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    Results: 3

    1.

    Screening for nuclear genetic defects in the ATP synthase-associated genes TMEM70, ATP12 and ATP5E in patients with 3-methylglutaconic aciduria.

    Tort F, Del Toro M, Lissens W, Montoya J, Fernàndez-Burriel M, Font A, Buján N, Navarro-Sastre A, López-Gallardo E, Arranz JA, Riudor E, Briones P, Ribes A.

    Clin Genet. 2011 Sep;80(3):297-300. doi: 10.1111/j.1399-0004.2011.01650.x. No abstract available.

    PMID:
    21815885
    [PubMed - indexed for MEDLINE]
    2.

    PRRX1 is mutated in a fetus with agnathia-otocephaly.

    Sergi C, Kamnasaran D.

    Clin Genet. 2011 Mar;79(3):293-5. doi: 10.1111/j.1399-0004.2010.01531.x. No abstract available.

    PMID:
    21294718
    [PubMed - indexed for MEDLINE]
    3.

    The utility of quantitative methylation assays at imprinted genes for the diagnosis of fetal and placental disorders.

    Bourque DK, Peñaherrera MS, Yuen RK, Van Allen MI, McFadden DE, Robinson WP.

    Clin Genet. 2011 Feb;79(2):169-75. doi: 10.1111/j.1399-0004.2010.01443.x.

    PMID:
    20507345
    [PubMed - indexed for MEDLINE]

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