Megan Layton

Title(s)Clinical Instructor of Psychiatry and the Behavioral Sciences (Clinician Educator) (Part-Time)
SchoolKeck School of Medicine of Usc
Address1031 W. 34th Street
University Park Campus
Los Angeles CA 90089
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    1. Assignment of a gene (NEMI) for autosomal dominant nemaline myopathy to chromosome I. Am J Hum Genet. 1992 Mar; 50(3):576-83. Laing NG, Majda BT, Akkari PA, Layton MG, Mulley JC, Phillips H, Haan EA, White SJ, Beggs AH, Kunkel LM, et al. PMID: 1347195; PMCID: PMC1684287.
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    2. Two distinct mutations in a single dystrophin gene: chance occurrence or premutation? Am J Med Genet. 1992 Mar 01; 42(5):688-92. Laing NG, Layton MG, Johnsen RD, Chandler DC, Mears ME, Goldblatt J, Kakulas BA. PMID: 1632439.
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    3. Identification of Duchenne muscular dystrophy genomic probe P20 constant Taql fragment corresponding to the EcoRV and Mspl polymorphisms. Prenat Diagn. 1991 Jan; 11(1):63-7. Laing NG, Walker AP, Akkari PA, Chandler DC, Layton MG, Mears ME, Yamada T, Bartlett RJ, Pericak-Vance MA, Hung WY, et al. PMID: 1709287.
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    4. Duchenne muscular dystrophy (DMD) gene cDNA 8 PstI and TaqI polymorphisms involve exon 51 of the HindIII map. Nucleic Acids Res. 1990 Jul 25; 18(14):4284. Laing NG, Akkari PA, Chandler DC, Thomas HE, Layton MG, Mears ME, Kakulas BA. PMID: 1974044; PMCID: PMC331223.
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