ISSN 1662-4009 (online)

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Showing page 1 of results 1 - 10 of about 33 pages

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ESPE Yearbook of Paediatric Endocrinology Search

http://www.espeyearbook.org/search?q=s-flanagan
Published:

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ESPE Yearbook of Paediatric Endocrinology Search

http://www.espeyearbook.org/search?q=se-flanagan
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ESPEYB16 Volume Editors | ESPE Yearbook of Paediatric Endocrinology

http://www.espeyearbook.org/ey/0016/category/9
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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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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
Published: 2020-10-23

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Trisomy 21 is a cause of permanent neonatal diabetes that is autoimmune but not HLA associated | ESPEYB16
Johnson MB; De Franco E; Atma W; Greeley S; Letourneau LR; Gillespie K; DS-PNDM consortium International; Wakeling MN; Ellard S;
http://www.espeyearbook.org/ey/0016/ey0016.2-6.htm
Published: 2019-09-12

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Trisomy 21 is a cause of permanent neonatal diabetes that is autoimmune but not HLA associated | ESPEYB16
Johnson MB; De Franco E; Atma W; Greeley S; Letourneau LR; Gillespie K; DS-PNDM consortium International; Wakeling MN; Ellard S;
http://www.espeyearbook.org/ey/0016/ey0016.2-6
Published: 2019-09-12

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ESPEYB15 Volume Editors | ESPE Yearbook of Paediatric Endocrinology

http://www.espeyearbook.org/ey/0015/category/9
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ESPEYB15 Volume Editors | ESPE Yearbook of Paediatric Endocrinology

http://www.espeyearbook.org/ey/0015/category/18
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ESPEYB15 Volume Editors | ESPE Yearbook of Paediatric Endocrinology

http://www.espeyearbook.org/ey/0015/category/12
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