"
Tay-Sachs carrier screening in the genomics age: Gene sequencing versus enzyme analysis in non-Jewish individuals"
written by Charles M. Strom, Noh Jin Park, Craig Morgan, Raynah Lobo, Beryl Crossley, Rajesh Sharma, Reuben Bonilla-Guerrero, Denise Salazar,
published by
Open Journal of Genetics,
Vol.3 No.1, 2013
has been cited by the following article(s):
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[1]
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Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics
2019
DOI:10.1016/B978-0-12-812536-6.00010-9
|
|
|
|
|
[2]
|
Genotype-phenotype correlation of gangliosidosis mutations using in silico tools and homology modeling
Molecular Genetics and Metabolism Reports,
2019
DOI:10.1016/j.ymgmr.2019.100495
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|
|
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|
[3]
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Screening for Tay‐Sachs disease carriers by full‐exon sequencing with novel variant interpretation outperforms enzyme testing in a pan‐ethnic cohort
Molecular Genetics & Genomic Medicine,
2019
DOI:10.1002/mgg3.836
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|
|
|
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[4]
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Tay-Sachs Carrier Screening by Enzyme and Molecular Analyses in the New York City Minority Population
Genetic Testing and Molecular Biomarkers,
2016
DOI:10.1089/gtmb.2015.0302
|
|
|
|
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[5]
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Next-generation DNA sequencing ofHEXA: a step in the right direction for carrier screening
Molecular Genetics & Genomic Medicine,
2013
DOI:10.1002/mgg3.37
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|
|
|
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[6]
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Next‐generation DNA sequencing of HEXA: a step in the right direction for carrier screening
Molecular Genetics & Genomic Medicine,
2013
DOI:10.1002/mgg3.37
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|
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|