Ledbetter D - Search Results

1

Fine mapping of the cystinosis gene using an integrated genetic and physical map of a region within human chromosome band 17p13.

McDowell G, Isogai T, Tanigami A, Hazelwood S, Ledbetter D, Polymeropoulos MH, Lichter-Konecki U, Konecki D, Town MM, Van't Hoff WV, Weissenbach J, Gahl WA. McDowell G, et al. Among authors: ledbetter d. Biochem Mol Med. 1996 Aug;58(2):135-41. doi: 10.1006/bmme.1996.0041. Biochem Mol Med. 1996. PMID: 8812732

2

Localization of the cellular retinoic acid binding protein (CRABP) gene relative to the acute promyelocytic leukemia-associated breakpoint on human chromosome 15.

Geurts van Kessel A, de Leeuw H, Dekker EJ, Rijks L, Spurr N, Ledbetter D, Kootwijk E, Vaessen MJ. Geurts van Kessel A, et al. Among authors: ledbetter d. Hum Genet. 1991 Jun;87(2):201-4. doi: 10.1007/BF00204182. Hum Genet. 1991. PMID: 1648546 Free article.

3

Molecular definition of the Prader-Willi syndrome chromosome region and orientation of the SNRPN gene.

Buiting K, Dittrich B, Gross S, Greger V, Lalande M, Robinson W, Mutirangura A, Ledbetter D, Horsthemke B. Buiting K, et al. Among authors: ledbetter d. Hum Mol Genet. 1993 Dec;2(12):1991-4. doi: 10.1093/hmg/2.12.1991. Hum Mol Genet. 1993. PMID: 8111365

4

Report of the committee on the genetic constitution of chromosome 17.

Solomon E, Ledbetter DH. Solomon E, et al. Among authors: ledbetter dh. Cytogenet Cell Genet. 1990;55(1-4):198-215. doi: 10.1159/000133013. Cytogenet Cell Genet. 1990. PMID: 2073835 Review. No abstract available.

5

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.

6

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

7

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

8

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

9

Comparative genomic hybridization: a comparison with molecular and cytogenetic analysis.

Nacheva EP, Grace CD, Bittner M, Ledbetter DH, Jenkins RB, Green AR. Nacheva EP, et al. Among authors: ledbetter dh. Cancer Genet Cytogenet. 1998 Jan 15;100(2):93-105. doi: 10.1016/s0165-4608(97)00021-6. Cancer Genet Cytogenet. 1998. PMID: 9428351

10

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.

Hanson E, Bernier R, Porche K, Jackson FI, Goin-Kochel RP, Snyder LG, Snow AV, Wallace AS, Campe KL, Zhang Y, Chen Q, D'Angelo D, Moreno-De-Luca A, Orr PT, Boomer KB, Evans DW, Kanne S, Berry L, Miller FK, Olson J, Sherr E, Martin CL, Ledbetter DH, Spiro JE, Chung WK; Simons Variation in Individuals Project Consortium. Hanson E, et al. Among authors: ledbetter dh, d angelo d. Biol Psychiatry. 2015 May 1;77(9):785-93. doi: 10.1016/j.biopsych.2014.04.021. Epub 2014 Jun 16. Biol Psychiatry. 2015. PMID: 25064419 Free PMC article.

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