Connection

G. Pai to Syndrome

This is a "connection" page, showing publications G. Pai has written about Syndrome.
Connection Strength

0.108
  1. Diagnostic approach to children with birth defects. Indian J Pediatr. 2000 Nov; 67(11):819-23.
    View in: PubMed
    Score: 0.042
  2. Alstr?m syndrome: a case misdiagnosed as Bardet-Biedl syndrome. J Pediatr Ophthalmol Strabismus. 1994 Jul-Aug; 31(4):272-4.
    View in: PubMed
    Score: 0.027
  3. Bleomycin hypersensitivity in dyskeratosis congenita fibroblasts, lymphocytes, and transformed lymphoblasts. Cytogenet Cell Genet. 1989; 52(3-4):186-9.
    View in: PubMed
    Score: 0.019
  4. A new Seckel-like syndrome of primordial dwarfism. Am J Med Genet. 1996 Aug 23; 64(3):447-52.
    View in: PubMed
    Score: 0.008
  5. Walker-Warburg syndrome: report of three affected sibs. Am J Med Genet. 1994 Jan 15; 49(2):198-201.
    View in: PubMed
    Score: 0.007
  6. Heterozygote detection through bleomycin-induced G2 chromatid breakage in dyskeratosis congenita families. Cancer Genet Cytogenet. 1992 May; 60(1):31-4.
    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.