Nana Okamoto
Kobe, Japan
Last Updated: 09/26/2026
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Found 8 publications
Relationship between salivary inflammatory mediators and oral dryness during chemotherapy in patients with cancer: a cohort study.
Journal: Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
Published: November 22, 2025
Novel CLCN7 compound heterozygous mutations in intermediate autosomal recessive osteopetrosis.
Journal: Human genome variation
Published: June 05, 2017
A case with concurrent duplication, triplication, and uniparental isodisomy at 1q42.12-qter supporting microhomology-mediated break-induced replication model for replicative rearrangements.
Journal: Molecular cytogenetics
Published: March 15, 2017
A 590 kb deletion caused by non-allelic homologous recombination between two LINE-1 elements in a patient with mesomelia-synostosis syndrome.
Journal: American journal of medical genetics. Part A
Published: August 14, 2016
A novel COL11A1 mutation affecting splicing in a patient with Stickler syndrome.
Journal: Human genome variation
Published: January 01, 2015
A FRMD7 variant in a Japanese family causes congenital nystagmus.
Journal: Human genome variation
Published: November 03, 2014
A novel PTCH1 mutation in a patient with Gorlin syndrome.
Journal: Human genome variation
Published: January 01, 2014
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion.
Journal: Journal of human genetics
Published: January 20, 2012
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Last Updated: 09/26/2026