Associated Papers
Whole exome sequencing in three families segregating a pediatric case of sarcoidosis.
Calender A et al.
Bmc Medical Genomics, 2018
29510755 (PubMed )
Supplement: 12920_2018_338_MOESM6_ESM.xlsx › T1
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
28472130 (PubMed )
Supplement: pone.0176516.s002.xlsx › Feuil1
Host genetics and immune control of HIV-1 infection: fine mapping for the extended human MHC region in an African cohort.
Prentice HA et al.
Genes and Immunity, 0
24784026 (PubMed )
Supplement: NIHMS580846-supplement-1.xlsx › Table_S2
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