Connection

JIMMY HOLDER JR to In Situ Hybridization, Fluorescence

This is a "connection" page, showing publications JIMMY HOLDER JR has written about In Situ Hybridization, Fluorescence.
  1. Refinement of the postnatal growth restriction locus of chromosome 5q12-13 deletion syndrome. Am J Med Genet A. 2015 Nov; 167A(11):2737-41.
    View in: PubMed
    Score: 0.102
  2. A child with an inherited 0.31?Mb microdeletion of chromosome 14q32.33: further delineation of a critical region for the 14q32 deletion syndrome. Am J Med Genet A. 2012 Aug; 158A(8):1962-6.
    View in: PubMed
    Score: 0.082
  3. Profound obesity associated with a balanced translocation that disrupts the SIM1 gene. Hum Mol Genet. 2000 Jan 01; 9(1):101-8.
    View in: PubMed
    Score: 0.035
  4. Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27. Eur J Hum Genet. 2015 Jan; 23(1):54-60.
    View in: PubMed
    Score: 0.024
Connection Strength

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Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.