FAP-like profile seen in brothers with heart damage-linked mutation
Par un écrivain mystérieux
Description
Full article: Abstracts of poster presentations
Frontiers Unraveling the Genetic Architecture of Hepatoblastoma
Three Newly Recognized Likely Pathogenic Gene Variants Associated
FAP-like profile seen in brothers with heart damage-linked mutation
Perspectives in Pediatric Pathology, Chapter 22. Testicular
Expert genomics panel disputes genes linked to a heart condition
Frontiers Unraveling the Genetic Architecture of Hepatoblastoma
Eye Problems Were First Symptoms of FAP for Family With Rare
Three Newly Recognized Likely Pathogenic Gene Variants Associated
High Hereditary Transthyretin-Related Amyloidosis Prevalence in
Cardiomyopathy correlates to nerve damage in p.A117S late‐onset
TTR Amyloidosis in Afro-Caribbean Woman Underpins Disease's Diversity
Full article: DISCOVERY: prevalence of transthyretin (TTR
Functional impairment of two novel mutations detected in
FAP Patients Show Blood Markers of Inflammation Before Amyloid
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