Phenylalanine hydroxylase

Results: 19



#Item
1Contribution of PAHs from coal–tar pavement sealcoat and other sources to 40 U.S. lakes

Contribution of PAHs from coal–tar pavement sealcoat and other sources to 40 U.S. lakes

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Source URL: tx.usgs.gov

Language: English - Date: 2010-12-01 10:31:59
2Syddansk Universitet  Splicing of phenylalanine hydroxylase (PAH) exon 11 is vulnerable - Molecular pathology of mutations in PAH exon 11 Heintz, Caroline; Dobrowolski, Steven F.; Andersen, Henriette Skovgaard; Demirkol,

Syddansk Universitet Splicing of phenylalanine hydroxylase (PAH) exon 11 is vulnerable - Molecular pathology of mutations in PAH exon 11 Heintz, Caroline; Dobrowolski, Steven F.; Andersen, Henriette Skovgaard; Demirkol,

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Source URL: findresearcher.sdu.dk

- Date: 2012-10-01 08:22:01
    3

    PDF Document

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    Source URL: www.pbs.gov.au

    Language: English - Date: 2014-10-01 21:56:22
    4In 1934, two severely mentally retarded children were brought by their mother to see Dr Asbjørn Følling, a Norwegian physician, having consulted numerous doctors to no avail. She had noticed that both children had a st

    In 1934, two severely mentally retarded children were brought by their mother to see Dr Asbjørn Følling, a Norwegian physician, having consulted numerous doctors to no avail. She had noticed that both children had a st

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    Source URL: www.ranzco.edu

    Language: English - Date: 2013-05-15 21:52:16
    5Retrospective: Seymour Kaufman (1924 –2009) BY LOUIS SOKOLOFF T

    Retrospective: Seymour Kaufman (1924 –2009) BY LOUIS SOKOLOFF T

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    Source URL: www.asbmb.org

    Language: English - Date: 2010-01-08 12:04:09
    6Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase

    Phenylketonuria (PKU) Phenylketonuria is a genetic disorder that is characterized by a person’s inability to utilize the essential amino acid, phenylalanine. A person with PKU lacks the enzyme phenylalanine hydroxylase

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    Source URL: www.sde.idaho.gov

    Language: English - Date: 2009-03-18 18:56:23
    7NIH PKU Conference: State of the Science and Future Research Needs Melissa A. Parisi Eunice Kennedy Shriver National Institute of Child Health and Human Development

    NIH PKU Conference: State of the Science and Future Research Needs Melissa A. Parisi Eunice Kennedy Shriver National Institute of Child Health and Human Development

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    Source URL: www.hrsa.gov

    Language: English - Date: 2014-12-04 01:13:32
    8Phenylketonuria (PKU)  (metabolic condition: amino acid disorder) Also known as:  •	 phenylalanine hydroxylase deficiency

    Phenylketonuria (PKU) (metabolic condition: amino acid disorder) Also known as: • phenylalanine hydroxylase deficiency

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    Source URL: www.albertahealthservices.ca

    Language: English - Date: 2013-09-16 18:35:23
    9(PKU) PHENYLKETONURIA Amino Acid Disorder Definition Phenylketonuria, or PKU, is an autosomal recessive defect in phenylalanine metabolism caused by the absence of the liver enzyme phenylalanine hydroxylase. Infants with

    (PKU) PHENYLKETONURIA Amino Acid Disorder Definition Phenylketonuria, or PKU, is an autosomal recessive defect in phenylalanine metabolism caused by the absence of the liver enzyme phenylalanine hydroxylase. Infants with

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    Source URL: www.idph.state.ia.us

    Language: English - Date: 2007-06-25 16:37:39
    10                             American  College  of  Medical  Genetics  ACT  SHEET Newborn Screening ACT Sheet

                                 American  College  of  Medical  Genetics  ACT SHEET Newborn Screening ACT Sheet

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    Source URL: www.babysfirsttest.org

    Language: English - Date: 2013-01-09 14:05:15