Phelan MC - Search Results

1

The parental origin and mechanism of formation of three dicentric X chromosomes.

Phelan MC, Prouty LA, Stevenson RE, Howard-Peebles PN, Page DC, Schwartz CE. Phelan MC, et al. Hum Genet. 1988 Sep;80(1):81-4. doi: 10.1007/BF00451462. Hum Genet. 1988. PMID: 3417308

2

Deletion mapping of plasminogen activator inhibitor, type I (PLANH1) and beta-glucuronidase (GUSB) in 7q21----q22.

Schwartz CE, Stanislovitis P, Phelan MC, Klinger K, Taylor HA, Stevenson RE. Schwartz CE, et al. Among authors: phelan mc. Cytogenet Cell Genet. 1991;56(3-4):152-3. doi: 10.1159/000133073. Cytogenet Cell Genet. 1991. PMID: 2055109

3

Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21.

Phelan MC, Morton CC, Stevenson RE, Tanzi RE, Stewart GD, Watkins PC, Gusella JF, Amos JA. Phelan MC, et al. Am J Hum Genet. 1988 Oct;43(4):511-9. Am J Hum Genet. 1988. PMID: 2902789 Free PMC article.

4

Detection of submicroscopic deletions in band 17p13 in patients with the Miller-Dieker syndrome.

Schwartz CE, Johnson JP, Holycross B, Mandeville TM, Sears TS, Graul EA, Carey JC, Schroer RJ, Phelan MC, Szollar J, et al. Schwartz CE, et al. Among authors: phelan mc. Am J Hum Genet. 1988 Nov;43(5):597-604. Am J Hum Genet. 1988. PMID: 2903661 Free PMC article.

5

Recombinant chromosome 9 possibly derived from breakage and reunion of sister chromatids within a paracentric inversion loop.

Phelan MC, Stevenson RE, Anderson EV Jr. Phelan MC, et al. Am J Med Genet. 1993 May 15;46(3):304-8. doi: 10.1002/ajmg.1320460313. Am J Med Genet. 1993. PMID: 8488876

6

Physical mapping of probes proximal to the fragile X locus (FRAX) confirms the order F9-DXS105 (cX55.7)-DXS98 (4D8)-FRAXA.

Sauer SM, Phelan MC, Richer CL, Schwartz CE. Sauer SM, et al. Among authors: phelan mc. Cytogenet Cell Genet. 1989;50(2-3):172-3. doi: 10.1159/000132753. Cytogenet Cell Genet. 1989. PMID: 2776486

7

Fragile X syndrome and neoplasia.

Phelan MC, Stevenson RE, Collins JL, Trent HE 3rd. Phelan MC, et al. Am J Med Genet. 1988 May-Jun;30(1-2):77-82. doi: 10.1002/ajmg.1320300106. Am J Med Genet. 1988. PMID: 2845782

8

Fragile X syndrome: linkage analysis in black and white populations.

Schwartz CE, Phelan MC, Brightharp C, Pancoast I, Howard-Peebles PN, Thibodeau S, Brown WT, Jenkins EC. Schwartz CE, et al. Among authors: phelan mc. Am J Med Genet. 1988 May-Jun;30(1-2):531-42. doi: 10.1002/ajmg.1320300155. Am J Med Genet. 1988. PMID: 3177470

9

Fragile X syndrome: incidence, clinical and cytogenetic findings in the black and white populations of South Carolina.

Schwartz CE, Phelan MC, Pulliam LH, Wilkes G, Vanner LV, Albiez KL, Potts WA, Rogers RC, Schroer RJ, Saul RA, et al. Schwartz CE, et al. Among authors: phelan mc. Am J Med Genet. 1988 May-Jun;30(1-2):641-54. doi: 10.1002/ajmg.1320300165. Am J Med Genet. 1988. PMID: 3177476

10

Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Schwartz C, Fitch N, Phelan MC, Richer CL, Stevenson R. Schwartz C, et al. Among authors: phelan mc. Hum Genet. 1987 May;76(1):54-7. doi: 10.1007/BF00283050. Hum Genet. 1987. PMID: 3471705

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