pojman N, Mefford HC, Gerdts J, Earl R, Hanson E, Goin-Kochel RP, Berry L, Kanne S, Snyder LG, Spence S, Ramocki MB, Evans DW, Spiro JE, Martin CL, Ledbetter DH, Chung WK; Simons VIP consortium. Bernier R, et al. Genet Med. 2016 Apr;18(4):341-9. doi: 10.1038/gim.2015.78. Epub 2015 Jun 11. Genet Med. 2016. PMID: 26066539 Free PMC article.

6

Familial Prader-Willi syndrome with apparently normal chromosomes.

Lubinsky M, Zellweger H, Greenswag L, Larson G, Hansmann I, Ledbetter D. Lubinsky M, et al. Among authors: ledbetter d. Am J Med Genet. 1987 Sep;28(1):37-43. doi: 10.1002/ajmg.1320280106. Am J Med Genet. 1987. PMID: 3674116

7

"New microdeletion syndromes: complex, but no new paradigms".

Ledbetter DH. Ledbetter DH. J Med Genet. 2009 Aug;46(8):576. doi: 10.1136/jmg.2009.068916. J Med Genet. 2009. PMID: 19648125 No abstract available.

8

14-3-3epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome.

Toyo-oka K, Shionoya A, Gambello MJ, Cardoso C, Leventer R, Ward HL, Ayala R, Tsai LH, Dobyns W, Ledbetter D, Hirotsune S, Wynshaw-Boris A. Toyo-oka K, et al. Among authors: ledbetter d. Nat Genet. 2003 Jul;34(3):274-85. doi: 10.1038/ng1169. Nat Genet. 2003. PMID: 12796778

9

Journal policies concerning free access to scientific materials.

Ledbetter DH. Ledbetter DH. Am J Med Genet. 1991 Jun 1;39(3):371-2. doi: 10.1002/ajmg.1320390324. Am J Med Genet. 1991. PMID: 1867293 No abstract available.

10

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.

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