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UnknownSocial Media Content of Idiopathic Pulmonary Fibrosis Groups and Pages on Facebook: Cross-sectional Analysis.
Not available
S-EPMC8204239 | biostudies-literature
UnknownDe novo STXBP1 Mutations in Two Patients With Developmental Delay With or Without Epileptic Seizures.
Not available
S-EPMC8739808 | biostudies-literature
UnknownSegregation analysis in Shwachman-Diamond syndrome: evidence for recessive inheritance.
Not available
S-EPMC1288206 | biostudies-literature
UnknownPsychosocial impact on mothers receiving expanded newborn screening results.
Not available
S-EPMC5891497 | biostudies-literature
UnknownFamily-centred care interventions for children with chronic conditions: A scoping review.
Not available
S-EPMC10837485 | biostudies-literature
UnknownIs YouTube a sufficient source of information on Sarcoidosis?
Not available
S-EPMC11386059 | biostudies-literature
UnknownALU transposition induces familial hypertrophic cardiomyopathy.
Not available
S-EPMC6978237 | biostudies-literature
UnknownShwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.
Not available
S-EPMC1275624 | biostudies-literature
UnknownVAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families.
Not available
S-EPMC3511983 | biostudies-literature
UnknownMetabolic Control and Frequency of Clinical Monitoring Among Canadian Children With Phenylalanine Hydroxylase Deficiency: A Retrospective Cohort Study.
Not available
S-EPMC12401562 | biostudies-literature
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