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Page 1
Multiple molecular diagnoses in the field of intellectual disability and congenital anomalies: 3.5% of all positive cases.
J Med Genet. 2023 Dec 21;61(1):36-46. doi: 10.1136/jmg-2023-109170.
J Med Genet. 2023.
PMID: 37586840
Interest of exome sequencing trio-like strategy based on pooled parental DNA for diagnosis and translational research in rare diseases.
Tran Mau-Them F, Duffourd Y, Vitobello A, Bruel AL, Denommé-Pichon AS, Nambot S, Delanne J, Moutton S, Sorlin A; Orphanomix Physician’s Group; Couturier V, Bourgeois V, Chevarin M, Poe C, Mosca-Boidron AL, Callier P, Safraou H, Faivre L, Philippe C, Thauvin-Robinet C.
Tran Mau-Them F, et al.
Mol Genet Genomic Med. 2021 Dec;9(12):e1836. doi: 10.1002/mgg3.1836. Epub 2021 Oct 30.
Mol Genet Genomic Med. 2021.
PMID: 34716697
Free PMC article.
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Increased diagnostic and new genes identification outcome using research reanalysis of singleton exome sequencing.
Bruel AL, Nambot S, Quéré V, Vitobello A, Thevenon J, Assoum M, Moutton S, Houcinat N, Lehalle D, Jean-Marçais N; Orphanomix Physician’s Group; Chevarin M, Jouan T, Poë C, Callier P, Tisserand E, Philippe C, Them FTM, Duffourd Y, Faivre L, Thauvin-Robinet C.
Bruel AL, et al.
Eur J Hum Genet. 2019 Oct;27(10):1519-1531. doi: 10.1038/s41431-019-0442-1. Epub 2019 Jun 23.
Eur J Hum Genet. 2019.
PMID: 31231135
Free PMC article.
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Variant recurrence in neurodevelopmental disorders: the use of publicly available genomic data identifies clinically relevant pathogenic missense variants.
Lecoquierre F, Duffourd Y, Vitobello A, Bruel AL, Urteaga B, Coubes C, Garret P, Nambot S, Chevarin M, Jouan T, Moutton S; Orphanomix Physician’s Group; Tran-Mau-Them F, Philippe C, Sorlin A, Faivre L, Thauvin-Robinet C.
Lecoquierre F, et al.
Genet Med. 2019 Nov;21(11):2504-2511. doi: 10.1038/s41436-019-0518-x. Epub 2019 Apr 30.
Genet Med. 2019.
PMID: 31036916
Free article.
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