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Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families.
Eur J Hum Genet. 2011 Dec;19(12):1256-63. doi: 10.1038/ejhg.2011.133. Epub 2011 Jul 27.
Eur J Hum Genet. 2011.
PMID: 21792230
Free PMC article.
A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.
Manes G, Hebrard M, Bocquet B, Meunier I, Coustes-Chazalette D, Sénéchal A, Bolland-Augé A, Zelenika D, Hamel CP.
Manes G, et al. Among authors: coustes chazalette d.
BMC Med Genet. 2011 Apr 15;12:54. doi: 10.1186/1471-2350-12-54.
BMC Med Genet. 2011.
PMID: 21496248
Free PMC article.
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