Author/Creator: Cheng, C. - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Cheng, C.

71. VP25.09: A novel compound heterozygous mutation in STIL gene identified in a Chinese family with presentation of fetal microcephaly. (15th October 2020)

Authors:: Cheng, C.; Yang, Y.; Zhu, X.; Zhang, T.; Yang, F.; Chen, F.; Chen, X.; Zhao, S.; Guo, J.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 56(2020)Supplement 1
Page Start:: 164
Record Type:: Journal Article
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72. VP32.10: Identification of a de novo mutation of ENG gene in a fetus with pulmonary arteriovenous fistula in a Chinese family. (15th October 2020)

Authors:: Cheng, C.; Zhu, X.; Zhao, S.; Chen, X.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 56(2020)Supplement 1
Page Start:: 190
Record Type:: Journal Article
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73. VP37.21: Characterisation of placental microvascular architecture by MV‐FlowTM imaging in normal and fetal growth‐restricted pregnancies. (15th October 2020)

Authors:: Chen, X.; Xia, W.; Zhao, S.; Huang, H.; Wang, W.; Qiu, J.; Chen, X.; Cheng, C.; Tian, Z.; Rychik, J.
Journal:: Ultrasound in obstetrics & gynecology
Issue:: Volume 56(2020)Supplement 1
Page Start:: 222
Record Type:: Journal Article
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74. WHOLE‐GENOME SEQUENCING REVEALS IMMUNOTHERAPEUTIC OPTIONS FOR NATURAL‐KILLER/T CELL LYMPHOMA PATIENTS. (12th June 2019)

Authors:: Lim, J.; Huang, D.; Tang, T.; Cai, Q.; Tan, D.; Laurensia, Y.; Chia, B.; Rou‐Jun, P.; Pang, W.; Cheah, D.; Ng, C.; Hong, H.; Tan, J.; Feng, L.; Chen, J.; Han, B.; Guo, Y.; Goh, Y.; Rötzschke, O.; Cheng, C.
Journal:: Hematological oncology
Issue:: Volume 37(2019)Supplement 2
Page Start:: 203
Record Type:: Journal Article
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