Clinical and Molecular Delineation of a Novel De Novo 4q28.3-31.21 Interstitial Deletion in a Patient with Developmental Delay

Rim John Hoon; Kim Seong Woo; Han Sung-Hee; Yoo Jongha

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Clinical and Molecular Delineation of a Novel De Novo 4q28.3-31.21 Interstitial Deletion in a Patient with Developmental Delay

机译：新型De Novo 4q28.3-31.21间质删除在发育迟缓患者中的临床和分子描述

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《Yonsei Medical Journal》 |2015年第6期|共3页
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Rim John Hoon; Kim Seong Woo; Han Sung-Hee; Yoo Jongha;
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1. A de novo 6p interstitial deletion and a complex translocation involving chromosomes 2, 6, and 14 in a mildly developmentally delayed patient. [J] . Misceo D, Bjorgo K, Ormerod E, American journal of medical genetics, Part A . 2008,第24期

机译：轻度发育迟缓患者的从头6p间隙缺失和涉及染色体2、6和14的复杂易位。
2. Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies. [J] . Petek E, Windpassinger C, Simma B, Journal of human genetics . 2003,第6期

机译：具有发育延迟和先天性异常的男孩的3p染色体15 Mb体质从头组织间缺失的分子表征。
3. A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial features [J] . MiyaK., ShimojimaK., SugawaraM., Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function . 2012,第1期

机译：从新发现的间质性缺失8p11.2，包括在患有红细胞增多症，精神运动发育迟缓和独特面部特征的患者中发现的ANK1
4. Clinical Implementation of DeepVoxNet for Auto-Delineation of Organs at Risk in Head and Neck Cancer Patients in Radiotherapy [C] . Siri Willems, Wouter Crijns, Agustina La Greca Saint-Esteven, International conference on medical imaging computing and computer-assisted intervention;International workshop on OR 2.0 context-aware operating theaters;International workshop on integrating medical imaging and non-imaging modalities;International workshop on clinical image-based procedures;International workshop on skin image analysis . 2018

机译：DeepVoxNet用于自动确定头颈癌患者放疗中有风险器官的临床实施
5. Evaluation of epidemiological and clinical factors in survival of patients with de novo myelodysplastic syndrome at the University of Texas MD Anderson cancer center. [D] . Sunder, Suraj. 2009

机译：德克萨斯大学MD安德森癌症中心评估从头骨髓增生异常综合症患者生存的流行病学和临床因素。
6. Clinical and Molecular Delineation of a Novel De Novo 4q28.3-31.21 Interstitial Deletion in a Patient with Developmental Delay [O] . John Hoon Rim, Seong Woo Kim, Sung-Hee Han, 2015

机译：新型De Novo 4q28.3-31.21间质缺失在发育迟缓患者中的临床和分子描述
7. Molecular characterisation of a 15 Mb constitutional de novo interstitial deletion of chromosome 3p in a boy with developmental delay and congenital anomalies [O] . Erwin Petek, Christian Windpassinger, Burkhard Simma, 2003

机译：作者：邹德勋

Clinical and Molecular Delineation of a Novel De Novo 4q28.3-31.21 Interstitial Deletion in a Patient with Developmental Delay

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