Publications

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2012
Celestino-Soper, PBS, Violante S, Crawford EL, Luo R, Lionel AC, Delaby E, Cai G, Sadikovic B, Lee K, Lo C et al..  2012.  A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.. Proceedings of the National Academy of Sciences of the United States of America. 109(21):7974-81. Abstract
2005
Kaunisto, MA, Tikka PJ, Kallela M, Leal SM, Papp JC, Korhonen A, Hämäläinen E, Harno H, Havanka H, Nissilä M et al..  2005.  Chromosome 19p13 loci in Finnish migraine with aura families.. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics. 132B(1):85-9. Abstract
2002