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American Journal of Human Genetics|July 1, 1992
Time and space clusters of the French-Canadian M1V phenylketonuria mutation in FranceS Lyonnet, D Melle, M de Braekeleer, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1994
[Mutations of RET proto-oncogene in Hirschsprung disease]S Lyonnet, P Edery, L M Mulligan, et al.
Nature|January 27, 1994
Mutations of the RET proto-oncogene in Hirschsprung's diseaseP Edery, S Lyonnet, L M Mulligan, et al.
Molecular Genetics and Metabolism|March 22, 2003
Impaired mitochondrial pyruvate importation in a patient and a fetus at riskM Brivet, A Garcia-Cazorla, S Lyonnet, et al.
European Journal of Medical Genetics|January 11, 2020
Fraser syndrome without cryptophthalmos: Two casesS Boussion, S Lyonnet, B Van Der Zwaag, et al.
Genomics|October 1, 1992
The gene for X-linked hydrocephalus maps to Xq28, distal to DXS52S Lyonnet, A Pelet, G Royer, et al.
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