Associated Papers
Idiopathic hypereosinophilic syndrome: Potential pathologic somatic gene variants identified by exome sequencing.
Ferrer A et al.
The Journal of Allergy and Clinical Immunology. Global, 2025
41089458 (PubMed )
Supplement: mmc1.xlsx › Suppl_2
Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach.
Rai A et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Current gene panels account for nearly all homologous recombination repair-associated multiple-case breast cancer families.
Matis TS et al.
Npj Breast Cancer, 2021
De novo mutations in moderate or severe intellectual disability.
Hamdan FF et al.
Plos Genetics, 2014
25356899 (PubMed )
Supplement: pgen.1004772.s004.xlsx › 1635.580
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