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机译:由雄激素受体的P.Q65x新突变引起的全形式雄激素不敏感综合征:临床表现,成像结果和分子遗传学
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Southern Med Univ Nanfang Hosp Dept Gastroenterol Guangdong Prov Key Lab Gastroenterol 1838;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Guangdong Women &
Children Hosp Children Inherited Metab &
Endocrine Dept 521 XingNan Rd;
Androgen insensitivity; Androgen receptor; Novel mutation;
机译:由雄激素受体的P.Q65x新突变引起的全形式雄激素不敏感综合征:临床表现,成像结果和分子遗传学
机译:雄激素受体基因中的L712V突变由于雄激素功能严重丧失而导致完全的雄激素不敏感综合征
机译:新型雄激素受体突变对雄激素细节综合征临床表现的功能影响
机译:雄激素细胞内细胞的临床和分子方面
机译:雄激素受体基因中一个深的内含子假性外显子激活突变引起的完全雄激素不敏感综合征
机译:患有突变C.2495G> T p。(Arc832Leu)在雄激素受体基因的外显子7中的完全雄激素不敏感综合征和传播/载体的延迟诊断:遗传,临床和伦理方面