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

翻译结果1复制译文编辑译文朗读译文返回顶部

ditions。 hypogonadotropic hypoonadisminclude Kallmann综合征mostcommonly,这是由于在KAL1基因突变的特点是嗅觉丧失,腭裂,隐睾,先天性故障,下丘脑gonadotropinreleasing激素(GnRH)的分泌的先天性原因。

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ditions。先天性的青少年 hypoonadisminclude 功能低下综合症,这是由于到 KAL1 基因突变,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的原因。

翻译结果3复制译文编辑译文朗读译文返回顶部

ditions。先天性的青少年 hypoonadisminclude 功能低下综合症,这是由于到 KAL1 基因突变,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的原因。

翻译结果4复制译文编辑译文朗读译文返回顶部

增加项目。 这一特点是长期的先天原因hypoonadisminclude卡尔曼综合症,这是由于一个mostcommonly突变基因的1大韩航空和的特点是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

ditions。 hypogonadotropic hypoonadisminclude Kallmann综合症状的先天起因, mostcommonly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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aditions. Congenital causes of hypogonadotropic hypoonadisminclude Kallmann syndrome, which is mostcommonly 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. ditions。 hypogonadotropic hypoonadisminclude Kallmann综合症状的先天起因, mostcommonly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]