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Prenatal diagnosis in known fragile X carriers.
Maddalena A, Hicks BD, Spence WC, Levinson G, Howard-Peebles PN. Maddalena A, et al. Among authors: spence wc. Am J Med Genet. 1994 Jul 15;51(4):490-6. doi: 10.1002/ajmg.1320510439. Am J Med Genet. 1994. PMID: 7943026
Molecular fragile X screening in normal populations.
Spence WC, Black SH, Fallon L, Maddalena A, Cummings E, Menapace-Drew G, Bick DP, Levinson G, Schulman JD, Howard-Peebles PN. Spence WC, et al. Am J Med Genet. 1996 Jul 12;64(1):181-3. doi: 10.1002/(SICI)1096-8628(19960712)64:1<181::AID-AJMG31>3.0.CO;2-H. Am J Med Genet. 1996. PMID: 8826471
Fragile X screening: what is the real issue?
Howard-Peebles PN, Maddalena A, Spence WC, Levinson G, Fallon L, Bick DP, Black SH, Schulman JD. Howard-Peebles PN, et al. Among authors: spence wc. Am J Med Genet. 1994 Dec 1;53(4):382. doi: 10.1002/ajmg.1320530417. Am J Med Genet. 1994. PMID: 7864051 No abstract available.
DNA-based prenatal determination of the RhEe genotype.
Spence WC, Potter P, Maddalena A, Demers DB, Bick DP. Spence WC, et al. Obstet Gynecol. 1995 Oct;86(4 Pt 2):670-2. doi: 10.1016/0029-7844(95)00093-7. Obstet Gynecol. 1995. PMID: 7675408
16 results