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Journal of Community Genetics|April 22, 2021
Our greatest untapped resource: our patientsMatt Bolz-Johnson, Tom Kenny, Yann Le Cam, et al.
International Archives of Medicine|May 13, 2008
Partial trisomy 13q22-qter associated to leukoencephalopathy and late onset generalised epilepsyRenee Ribacoba, Manuel Menendez-Gonzalez, Ines Hernando, et al.
Orphanet Journal of Rare Diseases|September 5, 2023
Together4RD position statement on collaboration between European reference networks and industryVictoria Hedley, Matt Bolz-Johnson, Ines Hernando, et al.
European Journal of Medical Genetics|September 24, 2005
High resolution microarray CGH and MLPA analysis for improved genotype/phenotype evaluation of two childhood genetic disorder cases: ring chromosome 19 and partial duplication 2qMario A J A Hermsen, Marianne Tijssen, Ines Hernando Acero, et al.
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