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Journal of Medical Genetics|September 13, 2005
Analysis of mtDNA variant segregation during early human embryonic development: a tool for successful NARP preimplantation diagnosisJ Steffann, N Frydman, N Gigarel, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|September 28, 2011
[Preimplantation diagnosis with HLA typing: birth of the first double hope child in France]F Lamazou, J Steffann, N Frydman, et al.Journal of Medical Genetics|May 13, 2006
Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal developmentC Bouchet, J Steffann, J Corcos, et al.Prenatal Diagnosis|August 9, 2001
Prenatal diagnosis of respiratory chain deficiency by direct mutation screeningJ Amiel, N Gigarel, A Benacki, et al.Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|August 31, 2006
[Preimplantation genetic diagnosis (PGD): results from a Parisian center]E Feyereisen, S Romana, V Kerbrat, et al.Nature Genetics|October 4, 2000
Nuclear gene OPA1, encoding a mitochondrial dynamin-related protein, is mutated in dominant optic atrophyC Delettre, G Lenaers, J M Griffoin, et al.Pageof 2