Genetic and Physical Mapping at the Limb-Girdle Muscular Dystrophy Locus (LGMD2B) on Chromosome 2p

By Bashir R.   Keers S.   Strachan T.   Passos-Bueno R.   Zatz M.   Weissenbach J.   Le Paslier D.   Meisler M.   Bushby K.  

Genomics, Vol. 33, Iss. 1, 1996-04 ,pp. : 46-52

Academic Press

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A Gene for Autosomal Dominant Progressive Cone Dystrophy (CORD5) Maps to Chromosome 17p12–p13

By Balciuniene J.   Johansson K.   Sandgren O.   Wachtmeister L.   Holmgren G.   Kristina Forsman A.  

Genomics, Vol. 30, Iss. 2, 1995-11 ,pp. : 281-286

Academic Press

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A Fine Integrated Map of the SPG4 Locus Excludes an Expanded CAG Repeat in Chromosome 2p-Linked Autosomal Dominant Spastic Paraplegia

By Hazan J.   Davoine C.-S.   Mavel D.   Fonknechten N.   Paternotte C.   Fizames C.   Cruaud C.   Samson D.   Muselet D.   Vega-Czarny N.   Brice A.   Gyapay G.   Heilig R.   Fontaine B.   Weissenbach J.  

Genomics, Vol. 60, Iss. 3, 1999-09 ,pp. : 309-319

Elsevier

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Generation of a 3-Mb PAC Contig Spanning the Miyoshi Myopathy/Limb-Girdle Muscular Dystrophy (MM/LGMD2B) Locus on Chromosome 2p13

By Liu J.   Wu C.   Bossie K.   Bejaoui K.   Hosler B.A.   Gingrich J.C.   Hamida M.B.   Hentati F.   Schurr E.   de Jong P.J.   Brown R.H.  

Genomics, Vol. 49, Iss. 1, 1998-04 ,pp. : 23-29

Elsevier

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FRG1, a gene in the FSH muscular dystrophy region on human chromosome 4q35, is highly conserved in vertebrates and invertebrates

By Grewal P.K.   Carim Todd L.   van der Maarel S.   Frants R.R.   Hewitt J.E.  

Gene, Vol. 216, Iss. 1, 1998-08 ,pp. : 13-19

Elsevier

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