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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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S Akaboshi

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Clinical Genetics|June 12, 2018

Bilateral cerebellar cysts and cerebral white matter lesions with cortical dysgenesis: Expanding the phenotype of LAMB1 gene mutationsT Okazaki, Y Saito, T Hayashida, et al.

Epilepsia|February 1, 1997

Epilepsy in peroxisomal diseasesY Takahashi, Y Suzuki, K Kumazaki, et al.

Molecular Genetics and Metabolism|March 13, 2001

Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analysesB M Hogema, S Akaboshi, M Taylor, et al.

Human Genetics|September 10, 1999

NPC1 gene mutations in Japanese patients with Niemann-Pick disease type CT Yamamoto, E Nanba, H Ninomiya, et al.

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Search research articles

Showing results (61-70 of 64) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 64 results.

Clinical Genetics|June 12, 2018

Bilateral cerebellar cysts and cerebral white matter lesions with cortical dysgenesis: Expanding the phenotype of LAMB1 gene mutationsT Okazaki, Y Saito, T Hayashida, et al.

Epilepsia|February 1, 1997

Epilepsy in peroxisomal diseasesY Takahashi, Y Suzuki, K Kumazaki, et al.

Molecular Genetics and Metabolism|March 13, 2001

Prenatal diagnosis of succinic semialdehyde dehydrogenase deficiency: increased accuracy employing DNA, enzyme, and metabolite analysesB M Hogema, S Akaboshi, M Taylor, et al.

Human Genetics|September 10, 1999

NPC1 gene mutations in Japanese patients with Niemann-Pick disease type CT Yamamoto, E Nanba, H Ninomiya, et al.

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