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Implementation of fetal clinical exome sequencing: Comparing prospective and retrospective cohorts.
Genet Med. 2022 Feb;24(2):344-363. doi: 10.1016/j.gim.2021.09.016. Epub 2021 Nov 30.
Genet Med. 2022.
PMID: 34906519
Free article.
Spontaneous resolution of nonimmune hydrops fetalis in a fetus with TP63 gene mutation and LZTR1 gene variants.
Hurni Y, Marangoni M, Garofalo G, Cassart M, Tomasi L, Vandernoot I, Smits G, Gounongbé C.
Hurni Y, et al. Among authors: gounongbe c.
Clin Case Rep. 2021 Aug 10;9(8):e04624. doi: 10.1002/ccr3.4624. eCollection 2021 Aug.
Clin Case Rep. 2021.
PMID: 34401172
Free PMC article.
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Middle interhemispheric variant of holoprosencephaly: First prenatal report of a ZIC2 missense mutation.
Gounongbé C, Marangoni M, Gouder de Beauregard V, Delaunoy M, Jissendi P, Cassart M, Désir J.
Gounongbé C, et al.
Clin Case Rep. 2020 Apr 30;8(7):1287-1292. doi: 10.1002/ccr3.2896. eCollection 2020 Jul.
Clin Case Rep. 2020.
PMID: 32695376
Free PMC article.
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Cell-free DNA analysis in maternal blood: comparing genome-wide versus targeted approach as a first-line screening test.
de Wergifosse S, Bevilacqua E, Mezela I, El Haddad S, Gounongbe C, de Marchin J, Maggi V, Conotte S, Badr DA, Fils JF, Guizani M, Jani JC.
de Wergifosse S, et al. Among authors: gounongbe c.
J Matern Fetal Neonatal Med. 2021 Nov;34(21):3552-3561. doi: 10.1080/14767058.2019.1686478. Epub 2019 Nov 13.
J Matern Fetal Neonatal Med. 2021.
PMID: 31722585
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