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Nature Genetics
|
June 3, 2000
Mutations in ABCC6 cause pseudoxanthoma elasticum
A A Bergen, A S Plomp, E J Schuurman, et al.
Atherosclerosis
|
May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosis
A A W Weterings, I A W van Rijsingen, A S Plomp, et al.
NPJ Genomic Medicine
|
November 16, 2021
Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
R Koster, R D Brandão, D Tserpelis, et al.
Journal of Intellectual Disability Research : JIDR
|
October 9, 2020
Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes
P A Mulder, I D C van Balkom, A M Landlust, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 14) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 14 results.
Nature Genetics
|
June 3, 2000
Mutations in ABCC6 cause pseudoxanthoma elasticum
A A Bergen, A S Plomp, E J Schuurman, et al.
Atherosclerosis
|
May 11, 2013
A novel lamin A/C mutation in a Dutch family with premature atherosclerosis
A A W Weterings, I A W van Rijsingen, A S Plomp, et al.
NPJ Genomic Medicine
|
November 16, 2021
Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq
R Koster, R D Brandão, D Tserpelis, et al.
Journal of Intellectual Disability Research : JIDR
|
October 9, 2020
Development, behaviour and sensory processing in Marshall-Smith syndrome and Malan syndrome: phenotype comparison in two related syndromes
P A Mulder, I D C van Balkom, A M Landlust, et al.
Page
of 2