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TGFBR1 Variants Can Associate with Non-Syndromic Congenital Heart Disease without Aortopathy.
Alaamery M, Albesher N, Alhabshan F, Barnett P, Salim Kabbani M, Chaikhouni F, Ilgun A, Mook ORF, Alsaif H, Christoffels VM, van Tintelen P, Wilde AAM, Houweling AC, Massadeh S, Postma AV. Alaamery M, et al. Among authors: chaikhouni f. J Cardiovasc Dev Dis. 2023 Nov 9;10(11):455. doi: 10.3390/jcdd10110455. J Cardiovasc Dev Dis. 2023. PMID: 37998513 Free PMC article.
ADAMTS19-associated heart valve defects: Novel genetic variants consolidating a recognizable cardiac phenotype.
Massadeh S, Alhashem A, van de Laar IMBH, Alhabshan F, Ordonez N, Alawbathani S, Khan S, Kabbani MS, Chaikhouni F, Sheereen A, Almohammed I, Alghamdi B, Frohn-Mulder I, Ahmad S, Beetz C, Bauer P, Wessels MW, Alaamery M, Bertoli-Avella AM. Massadeh S, et al. Among authors: chaikhouni f. Clin Genet. 2020 Jul;98(1):56-63. doi: 10.1111/cge.13760. Epub 2020 May 19. Clin Genet. 2020. PMID: 32323311