Novel TBX3 mutation data in families with Ulnar–Mammary syndrome indicate a genotype–phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects
Vasco Meneghini(Vita-Salute San Raffaele University), Giorgio R. Merlo(University of Turin), Aliana Egeo(Dulbecco Telethon Institute), Sylvie Odent(Institut de génétique et de développement de Rennes), Natalia Platonova(University of Milan)
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