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Thomas J Nicholas

Showing results (21-30 of 25) with videos related to

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Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Nature|April 24, 2025
Human de novo mutation rates from a four-generation pedigree referenceDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
NPJ Genomic Medicine|March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unitSabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Pageof 3

Showing results (21-30 of 25) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 25 results.
Nature|August 2, 2019
Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Nature|November 6, 2019
Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association powerAdam E Locke, Karyn Meltz Steinberg, Charleston W K Chiang, et al.
Biorxiv : the Preprint Server for Biology|August 16, 2024
A familial, telomere-to-telomere reference for human <i>de novo</i> mutation and recombination from a four-generation pedigreeDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
Nature|April 24, 2025
Human de novo mutation rates from a four-generation pedigree referenceDavid Porubsky, Harriet Dashnow, Thomas A Sasani, et al.
NPJ Genomic Medicine|March 23, 2025
The Utah NeoSeq Project: a collaborative multidisciplinary program to facilitate genomic diagnostics in the neonatal intensive care unitSabrina Malone Jenkins, Rachel N Palmquist, Barry Moore, et al.
Pageof 3