Výsledky vyhledávání - "Eugene E. L. Saw"

Identification of novel microsatellite markers <1 Mb from theHBBgene and development of a single-tube pentadecaplex PCR panel of highly polymorphic markers for preimplantation genetic diagnosis of beta-thalassemia

Autor: Arnold S.C. Tan, Samuel S. Chong, Felicia S.H. Cheah, Min Chen, Eugene E. L. Saw

Publikováno v: ELECTROPHORESIS. 36:2914-2924

Beta (β)-thalassemia is one of the most common monogenic diseases worldwide. Affected pregnancies can be avoided through preimplantation genetic diagnosis (PGD), which commonly involves customized assays to detect the different combinations of β-gl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af97fe920d8f76c50d3a49901cd41bb9
https://doi.org/10.1002/elps.201500146

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Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome

Autor: Arnold S.C. Tan, Sadhana Nadarajah, Wendy Wong, Min Chen, Hai-Yang Law, Eugene E. L. Saw, Joyce Mathew, Cheryl Lim, P.C. Wong, Jerry Kok Yen Chan, Samuel S. Chong, Melinda L. H. Chan, Felicia S.H. Cheah

Publikováno v: Prenatal Diagnosis. 35:534-543

Objective To develop a single-tube multi-marker assay for improved preimplantation genetic diagnosis (PGD) of deletional and/or non-deletional Hb Bart's hydrops fetalis syndrome, providing haplotype confirmation of deletional status, and maximization

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6b832ad49d6eab9771977b82c0262828
https://doi.org/10.1002/pd.4568

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Rapid and reliable preimplantation genetic diagnosis of common hemoglobin Bart's hydrops fetalis syndrome and hemoglobin H disease determinants using an enhanced single-tube decaplex polymerase chain reaction assay

Autor: Sadhana Nadarajah, Seong Feei Loh, Su Ling Yu, Felicia S.H. Cheah, P.C. Wong, Samuel S. Chong, Ethiraj B. Prasath, Suresh Nair, Eugene E. L. Saw, Heng Hao Tan, Arnold S.C. Tan, Min Chen, Soon Chye Ng

Publikováno v: American journal of hematology. 90(9)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40a3ff971a9ed1a3765c0c27296a09b8
https://pubmed.ncbi.nlm.nih.gov/26043722

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Single-tube nonaplex microsatellite PCR panel for preimplantation genetic diagnosis of Hb Bart's hydrops fetalis syndrome

Autor: Min, Chen, Jerry K Y, Chan, Sadhana, Nadarajah, Arnold S C, Tan, Melinda L H, Chan, Joyce, Mathew, Eugene E L, Saw, Cheryl, Lim, Wendy, Wong, Felicia S H, Cheah, Hai-Yang, Law, Peng-Cheang, Wong, Samuel S, Chong

Publikováno v: Prenatal diagnosis. 35(6)

To develop a single-tube multi-marker assay for improved preimplantation genetic diagnosis (PGD) of deletional and/or non-deletional Hb Bart's hydrops fetalis syndrome, providing haplotype confirmation of deletional status, and maximization of linkag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::c0190f645f7f17d684869239d2581dcc
https://pubmed.ncbi.nlm.nih.gov/25641621

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