ESPE Yearbook of Paediatric Endocrinology Search

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ESPE Yearbook of Paediatric Endocrinology Search

http://www.espeyearbook.org/search?q=mn-wakeling
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Loss-of-function variants in <em>TBC1D32</em> underlie syndromic hypopituitarism | ESPEYB17
Hietamaki J; Gregory LC; Ayoub S; Iivonen AP; Vaaralahti K; Liu X; Brandstack N; Buckton AJ; Laine T; Kansakoski J; Hero M; Miet
https://www.espeyearbook.org/ey/0017/ey0017.1-4.htm
Published: 2020-10-23

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ESPE Yearbook of Paediatric Endocrinology Search

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ESPE Yearbook of Paediatric Endocrinology Search

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De novo mutations in EIF2B1 affecting eif2 signaling cause neonatal/early-onset diabetes and transient hepatic dysfunction | ESPEYB17
De Franco E; Caswell R; Johnson MB; Wakeling MN; Zung A; Dung VC; Bich Ngoc CT; Goonetilleke R; Vivanco Jury M; El-Khateeb M; El
https://www.espeyearbook.org/ey/0017/ey0017.2-7.htm
Published: 2020-10-23

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ESPE Yearbook of Paediatric Endocrinology Search

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ESPE Yearbook of Paediatric Endocrinology Search

http://www.espeyearbook.org/search?q=se-flanagan
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ESPE Yearbook of Paediatric Endocrinology