Cloning of the Duchenne/Becker muscular dystrophy locus. par Monaco, A, Kunkel, L

A GIANT LOCUS FOR THE DUCHENNE AND BECKER MUSCULAR-DYSTROPHY GENE par Monaco, A, Kunkel, L

The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein. par Koenig, M, Monaco, A, Kunkel, L

A small deletion in the Duchenne/Becker muscular dystrophy locus--a functionally important region? par Hart, K, Monaco, A, Kunkel, L, Bobrow, M

Molecular genetics of Duchenne muscular dystrophy. par Kunkel, L, Monaco, A, Bertelson, C, Colletti, C

Conservation of the Duchenne muscular dystrophy gene in mice and humans. par Hoffman, E, Monaco, A, Feener, C, Kunkel, L

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy. par Monaco, A, Bertelson, C, Colletti-Feener, C, Kunkel, L

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. par Monaco, A, Bertelson, C, Liechti-Gallati, S, Moser, H, Kunkel, L

Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. par Kunkel, L, Monaco, A, Middlesworth, W, Ochs, H, Latt, SA

THE GIANT DUCHENNE MUSCULAR-DYSTROPHY GENE AND ITS PROTEIN PRODUCT par Koenig, M, Hoffman, E, Monaco, A, Bertelson, C, Feener, C, Kunkel, L

Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci. par Kunkel, L, Lalande, M, Monaco, A, Flint, A, Middlesworth, W, Latt, SA

Molecular studies of progressive muscular dystrophy (Duchenne). par Kunkel, L, Monaco, A, Hoffman, E, Koenig, M, Feener, C, Bertelson, C

Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. par Koenig, M, Hoffman, E, Bertelson, C, Monaco, A, Feener, C, Kunkel, L

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. par Bertelson, C, Bartley, J, Monaco, A, Colletti-Feener, C, Fischbeck, K, Kunkel, L

Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene. par Monaco, A, Neve, R, Colletti-Feener, C, Bertelson, C, Kurnit, D, Kunkel, L

The Pathogenesis and Therapy of Muscular Dystrophies par Guiraud, S, Aartsma-Rus, A, Vieira, N, Davies, K, van Ommen, G, Kunkel, L

DNA linkage analysis of X chromosome-linked chronic granulomatous disease. par Baehner, R, Kunkel, L, Monaco, A, Haines, J, Conneally, P, Palmer, C, Heerema, N, Orkin, S

Cloning the gene for an inherited human disorder--chronic granulomatous disease--on the basis of its chromosomal location. par Royer-Pokora, B, Kunkel, L, Monaco, A, Goff, S, Newburger, P, Baehner, R, Cole, F, Curnutte, J, Orkin, S

Cloning the gene for the inherited disorder chronic granulomatous disease on the basis of its chromosomal location. par Royer-Pokora, B, Kunkel, L, Monaco, A, Goff, S, Newburger, P, Baehner, R, Cole, F, Curnutte, J, Orkin, S

A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene. par Burmeister, M, Monaco, A, Gillard, E, van Ommen, G, Affara, N, Ferguson-Smith, M, Kunkel, L, Lehrach, H