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Orphanet Journal of Rare Diseases
|
April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
Sarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 21, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
Mubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Lot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Nature Medicine
|
June 19, 2025
Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
Steven Laurie, Wouter Steyaert, Elke de Boer, et al.
The Journal of Experimental Medicine
|
March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Mehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Nature Medicine
|
January 17, 2025
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
Steven Laurie, Wouter Steyaert, Elke de Boer, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Nature Genetics
|
January 9, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Page
of 25
Search research articles
Search
Showing results (241-250 of 249) with videos related to
Sort By:
Page
of 25
You have reached the last page of results.
This site can display upto 249 results.
Orphanet Journal of Rare Diseases
|
April 30, 2013
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP
Sarah M Nikkel, Andrew Dauber, Sonja de Munnik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 21, 2020
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
Mubeen Khan, Stéphanie S Cornelis, Marta Del Pozo-Valero, et al.
American Journal of Human Genetics
|
August 4, 2015
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Lot Snijders Blok, Erik Madsen, Jane Juusola, et al.
Nature Medicine
|
June 19, 2025
Publisher Correction: Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
Steven Laurie, Wouter Steyaert, Elke de Boer, et al.
The Journal of Experimental Medicine
|
March 8, 2023
Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease
Mehul Sharma, Daniel Leung, Mana Momenilandi, et al.
Nature Medicine
|
January 17, 2025
Genomic reanalysis of a pan-European rare-disease resource yields new diagnoses
Steven Laurie, Wouter Steyaert, Elke de Boer, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 20, 2025
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
Genome Biology
|
March 27, 2014
An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge
Catherine A Brownstein, Alan H Beggs, Nils Homer, et al.
Nature Genetics
|
January 9, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa
Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova, et al.
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of 25