Turner's syndrome with interstitial and presumptive terminal deletion short arm X

Sillesen; Ingelis; Rasmussen; Kirsten; Nielsen; Johannes

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Turner's syndrome with interstitial and presumptive terminal deletion short arm X

机译：特纳氏综合征伴间质性和推测性末端缺失短臂X

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来源
《Hereditas》 |1976年第1期|共3页
作者
Sillesen; Ingelis; Rasmussen; Kirsten; Nielsen; Johannes;
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中图分类遗传学;
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1. Hypertensive Cerebral Hemorrhage in a Patient with Turner Syndrome Caused by Deletion in the Short Arm of the X Chromosome [J] . Hori Yusuke S., Ohkura Takahiro, Ebisudani Yuki, Pediatric neurosurgery . 2018,第3期

机译：在X染色体短臂上缺失引起的患者患者高血压脑出血
2. Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in turner syndrome [J] . BondyC., BakalovV.K., ChengC., Journal of Medical Genetics . 2013,第10期

机译：双尖瓣主动脉瓣和主动脉缩窄与特纳综合征中X染色体短臂的缺失有关
3. A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows [J] . Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Taiwanese journal of obstetrics and gynecology . 2018,第4期

机译：一名具有18p缺失综合征的13岁女孩，表现出特纳综合征样临床特征，包括身材矮小，手蹼短，后发线低，眼睑浮肿和肘部抬高角度
4. On ordered syndromes for multi insertion/deletion error-correcting codes [C] . Manabu Hagiwara IEEE International Symposium on Information Theory . 2016

机译：关于多重插入/删除纠错码的有序校正子
5. The New Face of Genetics: Education of the Medical Community to Improve Patient Satisfaction. A Comparison of 22q11.2 Deletion Syndrome and Turner Syndrome. [D] . Moser, Cory R. 2013

机译：遗传学的新面貌：医学界对提高患者满意度的教育。 22q11.2删除综合征和特纳综合征的比较。
6. Original article: Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome [O] . Carolyn Bondy, Vladimir K Bakalov, Clara Cheng, -1

机译：原始文章：二尖瓣主动脉瓣和主动脉缩窄与特纳综合征中X染色体短臂的缺失有关
7. Bicuspid aortic valve and aortic coarctation are linked to deletion of the X chromosome short arm in Turner syndrome [O] . Carolyn Bondy, Vladimir K Bakalov, Clara Cheng, 2013

机译：双裂主动脉瓣和主动脉缩窄与卷综合征的X染色体短臂的缺失连接

Turner's syndrome with interstitial and presumptive terminal deletion short arm X

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