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

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

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

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

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

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

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

An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus. by 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. by Kunkel, L, Monaco, A, Middlesworth, W, Ochs, H, Latt, SA

THE GIANT DUCHENNE MUSCULAR-DYSTROPHY GENE AND ITS PROTEIN PRODUCT by 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. by Kunkel, L, Lalande, M, Monaco, A, Flint, A, Middlesworth, W, Latt, SA

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

Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. by 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. by Monaco, A, Neve, R, Colletti-Feener, C, Bertelson, C, Kurnit, D, Kunkel, L

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

DNA linkage analysis of X chromosome-linked chronic granulomatous disease. by 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. by 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. by 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. by Burmeister, M, Monaco, A, Gillard, E, van Ommen, G, Affara, N, Ferguson-Smith, M, Kunkel, L, Lehrach, H