New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome (Q28141107)
scientific article (publication date: 12 October 2000)
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(P31) (Q13442814)
(P304) 2553-62
(P407) (Q1860)
(P433) 17
(P478) 9
(P577) Thursday, October 12, 2000
(P1433) (Q2720965)
(P1476) "New mutations in MID1 provide support for loss of function as the cause of X-linked Opitz syndrome" (language: en)
(P2093) T C Cox
L R Allen
L L Cox
B Hopwood
B Goodwin
E Haan
G K Suthers
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description scientific article (publication date: 12 October 2000)

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