Sort   by:  
 Page size 
UnknownDisseminated Ureaplasma infection as a cause of fatal hyperammonemia in humans.
Not available
S-EPMC4677674 | biostudies-literature
UnknownDissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors.
Not available
S-EPMC8851871 | biostudies-literature
UnknownEvaluating the Clinical Utility of Genomic Sequencing After Perinatal Death.
Not available
S-EPMC12674983 | biostudies-literature
UnknownBiallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder.
Not available
S-EPMC7447524 | biostudies-literature
UnknownComparison of causes of stillbirth and child deaths as determined by verbal autopsy and minimally invasive tissue sampling.
Not available
S-EPMC11285936 | biostudies-literature
UnknownSPTSSA variants alter sphingolipid synthesis and cause a complex hereditary spastic paraplegia.
Not available
S-EPMC10319774 | biostudies-literature
UnknownAn ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy.
Not available
S-EPMC8263055 | biostudies-literature
UnknownAdvancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network.
Not available
S-EPMC11698638 | biostudies-literature
UnknownContinuing a search for a diagnosis: the impact of adolescence and family dynamics.
Not available
S-EPMC9830697 | biostudies-literature
UnknownProgressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum.
Not available
S-EPMC8222855 | biostudies-literature
Sort   by:  
 Page size