Severe prenatal renal anomalies associated with mutations in HNF1B or PAX2 genes.
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R. Salomon | C. Antignac | U. Jensen | C. Thauvin-Robinet | R. Bouvier | C. Jeanpierre | J. Martinovic | T. Attié-Bitach | M. Mathieu | D. Gaillard | P. Dechelotte | B. Turlin | P. Loget | L. Heidet | V. Moriniére | N. Leporrier | Leire Madariaga | Marie-Claire Gübler