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Clinical Genetics|July 4, 2015

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.

Clinical Genetics|August 31, 2016

Mitochondrial epileptic encephalopathy, 3-methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutationsM A Shahrour, O Staretz-Chacham, D Dayan, et al.

Clinical Genetics|November 4, 2016

Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone-mediated tubulinopathyB Pode-Shakked, H Barash, L Ziv, et al.

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Search research articles

Showing results (51-60 of 53) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 53 results.

Clinical Genetics|July 4, 2015

SLC1A4 mutations cause a novel disorder of intellectual disability, progressive microcephaly, spasticity and thin corpus callosumG Heimer, D Marek-Yagel, E Eyal, et al.

Clinical Genetics|August 31, 2016

Mitochondrial epileptic encephalopathy, 3-methylglutaconic aciduria and variable complex V deficiency associated with TIMM50 mutationsM A Shahrour, O Staretz-Chacham, D Dayan, et al.

Clinical Genetics|November 4, 2016

Microcephaly, intractable seizures and developmental delay caused by biallelic variants in TBCD: further delineation of a new chaperone-mediated tubulinopathyB Pode-Shakked, H Barash, L Ziv, et al.

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