Výsledky vyhledávání - "Melinda L H, Chan"

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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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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Preimplantation genetic diagnosis of chromosome translocations by analysis of polymorphic short tandem repeats

Autor: Seong Feei, Loh, Peng Cheang, Wong, Boran, Jiang, Gare Hoon, Yeo, Arnold S C, Tan, Ethiraj Balaji, Prasath, Joyce, Mathew, Melinda L H, Chan, Wei Chin, Tan, Mahesh, Choolani, Christine H A, Yap, Samuel S, Chong

Publikováno v: Singapore medical journal. 53(10)

We aimed to develop and implement a short tandem repeat (STR) polymerase chain reaction alternative to fluorescence in situ hybridisation (FISH) for the preimplantation genetic diagnosis (PGD) of chromosomal translocations.Selected informative STRs l

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::10a017316f30629384f0ca17d21b8b7c
https://pubmed.ncbi.nlm.nih.gov/23112015

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Simplified PGD of common determinants of haemoglobin Bart's hydrops fetalis syndrome using multiplex-microsatellite PCR

Autor: Seong Feei Loh, Melinda L. H. Chan, Wei Chin Tan, Ethiraj B. Prasath, Angela Ho, Sherry S.Y. Ho, Boran Jiang, Mui Nee Lim, Arnold S. C. Tan, Joyce Mathew, Gare Hoon Yeo, Mahesh Choolani, Christine Yap, Samuel S. Chong, Peng Cheang Wong, Wen Wang

Publikováno v: Reproductive biomedicine online. 21(5)

The high incidence of double-gene deletions in α-thalassaemia increases the risk of having pregnancies with homozygous α(0)-thalassaemia, the cause of the lethal haemoglobin (Hb) Bart's hydrops fetalis syndrome. Preimplantation genetic diagnosis (P

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7dea44ffcd8cc7fed21e9fa1d3dd7ed
https://pubmed.ncbi.nlm.nih.gov/20864413

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