Correlates of language impairment in children with galactosaemia

Journal of Inherited Metabolic Disease

Volumn 31, Issue 4, 2008, Pages 524-532

  Potter, N L ^a,e   Lazarus, J A C ^b   Johnson, J M ^a   Steiner, R D ^c   Shriberg, L D ^d  

^a WASHINGTON STATE UNIVERSITY   (United States)

^b UNIVERSITY OF WISCONSIN MADISON   (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^d UNIVERSITY OF WISCONSIN MADISON   (United States)

^e NONE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CLINICAL ARTICLE; COGNITION; COGNITIVE DEFECT; COGNITIVE DEVELOPMENT; CONTROLLED STUDY; EDUCATION; FAMILY HISTORY; FEMALE; GALACTOSEMIA; GENOTYPE; HUMAN; INTELLIGENCE QUOTIENT; LANGUAGE ABILITY; LANGUAGE DISABILITY; MALE; MILK; PARENT; PERINATAL PERIOD; QUESTIONNAIRE; RISK FACTOR; SIBLING; SPEECH DISORDER;

ADOLESCENT; ANIMALS; CHILD; CHILD, PRESCHOOL; COGNITION; FAMILY HEALTH; FEMALE; GALACTOSEMIAS; GENOTYPE; HUMANS; INFANT NUTRITION PHYSIOLOGY; INFANT, NEWBORN; LANGUAGE DEVELOPMENT DISORDERS; MALE; MILK; PARENTS; POLYMORPHISM, SINGLE NUCLEOTIDE; RISK FACTORS; SOCIOECONOMIC FACTORS; SPEECH THERAPY; UTP-HEXOSE-1-PHOSPHATE URIDYLYLTRANSFERASE;

EID: 50149099800     PISSN: 01418955     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-008-0877-y     Document Type: Article

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