A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2 - Concepedia

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A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2

DOI Full Paper Access

71

Citations

17

References

2006

Year

Katarina Lehmann, Petra Seemann, Jan H. Boergermann, G Morin, Silke Reif, Petra Knaus, Stefan Mundlos

European Journal of Human Genetics

BiologyGenetic DisorderNatural SciencesGeneticsMolecular BiologyMolecular GeneticsGenomicsMedicineNovel R486q MutationBrachydactyly Type A2

References

	Year	Citations

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