作者：
Louise E,Docherty [1]
;
Faisal I,Rezwan [2]
;
Rebecca L,Poole [1]
;
Claire L S,Turner [2]
;
Emma,Kivuva [1]
;
Eamonn R,Maher [2]
;
Sarah F,Smithson [3]
;
Julian P,Hamilton-Shield [3]
;
Michal,Patalan [4]
;
Maria,Gizewska [5]
;
Jaroslaw,Peregud-Pogorzelski [6]
;
Jasmin,Beygo [7]
;
Karin,Buiting [7]
;
Bernhard,Horsthemke [8]
;
Lukas,Soellner [9]
;
Matthias,Begemann [9]
;
Thomas,Eggermann [9]
;
Emma,Baple [10]
;
Sahar,Mansour [10]
;
I Karen,Temple [10]
;
Deborah J G,Mackay [11]
作者单位：
Academic Unit of Human Development and Health, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton SO16 6YD, UK.
[1]
Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury SP2 8BJ, UK.
[2]
Peninsula Clinical Genetics Service, Royal Devon and Exeter Hospital, Exeter EX1 2ED, UK.
[3]
Department of Medical Genetics, University of Cambridge, and Cambridge NIHR Biomedical Research Centre, Addenbrooke's Hospital, Cambridge CP2 0QQ, UK.
[4]
Department of Clinical Genetics, University Hospitals Bristol, Bristol BS2 8EG, UK.
[5]
School of Clinical Sciences, University of Bristol, Bristol BS2 8AE, UK.
[6]
Department of Pediatrics, Endocrinology, Diabetology, Metabolic Diseases and Cardiology, Pomeranian Medical University, 71-252, Szczecin, Poland.
[7]
Department of Paediatric Oncology, Pomeranian Medical University, 71-252 Szczecin, Poland.
[8]
Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Hufelandstr 55, 45122 Essen, Germany.
[9]
Institut für Humangenetik, University Hospital, RWTH Aachen, Pauwelsstr 30, 52074 Aachen, Germany.
[10]
Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton SO16 5YA, UK.
[11]
St George's Healthcare NHS Trust, University of London, London, SW17 0QT UK.
[12]
主题词
流产, 自然(Abortion, Spontaneous);青少年(Adolescent);成年人(Adult);孤独性障碍(Autistic Disorder);自身抗原(Autoantigens);Beckwith-Wiedemann综合征(Beckwith-Wiedemann Syndrome);计算机模拟(Computer Simulation);DNA拷贝数变异(DNA Copy Number Variations);DNA甲基化(DNA Methylation);糖尿病(Diabetes Mellitus);后成说, 遗传(Epigenesis, Genetic);女(雌)性(Female);基因组印迹(Genomic Imprinting);人类(Humans);葡萄胎(Hydatidiform Mole);婴儿, 新生, 疾病(Infant, Newborn, Diseases);不育, 女(雌)性(Infertility, Female);男(雄)性(Male);线粒体蛋白质类(Mitochondrial Proteins);母亲(Mothers);突变(Mutation);核蛋白质类(Nuclear Proteins);肥胖症(Obesity);聚合酶链反应(Polymerase Chain Reaction);妊娠(Pregnancy);序列分析, DNA(Sequence Analysis, DNA);Silver-Russell综合征(Silver-Russell Syndrome);双生, 单卵(Twins, Monozygotic);子宫肿瘤(Uterine Neoplasms);青年人(Young Adult)
DOI
10.1038/ncomms9086
PMID
26323243
发布时间
2022-03-09
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