Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
Pinson, L.; Augé, J.; Audollent, S.; Matt&eeacute;i, G.; Etchevers, H.; Gigarel, N.; Razavi, F.; Lacombe, D.; Odent, S.; Le Merrer, M.; Amiel, J.; Munnich, A.; Meroni, G.; Lyonnet, S.; Vekemans, M.; Attié-Bitach, T.; Journal of Medical Genetics, 2004, vol. 41, issue 5, p 381, ISSN 00222593. ISBN 14686244.

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