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P Lertrit

Showing results (1-10 of 21) with videos related to

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The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Update in molecular genetics: mitochondrial energy transduction disordersS Marzuki, H Sudoyo, P Lertrit
Human Genetics|November 1, 1992
Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathyP Lertrit, A S Noer, E Byrne, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|January 5, 2002
Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case reportO Sitburana, R Witoonpanich, S Phudhichareonrat, et al.
Genetics and Molecular Research : GMR|July 16, 2016
Exome sequencing in Thai patients with familial obesityS Kaewsutthi, J Santiprabhob, B Phonrat, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|March 24, 1999
Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patientP Lertrit, N Ruangvaravate, Y Trongpanich, et al.
American Journal of Human Genetics|January 1, 1993
mtDNA in congenital myotonic dystrophyD Thyagarajan, E Byrne, A S Noer, et al.
Acta Neurologica Scandinavica|January 1, 1993
Significance of mitochondrial DNA deletions in myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Mitochondrial genome analysis in Kearns-Sayre syndromeP Lertrit, L Atchaneeyasakul, V Devahastin, et al.
Annals of Neurology|November 1, 1991
Mitochondrial DNA sequence analysis in congenital myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.
Japanese Journal of Ophthalmology|January 5, 2002
Leber's hereditary optic neuropathy in ThailandW L Chuenkongkaew, P Lertrit, A Poonyathalang, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Update in molecular genetics: mitochondrial energy transduction disordersS Marzuki, H Sudoyo, P Lertrit
Human Genetics|November 1, 1992
Tissue segregation of a heteroplasmic mtDNA mutation in MERRF (myoclonic epilepsy with ragged red fibers) encephalomyopathyP Lertrit, A S Noer, E Byrne, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|January 5, 2002
Seizures in myoclonic epilepsy with ragged-red fibers detected by DNA analysis: a case reportO Sitburana, R Witoonpanich, S Phudhichareonrat, et al.
Genetics and Molecular Research : GMR|July 16, 2016
Exome sequencing in Thai patients with familial obesityS Kaewsutthi, J Santiprabhob, B Phonrat, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet|March 24, 1999
Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patientP Lertrit, N Ruangvaravate, Y Trongpanich, et al.
American Journal of Human Genetics|January 1, 1993
mtDNA in congenital myotonic dystrophyD Thyagarajan, E Byrne, A S Noer, et al.
Acta Neurologica Scandinavica|January 1, 1993
Significance of mitochondrial DNA deletions in myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health|January 1, 1995
Mitochondrial genome analysis in Kearns-Sayre syndromeP Lertrit, L Atchaneeyasakul, V Devahastin, et al.
Annals of Neurology|November 1, 1991
Mitochondrial DNA sequence analysis in congenital myotonic dystrophyD Thyagarajan, E Byrne, S Noer, et al.
Japanese Journal of Ophthalmology|January 5, 2002
Leber's hereditary optic neuropathy in ThailandW L Chuenkongkaew, P Lertrit, A Poonyathalang, et al.
Pageof 3