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Publications by Junji Nishimoto

Preferential Paternal Origin of Microdeletions Caused by Prezygotic Chromosome or Chromatid Rearrangements in Sotos Syndrome

American Journal of Human Genetics

English

Related publications

Paternal Origin of the De Novo Deleted Chromosome 4 in Wolf-Hirschhorn Syndrome.

Journal of Medical Genetics

English

Chromosome 22q11 Microdeletions in Tetralogy of Fallot.

Archives of Disease in Childhood

English

Y Chromosome Microdeletions Screening in Tunisian Infertile Men

Annales de Biologie Clinique

Molecular Biology

English

A Study of Y Chromosome Microdeletions in Infertile Indian Males

International Journal of Human Genetics

English

Disomy 21 in Spermatozoa and the Paternal Origin of Trisomy 21 Down Syndrome

Molecular Cytogenetics

Molecular Medicine

Molecular Biology

English

Paternal Uniparental Disomy of Chromosome 13

English

Sotos Syndrome: A Case Report

Turkish Journal of Pediatric Disease

English

Paternal Uniparental Disomy of Chromosome 1

English

Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, With Homoallelism for Mutations in RPE65 or MERTK, Respectively

American Journal of Human Genetics

English