519 results on '"Chen, Wen-lin"'
Search Results
102. Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism
103. Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome
104. Long Term Probiotics Administration Alleviates Immunosenescence in Senescence‐accelerated Mouse Prone 8 (SAMP8)
105. Effect of Long‐Term Supplementation Lactobacillus paracasei on Body Composition in senescence‐accelerated mouse P8 (SAMP8)
106. Age‐Related Decrease of Neurotransmitters in Senescence‐Accelerated‐8 Mice
107. Researches on robot system architecture in CPS
108. Prenatal diagnosis and molecular cytogenetic characterization of a de novo3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin
109. Prenatal diagnosis and molecular cytogenetic characterization of de novodistal 5p deletion and distal 22q duplication
110. Enhancement of the impact toughness in Sn–Ag–Cu/Cu solder joints via modifying the microstructure of solder alloy
111. Mosaic tetrasomy 9p at amniocentesis: Prenatal diagnosis, molecular cytogenetic characterization, and literature review
112. Mosaic distal 9p deletion or 46,XY,del(9)(p23)/46,XY at amniocentesis in a pregnancy associated with perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome
113. Mosaic distal 10q deletion or 46,XY,del(10) (q26.13)/46,XY at amniocentesis and cordocentesis in a pregnancy associated with cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, perinatal progressive decrease of the aneuploid cell line and a favorable fetal outcome
114. Prenatal diagnosis of a distal 3p deletion associated with fetoplacental chromosomal discrepancy and confined placental mosaicism detected by array comparative genomic hybridization
115. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial duplication of 14q (14q31.3→q32.12) associated with abnormal maternal serum biochemistry
116. A facile protocol for N-alkylation of azoles using KOtBu as base under NBS-promoted conditions
117. Opposite response to hypoxia by breast cancer cells between cell proliferation and cell migration: A clue from microRNA expression profile.
118. Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise
119. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis
120. Trisomy 7 mosaicism at amniocentesis: Interphase FISH, QF-PCR, and aCGH analyses on uncultured amniocytes for rapid distinguishing of true mosaicism from pseudomosaicism
121. Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1–q21.2 and 5-Mb deletion of 21q22.3
122. Content Classification by folksonomies: Framework of Social Bookmarking System
123. Framework for Classifying Website Content Based on Folksonomy in Social Bookmarking
124. Interfacial reaction and mechanical evaluation in multi-level assembly joints with ENEPIG under bump metallization via drop and high speed impact test
125. Neuroprotective effects of hydrogen sulfide and the underlying signaling pathways
126. Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion
127. Mosaic deletion-duplication syndrome of chromosome 3: Prenatal molecular cytogenetic diagnosis using cultured and uncultured amniocytes and association with fetoplacental discrepancy
128. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
129. Prenatal diagnosis and molecular cytogenetic characterization of a de novointerchromosomal insertion of ins(1;8)(p22.1;q22q23)
130. Dynamic Recrystallization Microstructure Grain Size Prediction of 7075 Aluminum Alloy Piston Prepared by Isothermal Extrusion
131. Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry
132. Topological Optimization for Damping Structure of Cylindrical Shell Based on DIMFM
133. Finite Element Research on Damping of Viscoelastic Free Layer Damping Sheet
134. Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1and PAFAH1B1in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay
135. Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9and CDH10in a fetus with congenital heart disease on prenatal ultrasound
136. Study of elastic deformation on dimensional accuracy in ironing process of spur gear
137. Unbalanced and Balanced Acrocentric Rearrangements Involving Chromosomes Other Than Chromosome 21 at Amniocentesis
138. Effectiveness of an Education Program for Optimising Nurses’ Management of Children's Postoperative Pain
139. Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13
140. Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review
141. The Design of High Power LED Headlamp
142. ChemInform Abstract: Synthesis of Multisubstituted Imidazoles via Copper-Catalyzed [3 + 2] Cycloadditions.
143. Prenatal diagnosis and molecular cytogenetic characterization of a de novo interstitial deletion of 7q (7q22.1→q31.1)
144. A 53.6 GHz direct injection-locked frequency divider with a 72% locking range in 65 nm CMOS technology
145. ChemInform Abstract: A Facile Protocol for N-Alkylation of Azoles Using KOtBu as Base under NBS-Promoted Conditions.
146. Prenatal diagnosis of partial trisomy 3q (3q27.3→qter) and partial monosomy 14q (14q31.3→qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints
147. Synthesis of Multisubstituted Imidazoles via Copper-Catalyzed [3 + 2] Cycloadditions
148. A facile protocol for N-alkylation of azoles using KO Bu as base under NBS-promoted conditions
149. Nurses' and parents' attitudes toward pain management and parental participation in postoperative care of children
150. Microstructure Evolution of Dynamic Recrystallization of 42CrMo Steel during Multi-Stage Forging by FEM
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