Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.
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A. Ballabio | M. Rafiq | P. Aridon | G. Casari | W. Ahmad | B. Franco | M. Amin-ud-din | M. Faiyaz ul Haque | S. ul Haque | M. Ahmad | T. Sarno | S. Noci | M. De Fusco | S. Ul Haque
[1] C. Walsh,et al. Missense mutation in PAK3, R67C, causes X-linked nonspecific mental retardation. , 2000, American journal of medical genetics.
[2] J. Gécz,et al. Genes for cognitive function: developments on the X. , 2000, Genome research.
[3] A. Meindl,et al. A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation , 2000, Nature Genetics.
[4] J Liu,et al. Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation. , 1999, Genomics.
[5] R. Stevenson,et al. Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel. , 1999, Genomics.
[6] Lin Jun,et al. A new member of the IL-1 receptor family highly expressed in hippocampus and involved in X-linked mental retardation , 1999, Nature Genetics.
[7] J. Gécz,et al. A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation , 1999, Nature Genetics.
[8] H. Lubs,et al. XLMR genes: update 1998. , 1999, American journal of medical genetics.
[9] C. Walsh,et al. PAK3 mutation in nonsyndromic X-linked mental retardation , 1998, Nature Genetics.
[10] Andrea Menegon,et al. Mutations in GDI1 are responsible for X-linked non-specific mental retardation , 1998, Nature Genetics.
[11] H. R. Crollius,et al. Oligophrenin-1 encodes a rhoGAP protein involved in X-linked mental retardation , 1998, Nature.
[12] I. Scheffer,et al. doublecortin , a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein , 1998, Cell.
[13] Y. Berwald‐Netter,et al. A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome , 1998, Cell.
[14] K. Dry,et al. Analysis of three deletion breakpoints in Xp21.1 and the further localization of RP3. , 1996, Genomics.
[15] A. Donnelly,et al. How many X-linked genes for non-specific mental retardation (MRX) are there? , 1996, American journal of medical genetics.
[16] J. Gécz,et al. Identification of the gene FMR2, associated with FRAXE mental retardation , 1996, Nature Genetics.
[17] R. Gibbs,et al. Identification of FMR2, a novel gene associated with the FRAXE CCG repeat and CpG island , 1996, Nature Genetics.
[18] P. Marynen,et al. Localisation of a new gene for non-specific mental retardation to Xq22-q26 (MRX35). , 1996, Journal of medical genetics.
[19] H. Lubs,et al. XLMR genes: update 1990. , 1991, American journal of medical genetics.
[20] J. Ott,et al. Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.
[21] J. Chelly. Breakthroughs in molecular and cellular mechanisms underlying X-linked mental retardation. , 1999, Human molecular genetics.