TATTON-BROWN-RAHMAN SYNDROME, A DISORDER OF DNA METHYLATION, IS A DIAGNOSTIC CONSIDERATION IN INDIVIDUALS WITH MARFANIOD FEATURES

OByrne James; Niederhoffer Karen; Armstrong Linlea

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TATTON-BROWN-RAHMAN SYNDROME, A DISORDER OF DNA METHYLATION, IS A DIAGNOSTIC CONSIDERATION IN INDIVIDUALS WITH MARFANIOD FEATURES

机译：Tatton-Brown-Rahman综合征是DNA甲基化的疾病，是具有Marfaniod特征的个体的诊断考虑因素

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来源
《American journal of medical genetics, Part A》 |2018年第6期|共2页
作者
OByrne James; Niederhoffer Karen; Armstrong Linlea;
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作者单位

Univ British Columbia Dept Med Genet Vancouver BC Canada;

Univ Alberta Dept Med Genet Edmonton AB Canada;

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原文格式 PDF
正文语种 eng
中图分类医学遗传学;
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1. TATTON-BROWN-RAHMAN SYNDROME, A DISORDER OF DNA METHYLATION, IS A DIAGNOSTIC CONSIDERATION IN INDIVIDUALS WITH MARFANIOD FEATURES [J] . OByrne James, Niederhoffer Karen, Armstrong Linlea American journal of medical genetics, Part A . 2018,第6期

机译：Tatton-Brown-Rahman综合征是DNA甲基化的疾病，是具有Marfaniod特征的个体的诊断考虑因素
2. DNA Methylation Possible Adjunct to Screening for Neurodevelopmental Syndromes: DNA methylation signatures were identified for several neurodevelopmental Mendelian disorders, and hold promise as a supplement to standard procedures for screening and detection of these diseases [J] . American journal of medical genetics, Part A . 2018,第4期

机译：DNA甲基化可能的介绍用于筛选神经发育综合征：DNA甲基化签发是针对几种神经发育孟德尔疾病鉴定的，并将承诺作为筛选和检测这些疾病的标准程序
3. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome [J] . A Starnawska, C S Hansen, T Spars?, Translational psychiatry. . 2017,第8期

机译：22q11.2缺失综合征个体与精神障碍相关的出生时DNA甲基化差异
4. WHICH ENDOCEINE DISORDER ARE WE DEALING WITH? PITUITARY PARS INTERMEDIA DYSFUNCTION VERSUS EQUINE METABOLIC SYNDROME: DIAGNOSTICS [C] . Nicholas Frank American College of Veterinary Internal Medicine Forum . 2010

机译：我们正在处理哪种内分泌障碍？垂体分配介质功能障碍与马代谢综合征：诊断
5. DNA methylation and constitutive heterochromatin in the ICF syndrome, FSHD syndrome, and normal human embryonic cell cultures. [D] . Tsien, Fern Fongyi. 2002

机译：ICF综合征，FSHD综合征和正常人胚胎细胞培养物中的DNA甲基化和组成型异染色质。
6. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome [O] . A Starnawska, C S Hansen, T Sparsø, 2017

机译：22q11.2缺失综合征个体与精神障碍相关的出生时DNA差异甲基化
7. Differential DNA methylation at birth associated with mental disorder in individuals with 22q11.2 deletion syndrome [O] . A Starnawska, C S Hansen, T Sparsø, 2017

机译：差异DNA甲基化与患有22 Q11.2缺失综合征的个体心理障碍相关的差异DNA甲基化

TATTON-BROWN-RAHMAN SYNDROME, A DISORDER OF DNA METHYLATION, IS A DIAGNOSTIC CONSIDERATION IN INDIVIDUALS WITH MARFANIOD FEATURES

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