P
Pei Chen Wu
Researcher at Mackay Memorial Hospital
Publications - 52
Citations - 495
Pei Chen Wu is an academic researcher from Mackay Memorial Hospital. The author has contributed to research in topics: Prenatal diagnosis & Amniocentesis. The author has an hindex of 13, co-authored 51 publications receiving 455 citations. Previous affiliations of Pei Chen Wu include National Taiwan University & Tatung University.
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Journal ArticleDOI
Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses
Chih-Ping Chen,Hsien Ming Lin,Yi Ning Su,Schu Rern Chern,Fuu Jen Tsai,Pei Chen Wu,Chen Chi Lee,Yu-Ting Chen,Meng Shan Lee,Chen Wen Pan,Wayseen Wang,Wayseen Wang +11 more
TL;DR: Mosaic trisomy 9 carries a high risk of fetal abnormalities warranting detailed sonographic investigation of congenital malformations and postnatal cytogenetic and polymorphic DNA marker analyses of the fetal and extraembryonic tissues confirmed the prenatal diagnosis.
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A de novo 7.9 Mb deletion in 22q13.2→qter in a boy with autistic features, epilepsy, developmental delay, atopic dermatitis and abnormal immunological findings.
Chih-Ping Chen,Shuan-Pei Lin,Schu Rern Chern,Fuu Jen Tsai,Pei Chen Wu,Chen Chi Lee,Yu-Ting Chen,Wen Ling Chen,Wayseen Wang,Wayseen Wang +9 more
TL;DR: Evidence is provided that 22q13 deletion syndrome may be associated with immune system dysfunction in addition to neuropsychiatric disorders and is associated with T-cell immune response.
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Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2-->q24.3 in a girl with autistic features and developmental delay.
Chih-Ping Chen,Shuan-Pei Lin,Schu Rern Chern,Yann Jang Chen,Fuu Jen Tsai,Pei Chen Wu,Wayseen Wang,Wayseen Wang +7 more
TL;DR: A 3 years and 4 months old girl with autistic features, developmental delay, mental retardation, language impairment and dysmorphic features, carrying a 2.8 Mb de novo deletion of chromosome 2q24.2-->q 24.3 detected by array-CGH is reported.
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Unbalanced reciprocal translocations at amniocentesis.
Chih-Ping Chen,Pei Chen Wu,Chen-Ju Lin,Schu Rern Chern,Fuu Jen Tsai,Chen Chi Lee,Dai Dyi Town,Wen Lin Chen,Li Feng Chen,Meng Shan Lee,Chen Wen Pan,Wayseen Wang,Wayseen Wang +12 more
TL;DR: Prenatal diagnosis of an unbalanced translocation may incidentally detect a balanced translocation in the family and alert structural chromosome rearrangements and prompt cytogenetic analysis of the fetus and parents if necessary.
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Short rib-polydactyly syndrome type II (Majewski): Prenatal diagnosis, perinatal imaging findings and molecular analysis of the NEK1 gene
Chih-Ping Chen,Tung Yao Chang,Chen-Yu Chen,Tao Yeuan Wang,Tao Yeuan Wang,Fuu Jen Tsai,Pei Chen Wu,Schu Rern Chern,Wayseen Wang,Wayseen Wang +9 more
TL;DR: Tibial aplasia, choroid plexus cysts and polycystic kidneys can be prominent prenatal ultrasound findings of type II SRPS and the present case provides evidence for a correlation of NEK1 mutation with type IISRPS.