Stevenson RE - Search Results

1

The impact of spermine synthase (SMS) mutations on brain morphology.

Kesler SR, Schwartz C, Stevenson RE, Reiss AL. Kesler SR, et al. Among authors: stevenson re. Neurogenetics. 2009 Oct;10(4):299-305. doi: 10.1007/s10048-009-0184-2. Epub 2009 Mar 7. Neurogenetics. 2009. PMID: 19277733 Free PMC article.

2

Allan-Herndon syndrome. I. Clinical studies.

Stevenson RE, Goodman HO, Schwartz CE, Simensen RJ, McLean WT Jr, Herndon CN. Stevenson RE, et al. Am J Hum Genet. 1990 Sep;47(3):446-53. Am J Hum Genet. 1990. PMID: 2393019 Free PMC article.

3

Allan-Herndon syndrome. II. Linkage to DNA markers in Xq21.

Schwartz CE, Ulmer J, Brown A, Pancoast I, Goodman HO, Stevenson RE. Schwartz CE, et al. Among authors: stevenson re. Am J Hum Genet. 1990 Sep;47(3):454-8. Am J Hum Genet. 1990. PMID: 2393020 Free PMC article.

4

Agenesis of the corpus callosum associated with MASA syndrome.

Boyd E, Schwartz CE, Schroer RJ, May MM, Shapiro SD, Arena JF, Lubs HA, Stevenson RE. Boyd E, et al. Among authors: stevenson re. Clin Dysmorphol. 1993 Oct;2(4):332-41. Clin Dysmorphol. 1993. PMID: 8305964

5

Differences in methylenetetrahydrofolate reductase genotype frequencies, between Whites and Blacks.

Stevenson RE, Schwartz CE, Du YZ, Adams MJ Jr. Stevenson RE, et al. Am J Hum Genet. 1997 Jan;60(1):229-30. Am J Hum Genet. 1997. PMID: 8981967 Free PMC article. No abstract available.

6

Arch fingerprints, hypotonia, and areflexia associated with X linked mental retardation.

Stevenson RE, Häne B, Arena JF, May M, Lawrence L, Lubs HA, Schwartz CE. Stevenson RE, et al. J Med Genet. 1997 Jun;34(6):465-9. doi: 10.1136/jmg.34.6.465. J Med Genet. 1997. PMID: 9192265 Free PMC article.

7

Renpenning syndrome maps to Xp11.

Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE. Stevenson RE, et al. Am J Hum Genet. 1998 May;62(5):1092-101. doi: 10.1086/301835. Am J Hum Genet. 1998. PMID: 9545405 Free PMC article.

8

X-linked mental retardation syndrome with seizures, hypogammaglobulinemia, and progressive gait disturbance is regionally mapped between xq21.33 and Xq23.

Chudley AE, Tackels DC, Lubs HA, Arena JF, Stoeber WP, Kovnats S, Stevenson RE, Schwartz CE. Chudley AE, et al. Among authors: stevenson re. Am J Med Genet. 1999 Jul 30;85(3):255-62. doi: 10.1002/(sici)1096-8628(19990730)85:3<255::aid-ajmg14>3.0.co;2-z. Am J Med Genet. 1999. PMID: 10398239

9

A new X linked mental retardation (XLMR) syndrome with short stature, small testes, muscle wasting, and tremor localises to Xq24-q25.

Cabezas DA, Slaugh R, Abidi F, Arena JF, Stevenson RE, Schwartz CE, Lubs HA. Cabezas DA, et al. Among authors: stevenson re. J Med Genet. 2000 Sep;37(9):663-8. doi: 10.1136/jmg.37.9.663. J Med Genet. 2000. PMID: 10978355 Free PMC article.

10

Holmes-Gang syndrome is allelic with XLMR-hypotonic face syndrome.

Stevenson RE, Abidi F, Schwartz CE, Lubs HA, Holmes LB. Stevenson RE, et al. Am J Med Genet. 2000 Oct 23;94(5):383-5. doi: 10.1002/1096-8628(20001023)94:5<383::aid-ajmg7>3.0.co;2-7. Am J Med Genet. 2000. PMID: 11050622 No abstract available.

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