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UnknownChildren with Rare Nager Syndrome-Literature Review, Clinical and Physiotherapeutic Management.
Not available
S-EPMC10815867 | biostudies-literature
UnknownHaploinsufficiency of SF3B4, a component of the pre-mRNA spliceosomal complex, causes Nager syndrome.
Not available
S-EPMC3376638 | biostudies-literature
UnknownA synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndrome.
Not available
S-EPMC5315512 | biostudies-literature
UnknownSecond-trimester prenatal diagnosis of Nager syndrome with a deletion including SF3B4 detected by chromosomal microarray.
Not available
S-EPMC7069884 | biostudies-literature
UnknownA 22-Week-Old Fetus with Nager Syndrome and Congenital Diaphragmatic Hernia due to a Novel SF3B4 Mutation.
Not available
S-EPMC4188155 | biostudies-literature
UnknownAbnormal Hearing Phenotypes in "Ignorome" Knockout Mice as Predictors of Cognitive Dysfunction.
Not available
S-EPMC12933407 | biostudies-literature
UnknownDeletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.
Not available
S-EPMC11980789 | biostudies-literature
Unknown<i>Sf3b4</i> mutation in <i>Xenopus tropicalis</i> causes RNA splicing defects followed by massive gene dysregulation that disrupt cranial neural crest development.
Not available
S-EPMC10862923 | biostudies-literature
UnknownUse of Audiobooks as an Environmental Distractor to Decrease State Anxiety in Children Waiting in the Pediatric Emergency Department: A Pilot and Feasibility Study.
Not available
S-EPMC7874121 | biostudies-literature
UnknownGlycine dimerization motif in the N-terminal transmembrane domain of the high density lipoprotein receptor SR-BI required for normal receptor oligomerization and lipid transport.
Not available
S-EPMC3099662 | biostudies-literature
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