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Audrey Guilmatre

Showing results (11-20 of 15) with videos related to

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Leukemia|June 16, 2023
Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study groupLucille Lew-Derivry, Alice Marceau-Renaut, Laurène Fenwarth, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 27, 2018
Solid organ transplantation after hematopoietic stem cell transplantation in childhood: A multicentric retrospective surveyMaura Faraci, Alice Bertaina, Arnaud Dalissier, et al.
Human Mutation|June 5, 2010
Type I hyperprolinemia: genotype/phenotype correlationsAudrey Guilmatre, Solenn Legallic, Gary Steel, et al.
Archives of General Psychiatry|September 9, 2009
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationAudrey Guilmatre, Christèle Dubourg, Anne-Laure Mosca, et al.
Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Leukemia|June 16, 2023
Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study groupLucille Lew-Derivry, Alice Marceau-Renaut, Laurène Fenwarth, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|December 27, 2018
Solid organ transplantation after hematopoietic stem cell transplantation in childhood: A multicentric retrospective surveyMaura Faraci, Alice Bertaina, Arnaud Dalissier, et al.
Human Mutation|June 5, 2010
Type I hyperprolinemia: genotype/phenotype correlationsAudrey Guilmatre, Solenn Legallic, Gary Steel, et al.
Archives of General Psychiatry|September 9, 2009
Recurrent rearrangements in synaptic and neurodevelopmental genes and shared biologic pathways in schizophrenia, autism, and mental retardationAudrey Guilmatre, Christèle Dubourg, Anne-Laure Mosca, et al.
Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.
Pageof 2