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        - 2024
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                        Mark
        A genomic mutational constraint map using variation in 76,156 human genomes
    
    
- Contribution to journal › Article
 
 - 2022
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                        Mark
        Multi-Omic Investigations of a 17-19 Translocation Links MINK1 Disruption to Autism, Epilepsy and Osteoporosis
    
    
- Contribution to journal › Article
 
 - 2012
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                        Mark
        Characterization of mutations in barley fch2 encoding chlorophyllide a oxygenase
    
    
- Contribution to journal › Article
 
 - 2008
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                        Mark
        An investigation into whether deletions in 9p reflect prognosis in adult precursor B-cell acute lymphoblastic leukemia : a multi-center study of 381 patients
    
    
- Contribution to journal › Article
 
 - 2006
 - 
                        Mark
        Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia
    
    
- Contribution to journal › Article
 
 - 2005
 - 
                        Mark
        Interspecies synteny mapping identifies a quantitative trait locus for bone mineral density on human chromosome Xp22
    
    
- Contribution to journal › Article
 
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                        Mark
        Genetic dissection of neurodegeneration and CNS inflammation
    
    
- Contribution to journal › Article
 
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                        Mark
        A manually curated functional annotation of the human X chromosome
    
    
- Contribution to journal › Letter
 
 - 2004
 - 
                        Mark
        Amplification of chromosome 1 sequences in lipomatous tumors and other sarcomas
    
    
- Contribution to journal › Article
 
 - 2003
 - 
                        Mark
        Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
    
    
- Contribution to journal › Article
 
 
