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May 1, 2010Journal of Medical Genetics

Further molecular and clinical delineation of co-locating 17p13.3 microdeletions and microduplications that show distinctive phenotypes

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Authors

DBDamien L. BrunoGallaudet UniversityBABritt‐Marie AnderlidKarolinska University HospitalALAnna LindstrandKarolinska University Hospital

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Cite This Study

Bruno et al. (2010) studied this question.

synapsesocial.com/papers/6a88359886ac178e8f608f16https://doi.org/10.1136/jmg.2009.069906
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Also Consider

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  1. 1Mapping of a Novel Ocular and Cutaneous Malignant Melanoma Susceptibility Locus to Chromosome 9q21.322005 · 63 citations
  2. 2A new microduplication syndrome encompassing the region of the Miller–Dieker (17p13 deletion) syndrome2009 · 113 citations
  3. 3High frequency of genomic deletions—and a duplication—in the LIS1 gene in lissencephaly: implications for molecular diagnosis2008 · 52 citations