Megan Layton Martinez

Title(s)Clinical Instructor of Psychiatry and the Behavioral Sciences (Clinician Educator)
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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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    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.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    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.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    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.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
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    NIH Funding Acknowledgment: Important - All publications resulting from the utilization of SC CTSI resources are required to credit the SC CTSI grant by including the NIH funding acknowledgment and must comply with the NIH Public Access Policy.

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