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Author/Creator Corcos, J

1. Prenatal diagnosis of myopathy, encephalopathy, lactic acidosis, and stroke-like syndrome: contribution to understanding mitochondrial DNA segregation during human embryofetal development. Issue 10 (11th May 2006)

Authors:
Bouchet, C; Steffann, J; Corcos, J; Monnot, S; Paquis, V; Rötig, A; Lebon, S; Levy, P; Royer, G; Giurgea, I; Gigarel, N; Benachi, A; Dumez, Y; Munnich, A; Bonnefont, J P
Journal:
Journal of medical genetics
Issue:
Volume 43:Issue 10(2006)
Page Start:
788
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Stability of the m.8993T→G mtDNA mutation load during human embryofetal development has implications for the feasibility of prenatal diagnosis in NARP syndrome. Issue 10 (1st June 2007)

Authors:
Steffann, J; Gigarel, N; Corcos, J; Bonnière, M; Encha-Razavi, F; Sinico, M; Prevot, S; Dumez, Y; Yamgnane, A; Frydman, R; Munnich, A; Bonnefont, J P
Journal:
Journal of medical genetics
Issue:
Volume 44:Issue 10(2007)
Page Start:
664
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

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