Brown WT - Search Results

1

Pergolizzi RG, Erster SH, Goonewardena P, Brown WT. Pergolizzi RG, et al. Among authors: brown wt. Lancet. 1992 Feb 1;339(8788):271-2. doi: 10.1016/0140-6736(92)91334-5. Lancet. 1992. PMID: 1346284 Free article.

2

Polymerase chain reaction analysis of fragile X mutations.

Erster SH, Brown WT, Goonewardena P, Dobkin CS, Jenkins EC, Pergolizzi RG. Erster SH, et al. Among authors: brown wt. Hum Genet. 1992 Sep-Oct;90(1-2):55-61. doi: 10.1007/BF00210744. Hum Genet. 1992. PMID: 1427787

3

Prenatally detected fragile X females: long-term follow-up studies show high risk of mental impairment.

Brown WT, Jenkins EC, Goonewardena P, Miezejeski C, Atkin J, Devys D. Brown WT, et al. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):96-102. doi: 10.1002/ajmg.1320430114. Am J Med Genet. 1992. PMID: 1605241

4

Detection of fragile X non-penetrant males by DNA marker analysis.

Brown WT, Gross A, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC. Brown WT, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):292-7. doi: 10.1002/ajmg.1320380226. Am J Med Genet. 1991. PMID: 1673300

5

Linkage in fragile X families of three distal flanking markers: ST14, DX13, and F8.

Brown WT, Gross AC, Goonewardena P, Ferrando C, Dobkin C, Jenkins EC. Brown WT, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):343-6. doi: 10.1002/ajmg.1320380235. Am J Med Genet. 1991. PMID: 1673308

6

Molecular characterization of a DNA probe, U6.2, located close to the fragile X locus.

Pergolizzi R, Brown WT, Goonewardena P, Bhan R, Dobkin C, Dahl N, Pettersson U. Pergolizzi R, et al. Among authors: brown wt. Am J Med Genet. 1991 Feb-Mar;38(2-3):380-3. doi: 10.1002/ajmg.1320380245. Am J Med Genet. 1991. PMID: 1673315

7

Molecular markers of fragile X: application to males at risk in fragile X families.

Brown WT, Goonewardena P, Gross AC, Dobkin C, Jenkins EC. Brown WT, et al. Prog Clin Biol Res. 1991;368:73-7. Prog Clin Biol Res. 1991. PMID: 1946507 No abstract available.

8

Evidence of founder chromosomes in fragile X syndrome.

Richards RI, Holman K, Friend K, Kremer E, Hillen D, Staples A, Brown WT, Goonewardena P, Tarleton J, Schwartz C, et al. Richards RI, et al. Among authors: brown wt. Nat Genet. 1992 Jul;1(4):257-60. doi: 10.1038/ng0792-257. Nat Genet. 1992. PMID: 1302021

9

Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304.

Goonewardena P, Brown WT, Gross AC, Ferrando C, Dobkin C, Romano V, Bosco P, Ceratto N, Pettersson U, Dahl N. Goonewardena P, et al. Among authors: brown wt. Am J Med Genet. 1991 Feb-Mar;38(2-3):322-7. doi: 10.1002/ajmg.1320380231. Am J Med Genet. 1991. PMID: 1673305

10

Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.

McConkie-Rosell A, Lachiewicz AM, Spiridigliozzi GA, Tarleton J, Schoenwald S, Phelan MC, Goonewardena P, Ding X, Brown WT. McConkie-Rosell A, et al. Among authors: brown wt. Am J Hum Genet. 1993 Oct;53(4):800-9. Am J Hum Genet. 1993. PMID: 8213810 Free PMC article.

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