Stevenson RE - Search Results

1

A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A.

Jiang YH, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL. Jiang YH, et al. Among authors: stevenson re. Am J Med Genet A. 2004 Nov 15;131(1):1-10. doi: 10.1002/ajmg.a.30297. Am J Med Genet A. 2004. PMID: 15389703

2

Duplication-deletion syndrome in a family with pericentric inversion of chromosome 6.

Schroer RJ, Culp DM, Stevenson RE, Potts WE, Taylor HA, Simensen RJ. Schroer RJ, et al. Among authors: stevenson re. Clin Genet. 1980 Jul;18(1):83-7. doi: 10.1111/j.1399-0004.1980.tb01369.x. Clin Genet. 1980. PMID: 7418257

3

Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome.

Stevenson RE, May M, Arena JF, Millar EA, Scott CI Jr, Schroer RJ, Simensen RJ, Lubs HA, Schwartz CE. Stevenson RE, et al. Am J Med Genet. 1994 Sep 1;52(3):339-45. doi: 10.1002/ajmg.1320520317. Am J Med Genet. 1994. PMID: 7810566

4

Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q.

Wang Y, Treat K, Schroer RJ, O'Brien JE, Stevenson RE, Schwartz CE. Wang Y, et al. Among authors: stevenson re. Am J Med Genet. 1994 Jun 1;51(2):169-75. doi: 10.1002/ajmg.1320510221. Am J Med Genet. 1994. PMID: 8092198

5

Nonsyndromic X-linked mental retardation: review and mapping of MRX29 to Xp21.

Häne B, Schroer RJ, Arena JF, Lubs HA, Schwartz CE, Stevenson RE. Häne B, et al. Among authors: stevenson re. Clin Genet. 1996 Oct;50(4):176-83. doi: 10.1111/j.1399-0004.1996.tb02622.x. Clin Genet. 1996. PMID: 9001795 Review.

6

Autism and macrocephaly.

Stevenson RE, Schroer RJ, Skinner C, Fender D, Simensen RJ. Stevenson RE, et al. Lancet. 1997 Jun 14;349(9067):1744-5. doi: 10.1016/S0140-6736(05)62956-X. Lancet. 1997. PMID: 9193390 No abstract available.

7

Autism and maternally derived aberrations of chromosome 15q.

Schroer RJ, Phelan MC, Michaelis RC, Crawford EC, Skinner SA, Cuccaro M, Simensen RJ, Bishop J, Skinner C, Fender D, Stevenson RE. Schroer RJ, et al. Among authors: stevenson re. Am J Med Genet. 1998 Apr 1;76(4):327-36. doi: 10.1002/(sici)1096-8628(19980401)76:4<327::aid-ajmg8>3.0.co;2-m. Am J Med Genet. 1998. PMID: 9545097

8

X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28.

Armfield K, Nelson R, Lubs HA, Häne B, Schroer RJ, Arena F, Schwartz CE, Stevenson RE. Armfield K, et al. Among authors: stevenson re. Am J Med Genet. 1999 Jul 30;85(3):236-42. doi: 10.1002/(sici)1096-8628(19990730)85:3<236::aid-ajmg10>3.0.co;2-9. Am J Med Genet. 1999. PMID: 10398235

9

Evidence that a dodecamer duplication in the gene HOPA in Xq13 is not associated with mental retardation.

Friez MJ, Essop FB, Krause A, Castiglia L, Ragusa A, Sossey-Alaoui K, Nelson RL, May MM, Michaelis RC, Srivastava AK, Schwartz CE, Stevenson RE, Goldman A, Villard L, Longshore JW. Friez MJ, et al. Among authors: stevenson re. Hum Genet. 2000 Jan;106(1):36-9. doi: 10.1007/s004390051006. Hum Genet. 2000. PMID: 10982179

10

The HOPA gene dodecamer duplication is not a significant etiological factor in autism.

Michaelis RC, Copeland-Yates SA, Sossey-Alaoui K, Skinner C, Friez MJ, Longshore JW, Simensen RJ, Schroer RJ, Stevenson RE. Michaelis RC, et al. Among authors: stevenson re. J Autism Dev Disord. 2000 Aug;30(4):355-8. doi: 10.1023/a:1005583517994. J Autism Dev Disord. 2000. PMID: 11039861

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