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Fetal phenotype of 17q12 microdeletion syndrome: renal echogenicity and congenital diaphragmatic hernia in 2 cases |
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| Authors: | Patrick Yap George McGillivray Fiona Norris Joanne M Said Louise Kornman Zornitza Stark |
| Institution: | 1. Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Melbourne, Australia
Fetal Medicine Unit, Royal Women's Hospital, Melbourne, Australia;2. Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Melbourne, Australia;3. Fetal Medicine Unit, Royal Women's Hospital, Melbourne, Australia Maternal Fetal Medicine, Sunshine Hospital, Western Health, Melbourne, Australia NorthWest Academic Centre, The University of Melbourne, Melbourne, Australia;4. Fetal Medicine Unit, Royal Women's Hospital, Melbourne, Australia;5. Victorian Clinical Genetics Services, Murdoch Childrens Research Institute, Melbourne, Australia Maternal Fetal Medicine, Sunshine Hospital, Western Health, Melbourne, Australia |
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