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 › 1164.429
Germline mutations of inhibins in early-onset ovarian epithelial tumors.
Tournier I et al.
Human Mutation, 2014
24302632 (PubMed )
Supplement: humu0035-0294-SD1.pdf
An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures.
Yalçin O et al.
Epilepsia, 2011
Expansion of the germline analysis for the INHA gene in Indian women with ovarian failure.
Dixit H et al.
Human Reproduction (oxford, England), 2006
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