Associated Papers
Rare variants found in multiplex families with orofacial clefts: Does expanding the phenotype make a difference?
Perez KKD et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
36798250 (PubMed )
Supplement: media-1.xlsx › SuppTable2_VariantsOfInterest
Exome sequencing in families with chronic central serous chorioretinopathy.
Schellevis RL et al.
Molecular Genetics & Genomic Medicine, 2019
30724488 (PubMed )
Supplement: MGG3-7-na-s005.xlsx › Family_2
Identification of potential genetic risk factors for bipolar disorder by whole-exome sequencing.
Husson T et al.
Translational Psychiatry, 2018
30518751 (PubMed )
Supplement: 41398_2018_291_MOESM1_ESM.pdf
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