Infantile hyperinsulinism associated with enteropathy, deafness, and renal tubulopathy: A New Syndrome Caused By A Contiguous Gene Deletion Located On Chromosome 11.

Karen Cosgrove; Mark Dunne

Infantile hyperinsulinism associated with enteropathy, deafness, and renal tubulopathy: A New Syndrome Caused By A Contiguous Gene Deletion Located On Chromosome 11.

Karen Cosgrove
, Mark Dunne

Research output: Contribution to journal › Article › peer-review

Original language	English
Journal	Journal of Pediatric Endocrinology and Metabolism
Volume	17
Issue number	12
Publication status	Published - Dec 2004

Cite this

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title = "Infantile hyperinsulinism associated with enteropathy, deafness, and renal tubulopathy: A New Syndrome Caused By A Contiguous Gene Deletion Located On Chromosome 11.",

author = "Karen Cosgrove and Mark Dunne",

year = "2004",

month = dec,

language = "English",

volume = "17",

journal = "Journal of Pediatric Endocrinology and Metabolism",

publisher = "de Gruyter, Walter GmbH",

number = "12",

}

TY - JOUR

T1 - Infantile hyperinsulinism associated with enteropathy, deafness, and renal tubulopathy: A New Syndrome Caused By A Contiguous Gene Deletion Located On Chromosome 11.

AU - Cosgrove, Karen

AU - Dunne, Mark

PY - 2004/12

Y1 - 2004/12

M3 - Article

VL - 17

JO - Journal of Pediatric Endocrinology and Metabolism

JF - Journal of Pediatric Endocrinology and Metabolism

IS - 12

ER -