Maternal phenylketonuria syndrome: Congenital heart defects, microcephaly, and developmental outcomes

Journal of Pediatrics

Volumn 136, Issue 1, 2000, Pages 57-61

  Rouse, Bobbye ^a   Matalon, Reuben ^b   Koch, Richard ^b   Azen, Colleen ^b   Levy, Harvey ^b   Hanley, William ^b   Trefz, Frederick ^b   De La Cruz, Felix ^b  

^a University of Texas Medical Branch School of Medicine   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

PHENYLALANINE;

ADULT; ARTICLE; CONGENITAL HEART DISEASE; DIAGNOSTIC APPROACH ROUTE; DISEASE COURSE; DISEASE PREDISPOSITION; EARLY DIAGNOSIS; FEMALE; FOLLOW UP; GENE MUTATION; GENETIC RISK; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MICROCEPHALY; PHENYLKETONURIA; PRIORITY JOURNAL; RISK FACTOR;

EID: 0033941662     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3476(00)90050-7     Document Type: Article

References (18)

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