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Wiley, Human Mutation: Variation, Informatics and Disease, 5(41), p. 926-933, 2020

DOI: 10.1002/humu.23998

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Exome sequencing identifies the first genetic determinants of sirenomelia in humans

Journal article published in 2020 by François Lecoquierre ORCID, C. van Ravenswaaij-Arts, Anne‐Claire C. Brehin, Sophie Coutant, Juliette Coursimault, Anne Bazin, Wilfrid Finck, Guillaume Benoist, Marianne Begorre, Claire Beneteau ORCID, Daniel Cailliez, Pierre Chenal, Mirjam De Jong, S. Degr?, Sophie Degré and other authors.
This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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