نتائج البحث - P.A.L. Wight
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X chromosome-linked muscular dystrophy (mdx) in the mouse. حسب G. Bulfield, W. G. Siller, P.A.L. Wight, Karen J. Moore
منشور في 1984Artigo -
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Xq22 deletions and correlation with distinct neurological disease traits in females: Further evidence for a contiguous gene syndrome حسب Hadia Hijazi, Fernanda S. Coelho, Claudia Gonzaga‐Jauregui, Laura Bernardini, Soe Mar, Melanie A. Manning, Andrea Hanson‐Kahn, SakkuBai Naidu, Siddharth Srivastava, Jennifer A. Lee, Julie R. Jones, Michael J. Friez, Thomas Alberico, Bárbara Torres, Ping Fang, Sau Wai Cheung, Xiaofei Song, Angelique Davis‐Williams, Carly Jornlin, P.A.L. Wight, Pankaj Patyal, Jennifer R. Taube, Andrea Poretti, Ken Inoue, Feng Zhang, Davut Pehli̇van, Claudia M.B. Carvalho, Grace M. Hobson, James R. Lupski
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Molecular biology
Biochemistry
Candidate gene
Cell biology
Central nervous system
Chromosome
Chromosome 19
Chromosome 21
Comparative genomic hybridization
Creatine kinase
Duchenne muscular dystrophy
Endocrinology
Fusion gene
Fusion protein
Gene expression
Genetic linkage
Genetically modified mouse
Genome
Muscular dystrophy
Mutant
Myelin
Myelin basic protein
Myelin proteolipid protein
Neuroscience
Oligodendrocyte
Proteolipid protein 1
Recombinant DNA