Connection

G. Pai to In Situ Hybridization, Fluorescence

This is a "connection" page, showing publications G. Pai has written about In Situ Hybridization, Fluorescence.
Connection Strength

0.071
  1. An atypical Turner syndrome patient with ring X chromosome mosaicism. Ann Clin Lab Sci. 1995 Jan-Feb; 25(1):60-5.
    View in: PubMed
    Score: 0.030
  2. Fluorescence in situ hybridization (FISH) of a whole-arm translocation involving chromosomes 18 and 20 with alpha-satellite DNA probes: detection of a centromeric DNA break? Am J Med Genet. 1992 Oct 01; 44(3):340-4.
    View in: PubMed
    Score: 0.025
  3. Xp pseudoautosomal gene haploinsufficiency and linear growth deficiency in three girls with chromosome Xp22;Yq11 translocation. J Med Genet. 1996 Nov; 33(11):906-11.
    View in: PubMed
    Score: 0.008
  4. Molecular analysis of a complex chromosomal rearrangement and a review of familial cases. Am J Med Genet. 1994 Nov 15; 53(3):255-63.
    View in: PubMed
    Score: 0.007
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.