Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Kiyokuni Miura
EstablishingSONin 21q22.11 as a Cause a New Syndromic Form of Intellectual Disability: Possible Contribution to Braddock-Carey Syndrome Phenotype
American Journal of Medical Genetics, Part A
Genetics
MRI Findings in Patients With Symptomatic Localization-Related Epilepsies Beginning in Infancy and Early Childhood
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Related publications
Xp11.22 Deletions Encompassing CENPVL1, CENPVL2, MAGED1 and GSPT2 as a Cause of Syndromic X-Linked Intellectual Disability
PLoS ONE
Multidisciplinary
Rare Non-Syndromic Intellectual Disability
A Non-Coding Variant in the 5ʹ UTR of DLG3 Attenuates Protein Translation to Cause Non-Syndromic Intellectual Disability
European Journal of Human Genetics
Genetics
Mutations in SNX14 Cause a Distinctive Autosomal-Recessive Cerebellar Ataxia and Intellectual Disability Syndrome
American Journal of Human Genetics
Genetics
TRAPPC9-related Autosomal Recessive Intellectual Disability: Report of a New Mutation and Clinical Phenotype
European Journal of Human Genetics
Genetics
Five New Cases of Syndromic Intellectual Disability Due to KAT6A Mutations: Widening the Molecular and Clinical Spectrum
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
Van Der Woude Syndrome - A Syndromic Form of Orofacial Clefting
Journal of Clinical and Experimental Dentistry
Dentistry
A Case Report of Familial 4q13.3 Microdeletion in Three Individuals With Syndromic Intellectual Disability
BMC Medical Genomics
Genetics
Volume Instabilities in the Mantle as a Possible Cause for Kimberlite Form
