簡適悠醫生 - 婦產科
婦產科專科醫生
重點資料
- 醫務委員會註冊已驗證
- 1 個診所地點薄扶林
- 婦產科專科醫生香港大學內外全科醫學士 · 香港婦產科學院院士 · 1999 年醫科畢業
- 保險計劃資料整理中｜查看詳情
關於醫生
簡適悠醫生是薄扶林的婦產科醫生。
學歷
地點
保險計劃
常見問題
簡適悠醫生好嗎？
簡適悠醫生是薄扶林的婦產科醫生。資歷及註冊資料來自香港醫務委員會。ok.med 不評分，也不排名。
簡適悠醫生是做什麼的？
簡適悠醫生是婦產科醫生。
簡適悠醫生在哪裡看診？
簡適悠醫生於薄扶林應診。
研究及論文
共 39 篇，顯示最近 12 篇
按論文主題篩選
主題由同一批 PubMed 論文的醫學分類整理，不代表醫生提供相關診治服務。
- Prenatal Phenotype in a Neonate with Prader-Willi Syndrome and Literature Review.Diagnostics (Basel, Switzerland) · 2025
- Clinical and molecular characteristics of hemophilia A affected individuals and carriers: A 24 years experience from three centers.American journal of medical genetics. Part A · 2024
- Adrenomedullin has a pivotal role in trophoblast differentiation: A promising nanotechnology-based therapeutic target for early-onset preeclampsia.Science advances · 2023
- Prenatal diagnosis of Myhre syndrome with a heterozygous pathogenic variant in SMAD4 gene presented with thick nuchal translucency and cardiac abnormalities.Prenatal diagnosis · 2023
- Biallelic TMEM260 variants cause truncus arteriosus, with or without renal defects.Clinical genetics · 2022
- Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.NPJ genomic medicine · 2022
- Diagnostic potential of the amniotic fluid cells transcriptome in deciphering mendelian disease: a proof-of-concept.NPJ genomic medicine · 2022
- Application of Prenatal Whole Exome Sequencing for Structural Congenital Anomalies-Experience from a Local Prenatal Diagnostic Laboratory.Healthcare (Basel, Switzerland) · 2022
- Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.Genes · 2022
- Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome-An unexpected diagnosis of androgenetic chimera and its clinical implications.American journal of medical genetics. Part A · 2022
- Prenatal and postnatal diagnosis of Schuurs-Hoeijmakers syndrome: Case series and review of the literature.American journal of medical genetics. Part A · 2021
- First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing.Genes · 2021
論文資料來自 PubMed／Europe PMC，按姓名及機構自動配對；每項均可按連結核對。
僅供參考，不構成醫療建議。 閱讀完整免責聲明