Published in
Elsevier, European Journal of Medical Genetics, 4(63), p. 103805, 2020
DOI: 10.1016/j.ejmg.2019.103805
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Split hand/foot malformation associated with 20p12.1 deletion: A case report
Journal article published in 2020 by
Lyse Ruaud,
Ricarda Flöttmann,
Malte Spielmann,
Fabienne Escande,
Lionel Van Maldergem,
Stefan Mundlos,
Juliette Piard 
This paper was not found in any repository, but could be made available legally by the author.
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