| 标题 |
Follow-up of a 9-month-old boy with a prenatal history of a 17q12 microdeletion at amniocentesis encompassing HNF1B and LHX1 and no obviously phenotypic abnormality |
| 网址 | |
| DOI | |
| 其它 |
期刊:Taiwanese Journal of Obstetrics and Gynecology 作者:Chih-Ping Chen 出版日期:2026 |
| 求助人 | |
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(2025-6-4)