New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome.
Cox TC; Allen LR; Cox LL; Hopwood B; Goodwin B; Haan E; Suthers GK; Human Molecular Genetics, 2000, vol. 9, issue 17, p 2553, ISSN 09646906. ISBN 09646906.

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