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/vufind/Search/Results?lookfor=%22McGown%2C+Ivan%22&type=Person&page=3
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PubPharm (29)
21
Utility of AVP gene testing in familial neurohypophyseal diabetes insipidus
enthalten in:
Clinical endocrinology
| 2008
von
Chitturi, S.
|
Harris, M.
|
Thomsett, M.
| +6
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22
Paediatric diabetes--which children can gain insulin independence?
enthalten in:
The Medical journal of Australia
| 2007
von
Harris, M.
|
McGown, I.
|
Cowley, D.
CommentOn: Med J Aust. 2007 May 7;186(9):436-7. - PMID 17484702
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23
Autopsy Diagnosis of 21-Hydroxylase Deficiency CAH in a Case of Apparent SIDS
enthalten in:
Pediatric and developmental pathology
| 2005
von
Gozzi, T.
|
Harris, N.
|
McGown, I.
| +5
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24
Autopsy Diagnosis of 21-Hydroxylase Deficiency CAH in a Case of Apparent SIDS
enthalten in:
Pediatric and developmental pathology
| 2005
von
Gozzi, T.
|
Harris, N.
|
McGown, I.
| +5
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25
Autopsy Diagnosis of 21-Hydroxylase Deficiency CAH in a Case of Apparent SIDS
enthalten in:
Pediatric and developmental pathology
| 2005
von
Gozzi, T.
|
Harris, N.
|
McGown, I.
| +5
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26
Autopsy diagnosis of 21-hydroxylase deficiency CAH in a case of apparent SIDS
enthalten in:
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society
| 2005
von
Gozzi, T.
|
Harris, N.
|
McGown, I.
| +5
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27
Two novel mutant human adenylosuccinate lyases (ASLs) associated with autism and characterization of the equivalent mutant Bacillus subtilis ASL
enthalten in:
The Journal of biological chemistry
| 2004
von
Sivendran, S.
|
Patterson, D.
|
Spiegel, E.
| +3
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28
Two Novel Mutant Human Adenylosuccinate Lyases (ASLs) Associated with Autism and Characterization of the Equivalent Mutant Bacillus subtilis ASL
enthalten in:
The journal of biological chemistry
| 2004
von
Sivendran, S.
|
Patterson, D.
|
Spiegel, E.
| +3
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29
Maternal Gonadal Mosaicism Causing Ornthine Transcarbamylase Deficiency
enthalten in:
American journal of medical genetics
| 1999
von
Bowling, F.
|
McGown, I.
|
McGill, J.
| +2
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Journal of inherited metabolic disease
3
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International journal of pediatric endocrinology
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21-hydroxylase deficiency
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3
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High Performance Liquid Chromatography
3
Myoclonic Jerk
3
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3
Severe Psychomotor Retardation
3
congenital adrenal hyperplasia
3
neonatal screening
3
sudden infant death syndrome
2
19240-42-7
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415SHH325A
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4542-23-8
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7LP2MPO46S
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Adenosine
2
Adenosine Monophosphate
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