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DNA-based genetic testing in fifty fragile X families.
Murphy PD, Watson MS, Shapiro LR, Wilmot PL, Breg WR. Murphy PD, et al. Among authors: breg wr. Am J Med Genet. 1991 Feb-Mar;38(2-3):305-10. doi: 10.1002/ajmg.1320380228. Am J Med Genet. 1991. PMID: 1673302
Aneuploidy and the fragile X syndrome.
Watson MS, Breg WR, Pauls D, Brown WT, Carroll AJ, Howard-Peebles PN, Meryash D, Shapiro LR. Watson MS, et al. Among authors: breg wr. Am J Med Genet. 1988 May-Jun;30(1-2):115-21. doi: 10.1002/ajmg.1320300110. Am J Med Genet. 1988. PMID: 2972203
Chromosome deletion 1q42-43.
Watson MS, Gargus JJ, Blakemore KJ, Katz SN, Breg WR. Watson MS, et al. Among authors: breg wr. Am J Med Genet. 1986 May;24(1):1-6. doi: 10.1002/ajmg.1320240102. Am J Med Genet. 1986. PMID: 3706398
Fragile X in a survey of 75 autistic males.
Watson MS, Leckman JF, Annex B, Breg WR, Boles D, Volkmar FR, Cohen DJ, Carter C. Watson MS, et al. Among authors: breg wr. N Engl J Med. 1984 May 31;310(22):1462. doi: 10.1056/NEJM198405313102214. N Engl J Med. 1984. PMID: 6717529 No abstract available.
Deletion (12)(q15q21.2).
Watson MS, McAllister-Barton L, Mahoney MJ, Breg WR. Watson MS, et al. Among authors: breg wr. J Med Genet. 1989 May;26(5):343-4. doi: 10.1136/jmg.26.5.343. J Med Genet. 1989. PMID: 2543819 Free PMC article. No abstract available.
101 results