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Public Health Genomics and Precision Health Knowledge Base (v10.0)
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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Nov 04, 2024
. (Total: 6390 publications)
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Records 1-5 (of 5 Records)
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Adrenoleukodystrophy[original query]
Implementation of newborn screening for conditions in the United States first recommended during 2010-2018
Singh S , Ojodu J , Kemper AR , Lam WKK ,
Grosse SD
.
Int J Neonatal Screen 2023 9 (2)
Newborn Screen for X-Linked Adrenoleukodystrophy Using Flow Injection Tandem Mass Spectrometry in Negative Ion Mode.
Teber TA , Conti BJ ,
Haynes CA
,
Hietala A , Baker MW .
Int J Neonatal Screen 2022 8 (2)
Newborn screening for X-linked adrenoleukodystrophy: evidence summary and advisory committee recommendation.
Kemper AR , Brosco J , Comeau AM , Green NS ,
Grosse SD
,
Jones E , Kwon JM , Lam WK , Ojodu J , Prosser LA , Tanksley S .
Genet Med 2016 19 (1) 121-126
Improved analysis of C26:0-lysophosphatidylcholine in dried-blood spots via negative ion mode HPLC-ESI-MS/MS for X-linked adrenoleukodystrophy newborn screening.
Haynes CA
,
De Jesus VR
.
Clin Chim Acta 2012 413 1217-21
Newborn bloodspot screening for lysosomal storage disorders.
Zhou H
,
Fernhoff P ,
Vogt RF
.
J Pediatr 2011 159 (1) 7-13 e1
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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