Connection

RICHARD KELLERMAYER to Abnormalities, Multiple

This is a "connection" page, showing publications RICHARD KELLERMAYER has written about Abnormalities, Multiple.
Connection Strength

0.739
  1. Upper gastrointestinal malformations in Coffin-Siris syndrome. Am J Med Genet A. 2007 Jul 01; 143A(13):1519-21.
    View in: PubMed
    Score: 0.185
  2. The versatile RECQL4. Genet Med. 2006 Apr; 8(4):213-6.
    View in: PubMed
    Score: 0.170
  3. Mos 46,XX,r(18).ish r(18)(18ptel-,18qtel-)/46,XX.ish del(18)(18ptel-): an example for successive ring chromosome formation. Am J Med Genet A. 2005 Dec 15; 139(3):234-5.
    View in: PubMed
    Score: 0.166
  4. Genotype-phenotype correlations in MYCN-related Feingold syndrome. Hum Mutat. 2008 Sep; 29(9):1125-32.
    View in: PubMed
    Score: 0.050
  5. Expanding the clinical spectrum of MYCN-related Feingold syndrome. Am J Med Genet A. 2006 Oct 15; 140(20):2254-6.
    View in: PubMed
    Score: 0.044
  6. Congenital chylothorax in Opitz G/BBB syndrome. Am J Med Genet A. 2006 May 15; 140(10):1119-21.
    View in: PubMed
    Score: 0.043
  7. Vertebral defects in a patient with Feingold syndrome. Clin Dysmorphol. 2005 Oct; 14(4):213-214.
    View in: PubMed
    Score: 0.041
  8. A patient with Rothmund-Thomson syndrome and all features of RAPADILINO. Arch Dermatol. 2005 May; 141(5):617-20.
    View in: PubMed
    Score: 0.040
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.