Primary structure of dystrophin-related protein von Tinsley, J. M., Blake, D. J., Roche, A., Fairbrother, U., Riss, J., Byth, B. C., Knight, A. E., Kendrick-Jones, J., Suthers, G. K., Love, D. R., Edwards, Y. H., Davies, K. E.

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Genetic homogeneity between acute and chronic forms of spinal muscular atrophy von Gilliam, T. C., Brzustowicz, L. M., Castilla, L. H., Lehner, T., Penchaszadeh, G. K., Daniels, R. J., Byth, B. C., Knowles, J., Hislop, J. E., Shapira, Y., Dubowitz, V., Munsat, T. L., Ott, J., Davies, K. E.

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An autosomal transcript in skeletal muscle with homology to dystrophin von Love, Donald R., Hill, Diane F., Dickson, George, Spurr, Nigel K., Byth, Barbara C., Marsden, Rosalind F., Walsh, Frank S., Edwards, Yvonne H., Davies, Kay E.

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The utrophin and dystrophin genes share similarities in genomic structure von Pearce, Marcela, Blake, Derek J., Tinsley, Jonathon M., Byth, Barbara C., Campbell, Louise, Monaco, Anthony P., Davies, Kay E.

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A (CA)n repeat polymorphism near the 3' end to the CBG gene von BYTH, B. C, COX, D. W

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Application of inverse PCR to isolation of end probes from cosmids von Byth, Barbara C., Thomas, Gordon R., Hofland, Nandy, Cox, Diane W.

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Polymorphism of the protein C inhibitor (PCI) gene on chromosome 14 von Ashbourne, Katherine J., Byth, Barbara C., Meijers, Joost C.M., Cox, Diane W.

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A new DNA marker, D6S129, identifies a HindIII polymorphism on chromosome 6q von BYTH, B. C, LOVE, D. R, PASSOS-BUENO, M. R, DAVIES, K. E

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Molecular analysis of three patients with interstitial deletions of chromosome band 14q31 von Byth, B C, Costa, M T, Teshima, I E, Wilson, W G, Carter, N P, Cox, D W

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A (CA)n repeat polymorphism in the protein C inhibitor (PCI) gene von Byth, Barbara C., Meijers, Joost C.M., Cox, Diane W.

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Dystrophin and dystrophin-related proteins: A review of protein and RNA studies von Love, Donald R., Byth, Barbara C., Tinsley, Jonathon M., Blake, Derek J., Davies, Kay E.

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Physical and genetic mapping of the serpin gene cluster at 14q32.1: allelic association and a unique haplotype associated with alpha 1-antitrypsin deficiency von Byth, B C, Billingsley, G D, Cox, D W

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Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: Intragenic heterogeneity or a new form of X-linked mental retardation? von Passos-Bueno, Maria Rita, Byth, Barbara C., Rosenberg, Sergio, Takata, Reinaldo I., Bakker, Egbert, Beggs, Alan H., Pavanello, Rita C., Vainzof, Mariz, Davies, Kay E., Zatz, Mayana

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Physical and genetic mapping of the serpin gene cluster at 14q32.1 : allelic association and a unique haplotype associated with α1-antitrypsin deficiency von BYTH, B. C, BILLINGSLEY, G. D, COX, D. W

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Two consecutive dinucleotide repeats constitute an informative marker at the α1-antichymotrypsin (AACT) locus von Byth, Barbara C., Cox, Diane W.

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A (CA)n repeat polymorphism at the 5′ end of the α1antitrypsin gene (PI) von Byth, Barbara C., Cox, Diane W.

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A (CA)n repeat polymorphism at the 5' end of the alpha 1-antitrypsin gene (PI) von Byth, B C, Cox, D W

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Two consecutive dinucleotide repeats constitute an informative marker at the alpha 1-antichymotrypsin (AACT) locus von Byth, B C, Cox, D W

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A new DNA marker, D6S129, identifies a Hindlll polymorphism On ChromoSome 6q von Byth, B.C., Love, D.R., Passos-Bueno, M.R., Davies, K.E.

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Evaluation of a peer education program on student leaders' energy balance-related behaviors von Foley, B C, Shrewsbury, V A, Hardy, L L, Flood, V M, Byth, K, Shah, S

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