Connection

DAVID NELSON to In Situ Hybridization, Fluorescence

This is a "connection" page, showing publications DAVID NELSON has written about In Situ Hybridization, Fluorescence.
  1. Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation. Am J Med Genet A. 2007 Jun 15; 143A(12):1358-65.
    View in: PubMed
    Score: 0.062
  2. The human secretin gene: fine structure in 11p15.5 and sequence variation in patients with autism. Genomics. 2002 Aug; 80(2):185-94.
    View in: PubMed
    Score: 0.044
  3. Molecular definition of pericentric inversion breakpoints occurring during the evolution of humans and chimpanzees. Genomics. 1998 Jun 15; 50(3):368-72.
    View in: PubMed
    Score: 0.033
  4. Desmoplakin and talin2 are novel mRNA targets of fragile X-related protein-1 in cardiac muscle. Circ Res. 2011 Jul 22; 109(3):262-71.
    View in: PubMed
    Score: 0.020
  5. A mutation in human CMP-sialic acid hydroxylase occurred after the Homo-Pan divergence. Proc Natl Acad Sci U S A. 1998 Sep 29; 95(20):11751-6.
    View in: PubMed
    Score: 0.008
  6. Large domains of apparent delayed replication timing associated with triplet repeat expansion at FRAXA and FRAXE. Am J Hum Genet. 1996 Aug; 59(2):407-16.
    View in: PubMed
    Score: 0.007
  7. The gene encoding the VP16-accessory protein HCF (HCFC1) resides in human Xq28 and is highly expressed in fetal tissues and the adult kidney. Genomics. 1995 Jan 20; 25(2):462-8.
    View in: PubMed
    Score: 0.007
  8. High-resolution mapping of probes near the X-linked lymphoproliferative disease (XLP) locus. Genomics. 1993 Jul; 17(1):163-70.
    View in: PubMed
    Score: 0.006
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

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