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B Wilfert

Showing results (1-10 of 12) with videos related to

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Quintessenz Journal|September 1, 1989
[Breaking in the computer]B Wagner, B Wilfert
Quintessenz Journal|June 1, 1974
[The pregnant dental assistant]B Wagner, B Wilfert
Genome Medicine|November 29, 2017
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implicationsAmy B Wilfert, Arvis Sulovari, Tychele N Turner, et al.
Nature Genetics|November 8, 2016
Genome-wide significance testing of variation from single case exomesAmy B Wilfert, Katherine R Chao, Madhurima Kaushal, et al.
American Journal of Human Genetics|December 2, 2019
Sex-Based Analysis of De Novo Variants in Neurodevelopmental DisordersTychele N Turner, Amy B Wilfert, Trygve E Bakken, et al.
Genome Research|July 24, 2021
Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticityJakob M Goldmann, Juliet E Hampstead, Wendy S W Wong, et al.
Nature Genetics|July 27, 2021
Recent ultra-rare inherited variants implicate new autism candidate risk genesAmy B Wilfert, Tychele N Turner, Shwetha C Murali, et al.
Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.
Nature|July 15, 2020
Telomere-to-telomere assembly of a complete human X chromosomeKaren H Miga, Sergey Koren, Arang Rhie, et al.
Nature Communications|October 17, 2019
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disordersHui Guo, Elisa Bettella, Paul C Marcogliese, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Quintessenz Journal|September 1, 1989
[Breaking in the computer]B Wagner, B Wilfert
Quintessenz Journal|June 1, 1974
[The pregnant dental assistant]B Wagner, B Wilfert
Genome Medicine|November 29, 2017
Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implicationsAmy B Wilfert, Arvis Sulovari, Tychele N Turner, et al.
Nature Genetics|November 8, 2016
Genome-wide significance testing of variation from single case exomesAmy B Wilfert, Katherine R Chao, Madhurima Kaushal, et al.
American Journal of Human Genetics|December 2, 2019
Sex-Based Analysis of De Novo Variants in Neurodevelopmental DisordersTychele N Turner, Amy B Wilfert, Trygve E Bakken, et al.
Genome Research|July 24, 2021
Differences in the number of de novo mutations between individuals are due to small family-specific effects and stochasticityJakob M Goldmann, Juliet E Hampstead, Wendy S W Wong, et al.
Nature Genetics|July 27, 2021
Recent ultra-rare inherited variants implicate new autism candidate risk genesAmy B Wilfert, Tychele N Turner, Shwetha C Murali, et al.
Plos Genetics|April 5, 2013
Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1Alexandra M Lopes, Kenneth I Aston, Emma Thompson, et al.
Nature|July 15, 2020
Telomere-to-telomere assembly of a complete human X chromosomeKaren H Miga, Sergey Koren, Arang Rhie, et al.
Nature Communications|October 17, 2019
Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disordersHui Guo, Elisa Bettella, Paul C Marcogliese, et al.
Pageof 2