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Showing results (721-730 of 729) with videos related to

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Nature|March 10, 2001
Integration of cytogenetic landmarks into the draft sequence of the human genomeV G Cheung, N Nowak, W Jang, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
American Journal of Human Genetics|May 17, 2022
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing lossNatalia Trpchevska, Maxim B Freidin, Linda Broer, et al.
Science (New York, N.Y.)|March 26, 2026
Rapid adaptation and extinction in synchronized outdoor evolution experiments of <i>Arabidopsis</i>Xing Wu, Tatiana Bellagio, Yunru Peng, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Rapid adaptation and extinction across climates in synchronized outdoor evolution experiments of Arabidopsis thalianaXing Wu, Tatiana Bellagio, Yunru Peng, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Nature Genetics|November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomaliesClaire Redin, Harrison Brand, Ryan L Collins, et al.
Pageof 73

Showing results (721-730 of 729) with videos related to

Sort By:
Pageof 73
You have reached the last page of results.This site can display upto 729 results.
Nature|March 10, 2001
Integration of cytogenetic landmarks into the draft sequence of the human genomeV G Cheung, N Nowak, W Jang, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
American Journal of Human Genetics|May 17, 2022
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing lossNatalia Trpchevska, Maxim B Freidin, Linda Broer, et al.
Science (New York, N.Y.)|March 26, 2026
Rapid adaptation and extinction in synchronized outdoor evolution experiments of <i>Arabidopsis</i>Xing Wu, Tatiana Bellagio, Yunru Peng, et al.
Biorxiv : the Preprint Server for Biology|June 12, 2025
Rapid adaptation and extinction across climates in synchronized outdoor evolution experiments of Arabidopsis thalianaXing Wu, Tatiana Bellagio, Yunru Peng, et al.
Nature|September 11, 2009
Prepublication data sharing, Ewan Birney, Thomas J Hudson, et al.
Nature Genetics|January 10, 2017
SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndromeNatalie D Shaw, Harrison Brand, Zachary A Kupchinsky, et al.
Science (New York, N.Y.)|April 12, 2003
Human chromosome 7: DNA sequence and biologyStephen W Scherer, Joseph Cheung, Jeffrey R MacDonald, et al.
Nature Genetics|November 15, 2016
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomaliesClaire Redin, Harrison Brand, Ryan L Collins, et al.
Pageof 73