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K J Low

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American Journal of Medical Genetics. Part A|December 10, 2025
Gene-Specific Growth Charts for ASXL3-Related DisorderE Woods, K J Low, T J Cole, et al.
Pediatric Pulmonology|May 7, 2014
A case of congenital central hypoventilation syndrome in a three-generation family with non-polyalanine repeat PHOX2B mutationK J Low, A R Turnbull, K R Smith, et al.
European Journal of Human Genetics : EJHG|March 8, 2018
Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancyK J Low, K Stals, R Caswell, et al.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|December 10, 2025
Gene-Specific Growth Charts for ASXL3-Related DisorderE Woods, K J Low, T J Cole, et al.
Pediatric Pulmonology|May 7, 2014
A case of congenital central hypoventilation syndrome in a three-generation family with non-polyalanine repeat PHOX2B mutationK J Low, A R Turnbull, K R Smith, et al.
European Journal of Human Genetics : EJHG|March 8, 2018
Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancyK J Low, K Stals, R Caswell, et al.
Pageof 1