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Identification of a novel SNP mutation causing drop-out alleles in a paternity test using combined nest and touch-down PCR with Sanger sequencing
Wang, Hongbo, Shi, Botong, Guo, Liang, Zou, Yingnan, Liu, Bo, Yao, Jun, Wang, Baojie, Wang, Zhengdong, Li, Xin, Mu, Gang, Ren, Fu
Published in Annals of human biology (31.12.2024)
Published in Annals of human biology (31.12.2024)
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Molecular Screening via Sanger Sequencing of the Genetic Variants in Non-Alcoholic Fatty Liver Disease Subjects in the Saudi Population: A Hospital-Based Study
Alsaif, Faisal, Al-hamoudi, Waleed, Alotaiby, Maram, Alsadoon, Amani, Almayouf, Mohammed, Almadany, Hadeel, Abuhaimed, Jawahir, Ghufran, Noman, Merajuddin, Ahmed, Ali Khan, Imran
Published in Metabolites (01.12.2022)
Published in Metabolites (01.12.2022)
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A Genotypic Test for HIV-1 Tropism Combining Sanger Sequencing with Ultradeep Sequencing Predicts Virologic Response in Treatment-Experienced Patients
Kagan, Ron M., Johnson, Erik P., Siaw, Martin, Biswas, Pinaki, Chapman, Douglass S., Su, Zhaohui, Platt, Jamie L., Pesano, Rick L.
Published in PloS one (27.09.2012)
Published in PloS one (27.09.2012)
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Expanding the mutation spectrum in 130 probands with ARPKD: identification of 62 novel PKHD1 mutations by sanger sequencing and MLPA analysis
Melchionda, Salvatore, Palladino, Teresa, Castellana, Stefano, Giordano, Mario, Benetti, Elisa, De Bonis, Patrizia, Zelante, Leopoldo, Bisceglia, Luigi
Published in Journal of human genetics (01.09.2016)
Published in Journal of human genetics (01.09.2016)
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NPM1 Mutation Analysis in Acute Myeloid Leukemia: Comparison of Three Techniques - Sanger Sequencing, Pyrosequencing, and Real-Time Polymerase Chain Reaction
Kumar, Dushyant, Mehta, Anurag, Panigrahi, Manoj Kumar, Nath, Sukanta, Saikia, Kandarpa Kumar
Published in Turkish journal of haematology (01.03.2018)
Published in Turkish journal of haematology (01.03.2018)
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Phenotype-genotype correlation with Sanger sequencing identified retinol dehydrogenase 12 (RDH12) compound heterozygous variants in a Chinese family with Leber congenital amaurosis
Li, Yun, Pan, Qing, Gu, Yang-shun
Published in Journal of Zhejiang University. B. Science (01.05.2017)
Published in Journal of Zhejiang University. B. Science (01.05.2017)
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16S rRNA Gene PCR/Sequencing of Heart Valves for Diagnosis of Infective Endocarditis in Routine Clinical Practice
Hong, Hyo-Lim, Flurin, Laure, Greenwood-Quaintance, Kerryl E., Wolf, Matthew J., Pritt, Bobbi S., Norgan, Andrew P., Patel, Robin
Published in Journal of clinical microbiology (23.08.2023)
Published in Journal of clinical microbiology (23.08.2023)
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Distribution pattern of UGT1A6 and UGT2B7 gene polymorphism and its impact on the pharmacokinetics of valproic acid and carbamazepine: Prospective genetic association study conducted in Pakistani patients with epilepsy
Saleh Faisal, Muhammad, Jamil, Ayesha, Ali, Niaz, Alshahrani, Abdulrahman M., Almarshad, Feras
Published in Gene (20.01.2024)
Published in Gene (20.01.2024)
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Clinical and genetic investigation of 14 families with various forms of short stature syndromes
Khan, Fati Ullah, Khan, Hammal, Ullah, Kifayat, Nawaz, Shoaib, Abdullah, Khan, Muhammad Javed, Ahmed, Sohail, Ilyas, Muhammad, Ali, Amjad, Ullah, Imran, Sohail, Aamir, Hussain, Shabir, Ahmad, Farooq, Faisal, Sufyan, Raza, Hayat, Amir, Hanif, Tooba, Bibi, Fatima, Hayat, Maria, Ullah, Rehmat, Khan, Inam Ullah, Ali, Raja Hussain, Hasni, Muhammad Sharif, Ali, Hamid, Bilal, Muhammad, Peralta, Susana, Buchert, Rebecca, Zehri, Zamrud, Hassan, Gul, Liaqat, Khurrum, Zahid, Muhammad, Shah, Khadim, Mikitie, Outi, Haack, Tobias B., Ji, Weizhen, Lakhani, Saquib A., Ansar, Muhammad, Ahmad, Wasim
Published in Clinical genetics (01.09.2024)
Published in Clinical genetics (01.09.2024)
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