Howard-Peebles PN - 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

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. Am J Med Genet. 1988 May-Jun;30(1-2):531-42. doi: 10.1002/ajmg.1320300155. Am J Med Genet. 1988. PMID: 3177470

3

Obstetrical and gynecological complications in fragile X carriers: a multicenter study.

Schwartz CE, Dean J, Howard-Peebles PN, Bugge M, Mikkelsen M, Tommerup N, Hull C, Hagerman R, Holden JJ, Stevenson RE. Schwartz CE, et al. Am J Med Genet. 1994 Jul 15;51(4):400-2. doi: 10.1002/ajmg.1320510419. Am J Med Genet. 1994. PMID: 7943006

4

Survey of the fragile X syndrome CGG repeat and the short-tandem-repeat and single-nucleotide-polymorphism haplotypes in an African American population.

Crawford DC, Schwartz CE, Meadows KL, Newman JL, Taft LF, Gunter C, Brown WT, Carpenter NJ, Howard-Peebles PN, Monaghan KG, Nolin SL, Reiss AL, Feldman GL, Rohlfs EM, Warren ST, Sherman SL. Crawford DC, et al. Among authors: howard peebles pn. Am J Hum Genet. 2000 Feb;66(2):480-93. doi: 10.1086/302762. Am J Hum Genet. 2000. PMID: 10677308 Free PMC article.

5

Longitudinal changes in IQ among fragile X males: clinical evidence of more than one mutation?

Fisch GS, Shapiro LR, Simensen R, Schwartz CE, Fryns JP, Borghgraef M, Curfs LM, Howard-Peebles PN, Arinami T, Mavrou A. Fisch GS, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):28-34. doi: 10.1002/ajmg.1320430105. Am J Med Genet. 1992. PMID: 1605202

6

Relationship between age and IQ among fragile X males: a multicenter study.

Fisch GS, Arinami T, Froster-Iskenius U, Fryns JP, Curfs LM, Borghgraef M, Howard-Peebles PN, Schwartz CE, Simensen RJ, Shapiro LR. Fisch GS, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):481-7. doi: 10.1002/ajmg.1320380268. Am J Med Genet. 1991. PMID: 2018090

7

Characteristics of the transmission of the FMR1 gene from carrier females in a prospective sample of conceptuses.

Sherman SL, Maddalena A, Howard-Peebles PN, Brown WT, Nolin S, Jenkins E, Schwartz C, Tarrelton J, Shapiro LR, Smits AP, et al. Sherman SL, et al. Am J Med Genet. 1994 Jul 15;51(4):503-6. doi: 10.1002/ajmg.1320510442. Am J Med Genet. 1994. PMID: 7943029

8

Characterization of seven DA/DAPI-positive bisatellited marker chromosomes by in situ hybridization.

Plattner R, Heerema NA, Patil SR, Howard-Peebles PN, Palmer CG. Plattner R, et al. Hum Genet. 1991 Jul;87(3):290-6. doi: 10.1007/BF00200906. Hum Genet. 1991. PMID: 1864603

9

Clinical findings in patients with marker chromosomes identified by fluorescence in situ hybridization.

Plattner R, Heerema NA, Howard-Peebles PN, Miles JH, Soukup S, Palmer CG. Plattner R, et al. Hum Genet. 1993 Jul;91(6):589-98. doi: 10.1007/BF00205086. Hum Genet. 1993. PMID: 8340114

10

Familial X-linked mental retardation, verbal disability, and marker X chromosomes.

Howard-Peebles PN, Stoddard GR, Mims MG. Howard-Peebles PN, et al. Am J Hum Genet. 1979 Mar;31(2):214-22. Am J Hum Genet. 1979. PMID: 453204 Free PMC article.

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