Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199–214 cluster in the skeletal features of the condition期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Two further patients with the 1q24 deletion syndrome expand the phenotype: A possible role for the miR199–214 cluster in the skeletal features of the condition

Authors:	Tazeen Ashraf Morag N. Collinson Joanna Fairhurst Rubin Wang Louise C. Wilson Nicola Foulds

Affiliation:	1. Guy's Clinical Genetics Service, Guy's Hospital, London, United Kingdom;2. Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, Wiltshire, United Kingdom;3. Radiology Department, University Hospital Southampton NHS Foundation Trust, Southampton, Hampshire, United Kingdom;4. North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom;5. Wessex Clinical Genetics Service, University Hospital Southampton NHS Foundation Trust, Southampton, Hampshire, United Kingdom

Abstract:

Keywords:	genetics microdeletion 1q24 dynamin‐3 DNM3 dysmorphology syndrome skeletal phenotype miR199