Single-tube multiplex-PCR screen for common deletional determinants of α-thalassemia von CHONG, S. S, BOEHM, C. D, HIGGS, D. R, CUTTING, G. R

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Switch from Monoallelic to Biallelic Human IGF2 Promoter Methylation during Aging and Carcinogenesis von Issa, Jean-Pierre J., Vertino, Paula M., Boehm, Corinne D., Newsham, Irene F., Baylin, Stephen B.

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Simplified multiplex-PCR diagnosis of common southeast Asian deletional determinants of α-thalassemia von CHONG, Samuel S, BOEHM, Corinne D, CUTTING, Garry R, HIGGS, Douglas R

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ABCD1 mutations and the X-linked adrenoleukodystrophy mutation database: Role in diagnosis and clinical correlations von Kemp, Stephan, Pujol, Aurora, Waterham, Hans R., van Geel, Björn M., Boehm, Corinne D., Raymond, Gerald V., Cutting, Garry R., Wanders, Ronald J.A., Moser, Hugo W.

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Cystic fibrosis carrier population screening in the primary care setting von LOADER, S, CALDWELL, P, KOZYRA, A, LEVENKRON, J. C, BOEHM, C. D, KAZAZIAN, H. H, ROWLEY, P. T

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Molecular Basis and Prenatal Diagnosis of β-Thalassemia von Kazazian, Haig H., Boehm, Corinne D.

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Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes von Saiki, Randall K, Chang, Chu-An, Levenson, Corey H, Warren, Tina C, Boehm, Corinne D, Kazazian, Haig H, Erlich, Henry A

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Robust fragile X (CGG)n genotype classification using a methylation specific triple PCR assay von Zhou, Y, Law, H-Y, Boehm, C D, Yoon, C-S, Cutting, G R, Ng, I S L, Chong, S S

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The development of a highly informative mouse Simple Sequence Length Polymorphism (SSLP) marker set and construction of a mouse family tree using parsimony analysis von Witmer, Philip D, Doheny, Kimberly F, Adams, Marcia K, Boehm, Corinne D, Dizon, Jane S, Goldstein, Janet L, Templeton, Tira M, Wheaton, Ariana M, Dong, Penny N, Pugh, Elizabeth W, Nussbaum, Robert L, Hunter, Kent, Kelmenson, Jennifer A, Rowe, Lucy B, Brownstein, Michael J

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Frequency and stability of the fragile X premutation von Reiss, Allan L., Kazazian, Haig H., Krebs, Claudia M., McAughan, Audrey, Boehm, Corinne D., Abrams, Michael T., Nelson, David L.

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Nonuniform recombination within the human beta-globin gene cluster von Chakravarti, A, Buetow, K H, Antonarakis, S E, Waber, P G, Boehm, C D, Kazazian, H H

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Nonrandom Association of Polymorphic Restriction Sites in the β -globin Gene Cluster von Antonarakis, Stylianos E., Boehm, Corinne D., Patricia J. V. Giardina, Kazazian, Haig H.

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Accurate DNA-Based Diagnostic and Carrier Testing for X-Linked Adrenoleukodystrophy von Boehm, Corinne D., Cutting, Garry R., Lachtermacher, Marcia B., Moser, Hugo W., Chong, Samuel S.

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ACMG recommendations for standards for interpretation of sequence variations von Kazazian, Haig H., Boehm, Corinne D., Seltzer, William K.

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Origin of the βS-globin Gene in Blacks: The Contribution of Recurrent Mutation or Gene Conversion or Both von Antonarakis, Stylianos E., Boehm, Corinne D., Serjeant, Graham R., Theisen, Catherine E., Dover, George J., Kazazian, Haig H.

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Familial neurofibromatosis type 1: Clinical experience with DNA testing von Hofman, Karen J., Boehm, Corinne D.

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Molecular basis and prenatal diagnosis of beta-thalassemia von Kazazian, HH Jr, Boehm, CD

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Characterization of a spontaneous mutation to a β-thalassemia allele von KAZAZIAN, H. H. JR, ORKIN, S. H, BOEHM, C. D, GOFF, S. C, WONG, C, DOWLING, C. E, NEWBURGER, P. E, KNOWLTON, R. G, BROWN, V, DONIS-KELLER, H

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A new retrotransposable human L1 element from the LRE2 locus on chromosome 1q produces a chimaeric insertion von Holmes, Susan E, Dombroski, Beth A, Krebs, Claudia M, Boehm, Corinne D, Kazazian, Haig H

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Evidence for Multiple Origins of the βE-globin Gene in Southeast Asia von Antonarakis, Stylianos E., Orkin, Stuart H., Kazazian, Haig H., Goff, Sabra C., Boehm, Corinne D., Waber, Pamela G., Sexton, Julianne P., Ostrer, Harry, Fairbanks, Virgil F., Chakravarti, Aravinda

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