Embryonic expression of the human MID1 gene and its mutations in Opitz syndrome.
Pinson L; Augé J; Audollent S; Mattéi 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 14686244. ISBN 14686244.

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