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Nathan R Wilson

Showing results (11-20 of 14) with videos related to

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Blood|October 3, 2013
Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemiaMajed J Dasouki, Syed K Rafi, Adam J Olm-Shipman, et al.
Scientific Reports|January 21, 2016
SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delaminationNathan R Wilson, Adam J Olm-Shipman, Diana S Acevedo, et al.
Journal of Medical Genetics|November 22, 2014
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndromePaul Kruszka, Dong Li, Margaret H Harr, et al.
Human Molecular Genetics|January 17, 2020
SPECC1L regulates palate development downstream of IRF6Everett G Hall, Luke W Wenger, Nathan R Wilson, et al.
Pageof 2

Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Blood|October 3, 2013
Exome sequencing reveals a thrombopoietin ligand mutation in a Micronesian family with autosomal recessive aplastic anemiaMajed J Dasouki, Syed K Rafi, Adam J Olm-Shipman, et al.
Scientific Reports|January 21, 2016
SPECC1L deficiency results in increased adherens junction stability and reduced cranial neural crest cell delaminationNathan R Wilson, Adam J Olm-Shipman, Diana S Acevedo, et al.
Journal of Medical Genetics|November 22, 2014
Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndromePaul Kruszka, Dong Li, Margaret H Harr, et al.
Human Molecular Genetics|January 17, 2020
SPECC1L regulates palate development downstream of IRF6Everett G Hall, Luke W Wenger, Nathan R Wilson, et al.
Pageof 2