Shinji Saitoh
0000-0001-6911-3351
Nagoya City University
150 papers found
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Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome
The GABAA receptor beta 3-subunit gene (GABRB3) as a candidate responsible for central nerve disturbances in Angelman syndrome (AS)
DNA-based diagnosis of Angelman syndrome and Prader-Willi syndrome
Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patients
Angelman Syndrome in Three Siblings: Characteristic Epileptic Seizures and EEG Abnormalities
Cortical reflex myoclonus associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS): A case report
Familial Angelman syndrome caused by imprinted submicroscopic deletion encompassing GABAA receptor β3-subunit gene
Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11–13) by YAC cloning and FISH analysis
Molecular characterization of a candidate-imprinted gene in Prader-Willi and Angelman syndromes
A BsaBl RFLP detected for probe pML34 [D15S9] on chromosome 15q
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