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Van den Ouweland, AMW, Deelen, WH, Kunst, CB, Uzielli, M-L G, Nelson, DL, Warren, ST, Oostra, BA and Halley, DJJ: Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes. Human Molecular Genetics 3:1823-1827 (1994). |
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Malter, HE, Tucker, MJ and Warren, ST: Fragile X syndrome and trinucleotide repeat expansion mutations: New challenges for genetic analysis and diagnosis. Assisted Reproduction Review 4:67-73 (1994). |
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Kunst CB and Warren, ST: Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles. Cell 77:853-861 (1994). |
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Riggins, GJ, Zhang, F and Warren, ST: Lack of imprinting of BCR. Nature Genetics 6:226 (1994). |
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Warren, ST and Nelson, DL: Advances in molecular analysis of fragile X syndrome. Journal of the American Medical Association 271:536-542 (1994).
• Japanese translation of the above article in: Advances in Research on Autism and Developmental Disorders, (R. Takagi, M. Rutter, E. Schopler, Eds.) Volume 2, pp. 124-135 (1998). |
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Riggins, GJ, Sherman, SL, Philips, CN, Stock, W, Westbrook, CA and Warren, ST: CGG-repeat polymorphism of the BCR gene rules out predisposing alleles leading to the Philadelphia chromosome. Genes, Chromosomes, and Cancer 9:141-144 (1994). |
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