Medlineplus phenylketonuria
February 27th 2008
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Medlineplus phenylketonuria
Phenylketonuria - OrganizedWisdom Health
InteliHealth: What is it? MedlinePlus: Phenylketonuria; Wikipedia: Phenylketonuria; National Institure of Child Health & Human Development: What is Phenylketonuria? MedicineNet: What is ... (more...)
Phenylketonuria, Maternal
National Library of Medicine - Medical Subject Headings 2003 MeSH MeSH Descriptor Data (more...)
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Phenylketonuria
Maternal
Phenylketonuria - Wikipedia, the free encyclopedia
DiseasesDB: 9987: MedlinePlus: 001166: eMedicine: ped/1787 derm/712: MeSH: D010661 ... Phenylketonuria (PKU) is an autosomal recessive genetic disorder characterized by a deficiency ... (more...)
genome.gov | Learning About Phenylketonuria
From Medline Plus; Phenylketonuria [nlm.nih.gov] From Medline Plus Medical Encyclopedia; California Coalition for PKU and Allied Disorders [ccpkuad.org] (more...)
WIC Works Topics A - Z
Genetics Home Reference, National Library ofMedicine. Phenylketonuria - MedlinePlus Medical Encyclopedia. Newborn Screening Factsheet ... (more...)
MedlinePlus Medical Encyclopedia: Phenylketonuria
Definition, causes, symptoms and treatment. (more...)
Phenylketonuria - Genetics Home Reference
GeneReviews; Genetic Alliance; MedlinePlus Encyclopedia: Phenylketonuria; MedlinePlus Encyclopedia: Serum Phenylalanine Screening; You might also find information on treatment of ... (more...)
TauMed - Phenylketonuria Community
MedlinePlus: Phenylketonuria Phenylketonuria (PKU) is a genetic disorder in which the body can't process part of a protein called phenylalanine (Phe). (more...)
MedlinePlus: Phenylketonuria
National Institutes of Health. The primary NIH organization for research on Phenylketonuria is the National Institute of Child Health and Human Development (more...)
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Phenylketonuria
Phenylketonuria (PKU) / Family Village Library
Who to Contact. Children's PKU Network 3790 Via De La Valle, Ste 120 Del Mar, CA ... QUE ES LA FENILCETONURIA? MEDLINEplus: Phenylketonuria. Phenylketonuria article and bibliography from OMIM (more...)