Dobkin C - Search Results

1

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: dobkin c. Am J Med Genet. 1991 Feb-Mar;38(2-3):322-7. doi: 10.1002/ajmg.1320380231. Am J Med Genet. 1991. PMID: 1673305

2

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. Among authors: dobkin c. Am J Med Genet. 1991 Feb-Mar;38(2-3):292-7. doi: 10.1002/ajmg.1320380226. Am J Med Genet. 1991. PMID: 1673300

3

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. Among authors: dobkin c. Am J Med Genet. 1991 Feb-Mar;38(2-3):343-6. doi: 10.1002/ajmg.1320380235. Am J Med Genet. 1991. PMID: 1673308

4

Cytogenetically negative, linkage positive "fragile X" syndrome.

Sklower Brooks S, Cohen I, Ferrando C, Jenkins EC, Brown WT, Dobkin C. Sklower Brooks S, et al. Among authors: dobkin c. Am J Med Genet. 1991 Feb-Mar;38(2-3):370-3. doi: 10.1002/ajmg.1320380242. Am J Med Genet. 1991. PMID: 1673313

5

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: dobkin c. Am J Med Genet. 1991 Feb-Mar;38(2-3):380-3. doi: 10.1002/ajmg.1320380245. Am J Med Genet. 1991. PMID: 1673315

6

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. Among authors: dobkin c. Prog Clin Biol Res. 1991;368:73-7. Prog Clin Biol Res. 1991. PMID: 1946507 No abstract available.

7

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: dobkin cs. Hum Genet. 1992 Sep-Oct;90(1-2):55-61. doi: 10.1007/BF00210744. Hum Genet. 1992. PMID: 1427787

8

Polymerase chain reaction detection of the Dde I polymorphism in the factor 9 gene for fragile X linkage analysis.

Dobkin CS, Driscoll MC, Ferrando C. Dobkin CS, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):378-9. doi: 10.1002/ajmg.1320380244. Am J Med Genet. 1991. PMID: 2018077

9

Multipoint linkage of 9 anonymous probes to HPRT, factor 9, and fragile X.

Brown WT, Ye W, Gross AC, Chan CB, Dobkin CS, Jenkins EC. Brown WT, et al. Among authors: dobkin cs. Am J Med Genet. 1988 May-Jun;30(1-2):551-66. doi: 10.1002/ajmg.1320300157. Am J Med Genet. 1988. PMID: 2902796

10

Pulsed-field gradient-gel studies around the fragile site.

Dobkin CS, Brown WT. Dobkin CS, et al. Am J Med Genet. 1988 May-Jun;30(1-2):593-600. doi: 10.1002/ajmg.1320300160. Am J Med Genet. 1988. PMID: 2902798

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