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we propose that genetic factors contribu
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many cases have still not been explained. METHODS: We have identified a pericentric inversion of the X chromosome inv(X)(p22.3;q13.2) segregating in a family where two male carriers have severe MR...
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Pierre-Pascal Lenck; Aniksztejn
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10.1136/jmg.36.10.754
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Iurov IuV.;"Zh Nevrol Psikhiatr Im S S Korsakova. 2005;105(7):4-11.";Iurov IIu;Zh Nevrol Psikhiatr Im S S Korsakova;2005;25/08/2005;;;
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10.1016/s0378-1119(99)00279-6
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Nadine; Badens
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the breakpoint is approximately 134 kb from the 5' end of the androgen receptor (AR) gene. CONCLUSIONS: Genetic defects
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10.1086/302499
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