Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.

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Clinical UGT1A1 Genetic Analysis in Pediatric Patients: Experience of a Reference Laboratory.

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http://www.wikidata.org/entity/Q53496198

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2017 nî lūn-bûn

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2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

@zh-hant

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Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

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Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

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type

Item

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Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

@en

Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

@nl

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Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

@en

Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

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P1476

Clinical UGT1A1 Genetic Analys ...... nce of a Reference Laboratory.

@en

P2093

Ann M Moyer

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Jennifer M Skierka

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John L Black

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Katrina E Kotzer

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Linnea M Baudhuin

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Michelle L Kluge

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P2860

Bilirubin neurotoxicity in preterm infants: risk and prevention

A method and server for predicting damaging missense mutations

Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome.

Management of hyperbilirubinemia in the newborn infant 35 or more weeks of gestation.

The Human Gene Mutation Database: building a comprehensive mutation repository for clinical and molecular genetics, diagnostic testing and personalized genomic medicine

Statistical features of human exons and their flanking regions.

Risk factors for neurotoxicity in newborns with severe neonatal hyperbilirubinemia.

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia.

Accuracy of clinical judgment in neonatal jaundice.

P2888

s40291-017-0265-0

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327-335

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scholarly article

P356

10.1007/S40291-017-0265-0

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P478

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2017-06-01T00:00:00Z

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28213806

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