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Hellenic Endocrine Society, Hormones, 2(17), p. 269-273

DOI: 10.1007/s42000-018-0028-2

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A rare cause of neonatal hypoglycemia in two siblings: TBX19 gene mutation

Journal article published in 2018 by Edip Unal ORCID, Ruken Yıldırım, Funda Feryal Taş, Suat Tekin, Askin Sen, Yusuf Kenan Haspolat
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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