Associated Papers
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 762.297
Fine mapping the number of corpora lutea quantitative trait loci on SSC3: analysis of the porcine follicle-stimulating hormone receptor gene.
Sato S et al.
Animal Science Journal = Nihon Chikusan Gakkaiho, 2011
Absence of motilin gene mutations in infantile hypertrophic pyloric stenosis.
Svenningsson A et al.
Journal of Pediatric Surgery, 2008
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