Improved diagnosis of Duchenne/Becker muscular dystrophy.

per Beggs, A H, Kunkel, L M
Publicat 1990

Chromatin loop structure of the human X chromosome: relevance to X inactivation and CpG clusters.

per Beggs, A H, Migeon, B R
Publicat 1989

Exclusion of two candidate loci for autosomal recessive nemaline myopathy.

per Tahvanainen, E, Beggs, A H, Wallgren-Pettersson, C
Publicat 1994

Extinction of JC virus tumor-antigen expression in glial cell--fibroblast hybrids.

per Beggs, A H, Frisque, R J, Scangos, G A
Publicat 1988

Dystrophin is transcribed in brain from a distant upstream promoter.

per Boyce, F M, Beggs, A H, Feener, C, Kunkel, L M
Publicat 1991

A gene for isolated congenital ptosis maps to a 3-cM region within 1p32-p34.1.

per Engle, E C, Castro, A E, Macy, M E, Knoll, J H, Beggs, A H
Publicat 1997

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy.

per Beggs, A H, Neumann, P E, Arahata, K, Arikawa, E, Nonaka, I, Anderson, M S, Kunkel, L M
Publicat 1992

Congenital fibrosis of the extraocular muscles type 2, an inherited exotropic strabismus fixus, maps to distal 11q13.

per Wang, S M, Zwaan, J, Mullaney, P B, Jabak, M H, Al-Awad, A, Beggs, A H, Engle, E C
Publicat 1998

Clinical Phenotype of X‐Linked Myotubular Myopathy in Labrador Retriever Puppies

per Snead, E.C.R., Taylor, S.M., van der Kooij, M., Cosford, K., Beggs, A.H., Shelton, G.D.
Publicat a J Vet Intern Med (2015)

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

per Beggs, A H, Hoffman, E P, Snyder, J R, Arahata, K, Specht, L, Shapiro, F, Angelini, C, Sugita, H, Kunkel, L M
Publicat 1991

Congenital fibrosis of the extraocular muscles (autosomal dominant congenital external ophthalmoplegia): genetic homogeneity, linkage refinement, and physical mapping on chromosome...

per Engle, E C, Marondel, I, Houtman, W A, de Vries, B, Loewenstein, A, Lazar, M, Ward, D C, Kucherlapati, R, Beggs, A H
Publicat 1995

Large duplication in MTM1 associated with myotubular myopathy

per Amburgey, K., Lawlor, M.W., del Gaudio, D., Cheng, Y.W., Fitzpatrick, C., Minor, A., Li, X., Aughton, D., Das, S., Beggs, A.H., Dowling, J.J.
Publicat 2012

Dystrophin analysis in idiopathic dilated cardiomyopathy.

per Michels, V V, Pastores, G M, Moll, P P, Driscoll, D J, Miller, F A, Burnett, J C, Rodeheffer, R J, Tajik, J A, Beggs, A H, Kunkel, L M
Publicat 1993

Congenital myopathy caused by a novel missense mutation in the CFL2 gene

per Ockeloen, C.W., Gilhuis, H.J., Pfundt, R., Kamsteeg, E.J., Agrawal, P.B., Beggs, A.H., Hama-Amin, A. Dara, Diekstra, A., Knoers, N.V.A.M., Lammens, M., van Alfen, N.
Publicat 2012

Functional muscle analysis of the Tcap knockout mouse

per Markert, C.D., Meaney, M.P., Voelker, K.A., Grange, R.W., Dalley, H.W., Cann, J.K., Ahmed, M., Bishwokarma, B., Walker, S.J., Yu, S.X., Brown, M., Lawlor, M.W., Beggs, A.H., Childers, M.K.
Publicat 2010

Assignment of a gene (NEM1) for autosomal dominant nemaline myopathy to chromosome 1

per Laing, N. G., Majda, B. T., Akkari, P. A., Layton, M. G., Mulley, J. C., Phillips, H., Haan, E. A., White, S. J., Beggs, A. H., Kunkel, L. M., Groth, D. M., Boundy, K. L., Kneebone, C. S., Blumberg, P. C., Wilton, S. D., Speer, M. C., Kakulas, B. A.
Publicat 1992

Dysfunctional sarcomere contractility contributes to muscle weakness in ACTA1-related nemaline myopathy (NEM3)

per Joureau, B., de Winter, J.M., Conijn, S., Bogaards, S.J.P., Kovacevic, I., Kalganov, A., Persson, M., Lindqvist, J., Stienen, G.J.M., Irving, T.C., Ma, W., Yuen, M., Clarke, N.F., Rassier, D.E., Malfatti, E., Romero, N.B., Beggs, A.H., Ottenheijm, C.A.C
Publicat a Ann Neurol (2018)

The molecular basis for Duchenne versus Becker muscular dystrophy: Correlation of severity with type of deletion

per Koenig, M., Beggs, A. H., Moyer, M., Scherpf, S., Heindrich, K., Bettecken, T., Meng, G., Müller, C. R., Lindlöf, M., Kaariainen, H., de la Chapelle, A., Kiuru, A., Savontaus, M.-L., Gilgenkrantz, H., Récan, D., Chelly, J., Kaplan, J.-C., Covone, A. E., Archidiacono, N., Romeo, G., Liechti-Gallati, S., Schneider, V., Braga, S., Moser, H., Darras, B. T., Murphy, P., Francke, U., Chen, J. D., Morgan, G., Denton, M., Greenberg, C. R., Wrogemann, K., Blonden, L. A. J., van Paassen, H. M. B., van Ommen, G. J. B., Kunkel, L. M.
Publicat 1989

Patient-Customized Oligonucleotide Therapy for a Rare Genetic Disease

per Kim, J., Hu, C., Moufawad El Achkar, C., Black, L.E., Douville, J., Larson, A., Pendergast, M.K., Goldkind, S.F., Lee, E.A., Kuniholm, A., Soucy, A., Vaze, J., Belur, N.R., Fredriksen, K., Stojkovska, I., Tsytsykova, A., Armant, M., DiDonato, R.L., Choi, J., Cornelissen, L., Pereira, L.M., Augustine, E.F., Genetti, C.A., Dies, K., Barton, B., Williams, L., Goodlett, B.D., Riley, B.L., Pasternak, A., Berry, E.R., Pflock, K.A., Chu, S., Reed, C., Tyndall, K., Agrawal, P.B., Beggs, A.H., Grant, P.E., Urion, D.K., Snyder, R.O., Waisbren, S.E., Poduri, A., Park, P.J., Patterson, A., Biffi, A., Mazzulli, J.R., Bodamer, O., Berde, C.B., Yu, T.W.
Publicat a N Engl J Med (2019)