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Delayed myelination
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Waardenburg syndrome type 1 (WS1) can be distinguished from Waardenburg syndrome type 2 (WS2) by the presence of dystopia canthorum. About 96% of WS1 are due to PAX3 mutations, and SOX10 mutations have been reported in 15% of WS2.
4p
vidr2711
19-02-2020
15
1
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Tuyển tập các báo cáo nghiên cứu về sinh học được đăng trên tạp chí sinh học Journal of Biology đề tài: Systemic 5-fluorouracil treatment causes a syndrome of delayed myelin destruction in the central nervous system...
22p
toshiba3
07-09-2011
55
3
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