青云英语翻译

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翻译结果1翻译结果2 翻译结果3翻译结果4翻译结果5

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先天性hypogonadotropic性腺功能减退的原因包括Kallmann综合征,这是最常见的原因在KAL1基因突变的特点是通过嗅觉丧失,腭裂,隐睾,先天性故障下丘脑gonadotropinreleasing激素(GnRH)的分泌。

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青少年先天性原因包括功能低下综合症,其中最常见的是由于 KAL1 基因突变和特点是嗅觉障碍、 腭裂、 隐睾症、 和下丘脑 gonadotropinreleasing (GnRH) 激素分泌的先天性失败。

翻译结果3复制译文编辑译文朗读译文返回顶部

青少年先天性原因包括功能低下综合症,其中最常见的是由于 KAL1 基因突变和特点是嗅觉障碍、 腭裂、 隐睾症、 和下丘脑 gonadotropinreleasing (GnRH) 激素分泌的先天性失败。

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先天原因的这一特点是长期月经不规则流.包括卡尔曼综合症,这是最常见的变异,因在1大韩航空和基因的特点是anosmia、裂颚,cryptorchidism」的失败和先天性hypothalamic gonadotropinreleasing激素(gnrh)分泌。

翻译结果5复制译文编辑译文朗读译文返回顶部

hypogonadotropic生殖腺官能不足的先天起因包括Kallmann综合症状,通常归结于一个变化在KAL1基因和描绘为嗅觉缺失、豁嘴、隐睾病和下丘脑gonadotropinreleasing的激素(GnRH)分泌物的先天失败。
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aCongenital causes of hypogonadotropic hypogonadism include Kallmann syndrome, which is most commonly due to a mutation in the KAL1 gene and is characterized by anosmia, cleft palate, cryptorchidism,and congenital failure of hypothalamic gonadotropinreleasing hormone (GnRH) secretion. hypogonadotropic生殖腺官能不足的先天起因包括Kallmann综合症状,通常归结于一个变化在KAL1基因和描绘为嗅觉缺失、豁嘴、隐睾病和下丘脑gonadotropinreleasing的激素(GnRH)分泌物的先天失败。 [translate]