Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations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

Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations

Authors:	Mona Aglan Khalda Amr Samira Ismail Adel Ashour Ghada A. Otaify Mennat Allah I. Mehrez Eman H. A. Aboul‐Ezz Mona El‐Ruby Inas Mazen Mohamed S. Abdel‐Hamid Samia A. Temtamy

Affiliation:	1. Department of Clinical Genetics, Division of Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt;2. Centre of Excellence for Human Genetics, National Research Centre, Cairo, Egypt;3. Department of Medical Molecular Genetics, Division of Human Genetics and Genome Research, National Research Centre, Cairo, Egypt;4. Department of Orodental Genetics, Division of Human Genetics and Genome Research Division, National Research Centre, Cairo, Egypt;5. Department of Basic Oral Dental Science, Division of Oral and Dental Research, National Research Centre, Cairo, Egypt

Abstract:

Keywords:	Robinow syndrome autosomal recessive novel mutations Egyptians