Lv3
320 积分 2025-01-26 加入
Down Syndrome
2个月前
已完结
A rare occurrence of haemophilia A in a female due to compound heterozygosity of a de novo missense variant (presenting as pseudohomozygous) in F8 gene with Xq28 deletion inherited from mother
2个月前
已完结
A de novo int22h-1/int22h-2-flanked Xq28 deletion-associated preferential X-inactivation in a female with severe hemophilia B
2个月前
已完结
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