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Further insight into the phenotype associated with a mutation in the ORC6 gene,causing Meier–Gorlin syndrome 3 |
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| Authors: | Stavit Allon Shalev Morad Khayat Daniel‐Spiegl Etty Orly Elpeleg |
| Affiliation: | 1. Genetics Institute, Ha'Emek Medical center, Afula, Israel;2. Rappaport Faculty of Medicine, Technion – Israel Institute of Technology, Haifa, Israel;3. Department of Obstetrics and Gynecology, Ha'emek Medical Center, Afula, Israel;4. The Monique and Jacques Roboh Department of Genetic Research, Hadassah – Hebrew University Medical Center, Jerusalem, Israel |
| Abstract: | |
| Keywords: | Meier– Gorlin syndrome exome sequencing phenotype– genotype correlation |