Associated Papers
Gene Identification for Ocular Congenital Cranial Motor Neuron Disorders Using Human Sequencing, Zebrafish Screening, and Protein Binding Microarrays.
Jurgens JA et al.
Investigative Ophthalmology & Visual Science, 2025
40162949 (PubMed )
Supplement: iovs-66-3-62_s002.xlsx › Supp_Table1
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays.
Jurgens JA et al.
Biorxiv : the Preprint Server for Biology, 2024
39314366 (PubMed )
Supplement: media-2.xlsx › Supp_Table1
Broad Phenotypes of Disorders/Differences of Sex Development in MAMLD1 Patients Through Oligogenic Disease.
Flück CE et al.
Frontiers in Genetics, 2019
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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