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6 in total

1. Microcephaly in a hyperphenylalaninemic infant leading to the diagnosis of maternal hyperphenylalaninemia.

Authors: N Gungor; A Tokath; T Coskun; M Ozguc; I Ozalp
Journal: Eur J Pediatr Date: 1996-03 Impact factor: 3.183

2. Phenylketonuria: variable phenotypic outcomes of the R261Q mutation and maternal PKU in the offspring of a healthy homozygote.

Authors: S Kleiman; L Vanagaite; J Bernstein; G Schwartz; N Brand; A Elitzur; S L Woo; Y Shiloh
Journal: J Med Genet Date: 1993-04 Impact factor: 6.318

3. Maternal non-phenylketonuric mild hyperphenylalaninemia.

Authors: H L Levy; S E Waisbren; D Lobbregt; E Allred; A Leviton; R Koch; W B Hanley; B Rouse; R Matalon; F de la Cruz
Journal: Eur J Pediatr Date: 1996-07 Impact factor: 3.183

4. The North American Maternal Phenylketonuria Collaborative Study, developmental assessment of the offspring: preliminary report.

Authors: W B Hanley; R Koch; H L Levy; R Matalon; B Rouse; C Azen; F de la Cruz
Journal: Eur J Pediatr Date: 1996-07 Impact factor: 3.183

5. Insurance coverage of special foods needed in the treatment of phenylketonuria.

Authors: B N Millner
Journal: Public Health Rep Date: 1993 Jan-Feb Impact factor: 2.792

6. Maternal phenylketonuria syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase Arg-261-Gln mutation.

Authors: A Superti-Furga; B Steinmann; G Duc; R Gitzelmann
Journal: Eur J Pediatr Date: 1991-05 Impact factor: 3.183

6 in total