Results 151 to 159 of about 535 (159)

"Deficiency in ELF4, X-Linked": a Monogenic Disease Entity Resembling Behçet's Syndrome and Inflammatory Bowel Disease. [PDF]

open access: yesJ Clin Immunol
Olyha SJ   +29 more
europepmc   +1 more source

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow. [PDF]

open access: yesLife Sci Alliance
Kim AH   +19 more
europepmc   +1 more source

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