Associated Papers
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants.
Tuncay IO et al.
Npj Genomic Medicine, 2022
35190550 (PubMed )
Supplement: 41525_2022_284_MOESM2_ESM.xlsx › Supplementary_Table_9
De Novo PORCN and ZIC2 Mutations in a Highly Consanguineous Family.
Castilla-Vallmanya L et al.
International Journal of Molecular Sciences, 2021
33557041 (PubMed )
Supplement: ijms-22-01549-s001.zip › Suppl_Files › Suppl_Table1_Patient_1_Variants.xlsx › Sheet1
Identification of a novel genetic locus underlying tremor and dystonia.
Monies D et al.
Human Genomics, 2017
29110692 (PubMed )
Supplement: 40246_2017_123_MOESM2_ESM.pdf
A differential association of ALOX15 polymorphisms with bone mineral density in pre- and post-menopausal women.
Cheung CL et al.
Human Heredity, 2008
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