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Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome.
Eur J Hum Genet. 2024 Sep;32(9):1095-1105. doi: 10.1038/s41431-024-01667-y. Epub 2024 Jul 7.
Eur J Hum Genet. 2024.
PMID: 38972963
Whole-Genome Sequencing Reveals Individual and Cohort Level Insights into Chromosome 9p Syndromes.
Wang Y, Sams EI, Slaugh R, Crocker S, Hurtado EC, Tracy S, Hou YC, Markovic C, Valle K, Tate V, Belhassan K, Appelbaum E, Akinwe T, Tzovenos RS, Cao Y, Neilson A, Liu Y, Jensen N, Ghasemi R, Lindsay T, Manuel J, Couteranis S, Kremitzki M, Ustanik J, Antonacci T, Ng JK, Emory A, Metz L, DeLuca T, Lyons KN, Sinnwell T, Thomeczek B, Wang K, Sisneros N, Muraleedharan M, Kethireddy A, Corbo M, Gowda H, King K, Gurnett CA, Dutcher SK, Gooch C, Li YE, Mitchell MW, Peterson KA, Horani A, Rosenfeld JA, Bi W, Stankiewicz P, Chao HT, Posey J, Grochowski CM, Dardas Z, Puffenberger E, Pearson CE, Kooy F, Annear D, Innes AM, Heinz M, Head R, Fulton R, Toutain S; 9P-ARCH; Antonacci-Fulton L, Cui X, Mitra RD, Cole FS, Neidich J, Dickson PI, Milbrandt J, Turner TN.
Wang Y, et al. Among authors: couteranis s.
medRxiv [Preprint]. 2025 Mar 30:2025.03.28.25324850. doi: 10.1101/2025.03.28.25324850.
medRxiv. 2025.
PMID: 40196253
Free PMC article.
Preprint.
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