Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation
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Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation
description
2017 nî lūn-bûn
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2017年の論文
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年学术文章
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2017年學術文章
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2017年學術文章
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name
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@en
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@nl
type
label
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@en
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@nl
prefLabel
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@en
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@nl
P2093
P2860
P356
P1476
Two Childhood Pheochromocytoma ...... mor: A Very Rare Manifestation
@en
P2093
Asude Durmaz
Aydilek Dağdeviren Çakır
Ayça Aykut
Hande Turan
Olcay Evliyaoğlu
P2860
P304
P356
10.4274/JCRPE.5078
P577
2017-10-12T00:00:00Z