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Connection

Shawn McCandless to Chromosome Deletion

This is a "connection" page, showing publications Shawn McCandless has written about Chromosome Deletion.

 
Connection Strength
 
 
 
0.652
 
  1. Quigley DI, Sailus J, Kaiser-Rogers K, Rao KW, Calikoglu M, Gold S, McCandless SE. A clinical report of a patient with two abnormal cell lines: 46,XX,del(21)(q22.1) and 47,XX,+3. Am J Med Genet A. 2005 Jan 01; 132A(1):101-5.
    View in: PubMed
    Score: 0.237
  2. McCandless SE, Schwartz S, Morrison S, Garlapati K, Robin NH. Adult with an interstitial deletion of chromosome 10 [del(10)(q25. 1q25.3)]: overlap with Coffin-Lowry syndrome. Am J Med Genet. 2000 Nov 13; 95(2):93-8.
    View in: PubMed
    Score: 0.178
  3. McCandless SE, Scott JA, Robin NH. Deletion 22q11: a newly recognized cause of behavioral and psychiatric disorders. Arch Pediatr Adolesc Med. 1998 May; 152(5):481-4.
    View in: PubMed
    Score: 0.149
  4. Al-Kateb H, Hahn A, Gastier-Foster JM, Jeng L, McCandless SE, Curtis CA. Molecular characterization of a novel, de novo, cryptic interstitial deletion on 19p13.3 in a child with a cutis aplasia and multiple congenital anomalies. Am J Med Genet A. 2010 Dec; 152A(12):3148-53.
    View in: PubMed
    Score: 0.089
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.

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