Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions - Concepedia

Concepedia

Publication | Open Access

Clinical phenotype of germline RUNX1 haploinsufficiency: from point mutations to large genomic deletions

DOI Full Paper Access

94

Citations

18

References

2008

Year

Mylène Béri‐Dexheimer, Véronique Latger‐Cannard, Christophe Philippe, Céline Bonnet, Pascal Chambon, Virginie Roth, Marie‐José Gregoire, Pierre Bordigoni, Thomas Lecompte, Bruno Leheup,

European Journal of Human Genetics

Allelic VariantPoint MutationsGenetic DisorderGeneticsGermline Runx1 HaploinsufficiencyPathologyMolecular GeneticsGermline GeneticsClinical PhenotypeGenomicsDisease Gene IdentificationMedicineClinical Genetics

References

	Year	Citations

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