| 篇名 | 作者 | 刊名 | 出版年 | 查看 |
|---|
| Prenatal molecular diagnosis for Apert syndrome |
Osada, H.;Ishii, J.;Sekiya, S.; |
International Journal of Gynecology & Obstetrics |
1996-11-01 |
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| Application of the three-dimensional maximum mode in prenatal diagnosisof Apert syndrome |
Esser, T.;Rogalla, P.;Bamberg, C.;Kalache, K.D.; |
American Journal of Obstetrics and Gynecology |
2005-11-01 |
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| Application of the three-dimensional maximum mode in prenatal diagnosisof Apert syndrome |
Esser, T.;Rogalla, P.;Bamberg, C.;Kalache, K.D.; |
American Journal of Obstetrics and Gynecology |
2005-11-01 |
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| Rapid detection of de novo P253R mutation in FGFR2 using unculturedamniocytes in a pregnancy affected by polyhydramnios, Blake's pouch cyst,and Apert syndrome |
Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Chen, C.Y.;Su, J.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-06-01 |
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