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Carl Dobkin

Prince of Songkla University

22

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1224

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Identification of fragile X syndrome specific molecular markers in human fibroblasts: a useful model to test the efficacy of therapeutic drugs.

2014 Human Mutation
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Fragile X protein in newborn dried blood spots

2014 BMC Medical Genetics
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Fragile X AGG analysis provides new risk predictions for 45-69 repeat alleles.

2013 American Journal of Medical Genetics Part A
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A 5-methylcytosine hotspot responsible for the prevalent HSD17B10 mutation

2013 Gene
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Terminal deletions of the long arm of chromosome X that include the FMR1 gene in female patients: a case series.

2011 American Journal of Medical Genetics Part A
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Tissue and developmental regulation of fragile X mental retardation 1 exon 12 and 15 isoforms

2009 Neurobiology of Disease
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Fmr1 knockout mouse has a distinctive strain-specific learning impairment.

2000 Neuroscience
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FMR1 CGG-Repeat Instability in Single Sperm and Lymphocytes of Fragile-X Premutation Males

1999 American Journal of Human Genetics
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Single cell analysis shows different FMR1 CGG repeat stability in sperm and lymphocytes of premutation males

1997
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Polymorphism of FXR1 showing lack of association with autism

1997 American Journal of Medical Genetics
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Citations (6)