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Nature
|
March 23, 2018
Corrigendum: Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification
Sven Reischauer, Oliver A Stone, Alethia Villasenor, et al.
European Journal of Human Genetics : EJHG
|
August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
Adam Ameur, Johan Dahlberg, Pall Olason, et al.
Nature
|
July 15, 2016
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification
Sven Reischauer, Oliver A Stone, Alethia Villasenor, et al.
Elife
|
May 4, 2016
The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing
Alvaro Martinez Barrio, Sangeet Lamichhaney, Guangyi Fan, et al.
Genome Medicine
|
November 8, 2019
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, et al.
Human Molecular Genetics
|
August 3, 2013
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
Dagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, et al.
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Search research articles
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Showing results (51-60 of 56) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 56 results.
Nature
|
March 23, 2018
Corrigendum: Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification
Sven Reischauer, Oliver A Stone, Alethia Villasenor, et al.
European Journal of Human Genetics : EJHG
|
August 24, 2017
SweGen: a whole-genome data resource of genetic variability in a cross-section of the Swedish population
Adam Ameur, Johan Dahlberg, Pall Olason, et al.
Nature
|
July 15, 2016
Cloche is a bHLH-PAS transcription factor that drives haemato-vascular specification
Sven Reischauer, Oliver A Stone, Alethia Villasenor, et al.
Elife
|
May 4, 2016
The genetic basis for ecological adaptation of the Atlantic herring revealed by genome sequencing
Alvaro Martinez Barrio, Sangeet Lamichhaney, Guangyi Fan, et al.
Genome Medicine
|
November 8, 2019
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Anna Lindstrand, Jesper Eisfeldt, Maria Pettersson, et al.
Human Molecular Genetics
|
August 3, 2013
A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling
Dagmar Wieczorek, Nina Bögershausen, Filippo Beleggia, et al.
Page
of 6