PubMed Clinical Queries
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Results for Clinical Studies: Therapy/Broad
5 of 77 results sorted by: Most RecentSee all results in PubMed (77)
Noonan syndrome: rhGH treatment and PTPN11 mutation.
Mol Genet Genomic Med. 2023. PMID: 37525886 Free PMC article.
Early-Onset Pectus Excavatum Is More Likely to Be Part of a Genetic Variation.
Eur J Pediatr Surg. 2023. PMID: 37100424 Free article.
Risk of Sudden Death in Patients With RASopathy Hypertrophic Cardiomyopathy.
J Am Coll Cardiol. 2023. PMID: 36922089 Free article.
Genomic signature of Fanconi anaemia DNA repair pathway deficiency in cancer.
Nature. 2022. PMID: 36450981 Free PMC article.
Methemoglobinemia Induced by Prilocaine in a Child With Noonan Syndrome.
Anesth Prog. 2022. PMID: 36223191 Free PMC article.