Stratton RF - Search Results

1

Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.

Probst FJ, Roeder ER, Enciso VB, Ou Z, Cooper ML, Eng P, Li J, Gu Y, Stratton RF, Chinault AC, Shaw CA, Sutton VR, Cheung SW, Nelson DL. Probst FJ, et al. Among authors: stratton rf. Am J Med Genet A. 2007 Jun 15;143A(12):1358-65. doi: 10.1002/ajmg.a.31781. Am J Med Genet A. 2007. PMID: 17506108

2

Metastatic medulloblastoma in an adolescent with Simpson-Golabi-Behmel syndrome.

Thomas M, Enciso V, Stratton R, Shah S, Winder T, Tayeh M, Roeder E. Thomas M, et al. Am J Med Genet A. 2012 Oct;158A(10):2534-6. doi: 10.1002/ajmg.a.35284. Epub 2012 Aug 14. Am J Med Genet A. 2012. PMID: 22893378

3

Deletion (2)(q37).

Stratton RF, Tolworthy JA, Young RS. Stratton RF, et al. Am J Med Genet. 1994 Jun 1;51(2):153-5. doi: 10.1002/ajmg.1320510215. Am J Med Genet. 1994. PMID: 8092193 Review.

4

Deletion of the proximal short arm of chromosome 8.

Stratton RF, Crudo DF, Varela M, Shapira E. Stratton RF, et al. Am J Med Genet. 1992 Jan 1;42(1):15-8. doi: 10.1002/ajmg.1320420105. Am J Med Genet. 1992. PMID: 1308359

5

Frontonasal malformation with tetralogy of Fallot associated with a submicroscopic deletion of 22q11.

Stratton RF, Payne RM. Stratton RF, et al. Am J Med Genet. 1997 Mar 31;69(3):287-9. doi: 10.1002/(sici)1096-8628(19970331)69:3<287::aid-ajmg13>3.0.co;2-n. Am J Med Genet. 1997. PMID: 9096758

6

Deletion 5q35.3.

Stratton RF, Tedrowe NA, Tolworthy JA, Patterson RM, Ryan SG, Young RS. Stratton RF, et al. Am J Med Genet. 1994 Jun 1;51(2):150-2. doi: 10.1002/ajmg.1320510214. Am J Med Genet. 1994. PMID: 8092192

7

Interstitial duplication of 7(q22-->q34).

Stratton RF, DuPont BR, Mattern VL, Schelonka RL, Moore CM. Stratton RF, et al. Am J Med Genet. 1993 Sep 1;47(3):380-2. doi: 10.1002/ajmg.1320470316. Am J Med Genet. 1993. PMID: 8135285

8

Deletion (11)(q14.1q21).

Stratton RF, Lazarus KH, Ritchie EJ, Bell AM. Stratton RF, et al. Am J Med Genet. 1994 Feb 1;49(3):294-8. doi: 10.1002/ajmg.1320490310. Am J Med Genet. 1994. PMID: 7516119 Review.

9

Interstitial duplication 19p.

Stratton RF, DuPont BR, Olsen AS, Fertitta A, Hoyer M, Moore CM. Stratton RF, et al. Am J Med Genet. 1995 Jul 17;57(4):562-4. doi: 10.1002/ajmg.1320570409. Am J Med Genet. 1995. PMID: 7573129

10

Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay.

Cody JD, Sebold C, Malik A, Heard P, Carter E, Crandall A, Soileau B, Semrud-Clikeman M, Cody CM, Hardies LJ, Li J, Lancaster J, Fox PT, Stratton RF, Perry B, Hale DE. Cody JD, et al. Among authors: stratton rf. Am J Med Genet A. 2007 Jun 1;143A(11):1181-90. doi: 10.1002/ajmg.a.31729. Am J Med Genet A. 2007. PMID: 17486614 Free article.

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