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Abrogation of MAP4K4 protein function causes congenital anomalies in humans and zebrafish.
Sci Adv. 2023 Apr 28;9(17):eade0631. doi: 10.1126/sciadv.ade0631. Epub 2023 Apr 26.
Sci Adv. 2023.
PMID: 37126546
Free PMC article.
Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3.
Nair D, Li D, Erdogan H, Yoon A, Harr MH, Bergant G, Peterlin B, Škrjanec Pušenjak M, Jayakar P, Pfundt R, Jansen S, McWalter K, Sidhu A, Saliganan S, Agolini E, Jacob A, Pasquier J, Arash R, Kahrizi K, Najmabadi H, Ropers HH, Bhoj EJ.
Nair D, et al. Among authors: saliganan s.
HGG Adv. 2021 Jan 21;2(2):100024. doi: 10.1016/j.xhgg.2021.100024. eCollection 2021 Apr 8.
HGG Adv. 2021.
PMID: 35047834
Free PMC article.
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Mutations in ARID2 are associated with intellectual disabilities.
Shang L, Cho MT, Retterer K, Folk L, Humberson J, Rohena L, Sidhu A, Saliganan S, Iglesias A, Vitazka P, Juusola J, O'Donnell-Luria AH, Shen Y, Chung WK.
Shang L, et al. Among authors: saliganan s.
Neurogenetics. 2015 Oct;16(4):307-14. doi: 10.1007/s10048-015-0454-0. Epub 2015 Aug 4.
Neurogenetics. 2015.
PMID: 26238514
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Erratum: Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3.
Nair D, Li D, Erdogan H, Yoon A, Harr MH, Bergant G, Peterlin B, Pušenjak MŠ, Jayakar P, Pfundt R, Jansen S, McWalter K, Sidhu A, Saliganan S, Agolini E, Jacob A, Pasquier J, Arash R, Kahrizi K, Najmabadi H, Ropers HH, Bhoj EJ.
Nair D, et al. Among authors: saliganan s.
HGG Adv. 2022 Jul 12;3(4):100122. doi: 10.1016/j.xhgg.2022.100122. eCollection 2022 Oct 13.
HGG Adv. 2022.
PMID: 35860725
Free PMC article.
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A patient with constitutional ring 1 chromosome characterized by SNP array CGH.
Saliganan S, Lee J, Wei S.
Saliganan S, et al.
Clin Case Rep. 2016 Mar 21;4(4):442-8. doi: 10.1002/ccr3.522. eCollection 2016 Apr.
Clin Case Rep. 2016.
PMID: 27099748
Free PMC article.
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Genetic counseling in diabetes mellitus: A practice resource of the National Society of Genetic Counselors.
Maloney KA, Mizerik E, King RH, McGinnis EM, Perkowitz S, Diamonstein CJ, Schmanski AA, Saliganan S, Shipper AG, Udler MS, Guan Y, Pollin TI.
Maloney KA, et al. Among authors: saliganan s.
J Genet Couns. 2023 Aug 3. doi: 10.1002/jgc4.1744. Online ahead of print.
J Genet Couns. 2023.
PMID: 37537905
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