Barker DF - Search Results

1

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: barker df. 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

2

A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.

Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D, et al. Tranebjaerg L, et al. J Med Genet. 1995 Apr;32(4):257-63. doi: 10.1136/jmg.32.4.257. J Med Genet. 1995. PMID: 7643352 Free PMC article.

3

Charcot-Marie-Tooth neuropathy type 1A mutation: apparent crossovers with D17S122 are due to a duplication.

Nicholson GA, Kennerson ML, Keats BJ, Mesterovic N, Churcher W, Barker D, Ross DA. Nicholson GA, et al. Am J Med Genet. 1992 Nov 1;44(4):455-60. doi: 10.1002/ajmg.1320440414. Am J Med Genet. 1992. PMID: 1442887

4

Identification of more than 500 RFLPs by screening random genomic clones.

Schumm JW, Knowlton RG, Braman JC, Barker DF, Botstein D, Akots G, Brown VA, Gravius TC, Helms C, Hsiao K, et al. Schumm JW, et al. Among authors: barker df. Am J Hum Genet. 1988 Jan;42(1):143-59. Am J Hum Genet. 1988. PMID: 2892396 Free PMC article.

5

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

Solomon E, Barker DF. Solomon E, et al. Among authors: barker df. Cytogenet Cell Genet. 1989;51(1-4):319-37. doi: 10.1159/000132797. Cytogenet Cell Genet. 1989. PMID: 2676375 Review. No abstract available.

6

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

Solomon E, Barker D. Solomon E, et al. Cytogenet Cell Genet. 1988;49(1-3):95-8. doi: 10.1159/000132658. Cytogenet Cell Genet. 1988. PMID: 3203559 No abstract available.

7

Parental origin-dependent, male offspring-specific transmission-ratio distortion at loci on the human X chromosome.

Naumova AK, Leppert M, Barker DF, Morgan K, Sapienza C. Naumova AK, et al. Among authors: barker df. Am J Hum Genet. 1998 Jun;62(6):1493-9. doi: 10.1086/301860. Am J Hum Genet. 1998. PMID: 9585588 Free PMC article.

8

Linkage of Charcot-Marie-Tooth neuropathy type 1a to chromosome 17.

Vance JM, Nicholson GA, Yamaoka LH, Stajich J, Stewart CS, Speer MC, Hung WY, Roses AD, Barker D, Pericak-Vance MA. Vance JM, et al. Exp Neurol. 1989 May;104(2):186-9. doi: 10.1016/s0014-4886(89)80013-5. Exp Neurol. 1989. PMID: 2707366

9

Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2.

Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, Fischbeck K, Roses AD, Pericak-Vance MA. Vance JM, et al. Genomics. 1991 Apr;9(4):623-8. doi: 10.1016/0888-7543(91)90355-i. Genomics. 1991. PMID: 1674726

10

Properties of the translocatable tetracycline-resistance element Tn10 in Escherichia coli and bacteriophage lambda.

Kleckner N, Barker DF, Ross DG, Botstein D. Kleckner N, et al. Among authors: barker df. Genetics. 1978 Nov;90(3):427-61. doi: 10.1093/genetics/90.3.427. Genetics. 1978. PMID: 365678 Free PMC article.

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