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The ethics of conducting molecular autopsies in cases of sudden death in the young.
McGuire AL, Moore Q, Majumder M, Walkiewicz M, Eng CM, Belmont JW, Nassef S, Darilek S, Rutherford K, Pereira S, Scherer SE, Sutton VR, Wolf D, Gibbs RA, Kahn R, Sanchez LA; Molecular Autopsy Consortium of Houston (MATCH). McGuire AL, et al. Among authors: nassef s. Genome Res. 2016 Sep;26(9):1165-9. doi: 10.1101/gr.192401.115. Epub 2016 Jul 13. Genome Res. 2016. PMID: 27412853 Free PMC article. No abstract available.
Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Normand EA, Braxton A, Nassef S, Ward PA, Vetrini F, He W, Patel V, Qu C, Westerfield LE, Stover S, Dharmadhikari AV, Muzny DM, Gibbs RA, Dai H, Meng L, Wang X, Xiao R, Liu P, Bi W, Xia F, Walkiewicz M, Van den Veyver IB, Eng CM, Yang Y. Normand EA, et al. Among authors: nassef s. Genome Med. 2018 Sep 28;10(1):74. doi: 10.1186/s13073-018-0582-x. Genome Med. 2018. PMID: 30266093 Free PMC article.
Spiritual Exploration in the Prenatal Genetic Counseling Session.
Sagaser KG, Shahrukh Hashmi S, Carter RD, Lemons J, Mendez-Figueroa H, Nassef S, Peery B, Singletary CN. Sagaser KG, et al. Among authors: nassef s. J Genet Couns. 2016 Oct;25(5):923-35. doi: 10.1007/s10897-015-9920-y. Epub 2016 Jan 15. J Genet Couns. 2016. PMID: 26768895
The Glu86 Residue in TBX4 Proves Critical for Human Lung Development.
Szafranski P, Gambin T, Deutsch G, Nassef SA, Bailey MC, Kearney DL, Stankiewicz P. Szafranski P, et al. Among authors: nassef sa. Am J Med Genet A. 2024 Nov 17:e63936. doi: 10.1002/ajmg.a.63936. Online ahead of print. Am J Med Genet A. 2024. PMID: 39552269
21 results