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De novo TRPM3 missense variant associated with neurodevelopmental delay and manifestations of cerebral palsy.
Cold Spring Harb Mol Case Stud. 2024 Jan 10;9(4):a006293. doi: 10.1101/mcs.a006293. Print 2023 Dec.
Cold Spring Harb Mol Case Stud. 2024.
PMID: 37684057
Free PMC article.
A Genomic Approach to Delineating the Occurrence of Scoliosis in Arthrogryposis Multiplex Congenita.
Latypova X, Creadore SG, Dahan-Oliel N, Gustafson AG, Wei-Hung Hwang S, Bedard T, Shazand K, van Bosse HJP, Giampietro PF, Dieterich K.
Latypova X, et al. Among authors: gustafson ag.
Genes (Basel). 2021 Jul 8;12(7):1052. doi: 10.3390/genes12071052.
Genes (Basel). 2021.
PMID: 34356068
Free PMC article.
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The Clinical and Genotypic Spectrum of Scoliosis in Multiple Pterygium Syndrome: A Case Series on 12 Children.
Dahan-Oliel N, Dieterich K, Rauch F, Bardai G, Blondell TN, Gustafson AG, Hamdy R, Latypova X, Shazand K, Giampietro PF, van Bosse H.
Dahan-Oliel N, et al. Among authors: gustafson ag.
Genes (Basel). 2021 Aug 6;12(8):1220. doi: 10.3390/genes12081220.
Genes (Basel). 2021.
PMID: 34440395
Free PMC article.
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