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A marker X chromosome.
PMID: 5794013 [PubMed - indexed for MEDLINE]
PMCID: PMC1706424
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Cited by 52 PubMed Central articles
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Mendelian Inheritance in Man and its online version, OMIM.
McKusick VA.
Am J Hum Genet. 2007 Apr; 80(4):588-604. Epub 2007 Mar 8.
[Am J Hum Genet. 2007]
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Allan-Herndon-Dudley syndrome and the monocarboxylate transporter 8 (MCT8) gene.
Schwartz CE, May MM, Carpenter NJ, Rogers RC, Martin J, Bialer MG, Ward J, Sanabria J, Marsa S, Lewis JA, et al.
Am J Hum Genet. 2005 Jul; 77(1):41-53. Epub 2005 May 11.
[Am J Hum Genet. 2005]
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Renpenning syndrome maps to Xp11.
Stevenson RE, Arena JF, Ouzts E, Gibson A, Shokeir MH, Vnencak-Jones C, Lubs HA, May M, Schwartz CE.
Am J Hum Genet. 1998 May; 62(5):1092-101.
[Am J Hum Genet. 1998]
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