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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1992 | 1 |
1993 | 1 |
1994 | 1 |
1999 | 1 |
2011 | 1 |
2024 | 0 |
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Molecular cloning and characterization of TRPC5 (HTRP5), the human homologue of a mouse brain receptor-activated capacitative Ca2+ entry channel.
Genomics. 1999 Sep 15;60(3):330-40. doi: 10.1006/geno.1999.5924.
Genomics. 1999.
PMID: 10493832
Deletion of the immunoglobulin domain of IL1RAPL1 results in nonsyndromic X-linked intellectual disability associated with behavioral problems and mild dysmorphism.
Franek KJ, Butler J, Johnson J, Simensen R, Friez MJ, Bartel F, Moss T, DuPont B, Berry K, Bauman M, Skinner C, Stevenson RE, Schwartz CE.
Franek KJ, et al.
Am J Med Genet A. 2011 May;155A(5):1109-14. doi: 10.1002/ajmg.a.33833. Epub 2011 Apr 11.
Am J Med Genet A. 2011.
PMID: 21484992
Item in Clipboard
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
Item in Clipboard
MRX8: an X-linked mental retardation condition with linkage to Xq21.
Schwartz CE, May M, Huang T, Ledbetter D, Anderson G, Barker DF, Lubs HA, Arena F, Stevenson RE.
Schwartz CE, et al.
Am J Med Genet. 1992 Apr 15-May 1;43(1-2):467-74. doi: 10.1002/ajmg.1320430170.
Am J Med Genet. 1992.
PMID: 1605227
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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.
Clin Dysmorphol. 1993 Oct;2(4):332-41.
Clin Dysmorphol. 1993.
PMID: 8305964
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