Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation

Mather Michael W.; Hayhurst Hannah; Bacon Chris M.; Cole Theresa S.; Pan-Hammarstrom Qiang; Misbah Siraj; Gennery Andrew R.

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Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation

机译：伴肉芽肿性淋巴增生的22q11缺失综合征患儿的TNFRSF13B突变

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《The Journal of Allergy and Clinical Immunology》 |2015年第2期|共3页
作者
Mather Michael W.; Hayhurst Hannah; Bacon Chris M.; Cole Theresa S.; Pan-Hammarstrom Qiang; Misbah Siraj; Gennery Andrew R.;
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正文语种 eng
中图分类医学免疫学;
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1. Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation [J] . Mather Michael W., Hayhurst Hannah, Bacon Chris M., The Journal of Allergy and Clinical Immunology . 2015,第2期

机译：伴肉芽肿性淋巴增生的22q11缺失综合征患儿的TNFRSF13B突变
2. GRANULOMATOUS DISEASE IN TWO PATIENTS WITH 22q11 DELETION SYNDROME [J] . Sifers Travis M., Raje Nikita, Nanda Maya Journal of Clinical Immunology . 2016,第3期

机译：患有22q11综合征的两名患者的肉芽肿性疾病
3. Isolation of right internal carotid artery, persistent proatlantal 1 artery and rete mirabile in a child with 22q11 deletion syndrome [J] . Requejo Flavio, Romina Strawich Florencia, Mariela Mouratian Diana, Child's nervous system: ChNS : official journal of the International Society for Pediatric Neurosurgery . 2018,第12期

机译：右内部颈动脉的分离，持续的临床1动脉，并在22Q11删除综合征中留在儿童中的含米拉米
4. Scoliosis in the 22q11 Deletion Syndrome [C] . D. Colo, С Van Weelden, M. Rruyt, International Research Society of Spinal Deformities . 2012

机译：22Q11删除综合征中的脊柱侧凸
5. Assessment of parent/caregivers' level of guilt, worry, and uncertainty related to their child's increased risk of psychiatric disorders associated with 22q11 deletion syndrome. [D] . Hilber, Renee Elizabeth. 2009

机译：评估父母/监护人的内感，忧虑和不确定性，与他们的孩子与22q11缺失综合征相关的精神疾病风险增加有关。
6. Pulmonary Extranodal Marginal Zone Lymphoma of Mucosa-Associated Lymphoid Tissue Associated with Granulomatous Inflammation in a Child with Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome) [O] . Tawatchai Pongpruttipan, James R. Cook, Miguel Reyes-Mugica, -1

机译：黏膜相关淋巴组织相关与肉芽肿性炎症的肺结外边缘区淋巴瘤与染色体22q11.2缺失综合征患儿（DiGeorge氏综合征）
7. Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1] [O] . Wadey, R, Mckie, J, Papapetrou, C, 1999

机译：在22q11号染色体内没有缺失的大多数DiGeorge综合征/心动过速综合征的病例中，UFD1L的突变并不负责[1]

Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation

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