An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.

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An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.

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label

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.

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prefLabel

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria.

@en

P1476

An Efficient Trio-Based Mini-Haplotyping Method for Genetic Diagnosis of Phenylketonuria

@en

P2093

Aria Setoodeh

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Golnaz-Ensieh Kazemi-Sefat

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Masoumeh Razipour

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Mohammad Keramatipour

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Neda Mohajer

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Saeed Talebi

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Somayeh Ahmadloo

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P2860

Towards unbiased parentage assignment: combining genetic, behavioural and spatial data in a Bayesian framework.

Current trends in microsatellite genotyping.

Haplotypes and linkage disequilibrium at the phenylalanine hydroxylase locus, PAH, in a global representation of populations.

Phenylketonuria: an inborn error of phenylalanine metabolism.

PAHdb 2003: what a locus-specific knowledgebase can do.

Genotyping errors: causes, consequences and solutions.

Almost forgotten or latest practice? AFLP applications, analyses and advances.

The PAH gene, phenylketonuria, and a paradigm shift.

Regional mapping of the phenylalanine hydroxylase gene and the phenylketonuria locus in the human genome.

The influence of fluorescent dye structure on the electrophoretic mobility of end-labeled DNA

P304

229-236

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P31

scholarly article

P356

10.22074/CELLJ.2016.4318

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Mona Entezam

P577

2016-05-30T00:00:00Z

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P698

27540528

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P921

phenylketonuria

P932

4988422

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