Howard-Peebles PN - Search Results

1

The fragile X premutation in carriers and its effect on mutation size in offspring.

Fisch GS, Snow K, Thibodeau SN, Chalifaux M, Holden JJ, Nelson DL, Howard-Peebles PN, Maddalena A. Fisch GS, et al. Am J Hum Genet. 1995 May;56(5):1147-55. Am J Hum Genet. 1995. PMID: 7726171 Free PMC article.

2

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

3

Is fragile X syndrome a pervasive developmental disability? Cognitive ability and adaptive behavior in males with the full mutation.

Fisch GS, Holden JJ, Simensen R, Carpenter N, Howard-Peebles PN, Maddalena A, Sandgrund A, Jacques JR, McGann B. Fisch GS, et al. Am J Med Genet. 1994 Jul 15;51(4):346-52. doi: 10.1002/ajmg.1320510410. Am J Med Genet. 1994. PMID: 7942997

4

Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: a prospective multicenter analysis.

Fisch GS, Simensen R, Tarleton J, Chalifoux M, Holden JJ, Carpenter N, Howard-Peebles PN, Maddalena A. Fisch GS, et al. Am J Med Genet. 1996 Aug 9;64(2):356-61. doi: 10.1002/(SICI)1096-8628(19960809)64:2<356::AID-AJMG24>3.0.CO;2-D. Am J Med Genet. 1996. PMID: 8844080

5

Lack of association between mutation size and cognitive/behavior deficits in fragile X males: a brief report.

Fisch GS, Carpenter N, Howard-Peebles PN, Maddalena A, Simensen R, Tarleton J, Julien-Inalsingh C, Chalifoux M, Holden JJ. Fisch GS, et al. Am J Med Genet. 1996 Aug 9;64(2):362-4. doi: 10.1002/(SICI)1096-8628(19960809)64:2<362::AID-AJMG25>3.0.CO;2-C. Am J Med Genet. 1996. PMID: 8844081

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

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

8

Prenatal diagnosis in known fragile X carriers.

Maddalena A, Hicks BD, Spence WC, Levinson G, Howard-Peebles PN. Maddalena A, et al. Am J Med Genet. 1994 Jul 15;51(4):490-6. doi: 10.1002/ajmg.1320510439. Am J Med Genet. 1994. PMID: 7943026

9

Improved sizing of fragile X CCG repeats by nested polymerase chain reaction.

Levinson G, Maddalena A, Palmer FT, Harton GL, Bick DP, Howard-Peebles PN, Black SH, Schulman JD. Levinson G, et al. Am J Med Genet. 1994 Jul 15;51(4):527-34. doi: 10.1002/ajmg.1320510448. Am J Med Genet. 1994. PMID: 7943035

10

A fragile X mosaic male with a cryptic full mutation detected in epithelium but not in blood.

Maddalena A, Yadvish KN, Spence WC, Howard-Peebles PN. Maddalena A, et al. Am J Med Genet. 1996 Aug 9;64(2):309-12. doi: 10.1002/(SICI)1096-8628(19960809)64:2<309::AID-AJMG15>3.0.CO;2-J. Am J Med Genet. 1996. PMID: 8844071

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