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Impact of medical genetics concerning phenylketonuria : accomplishments, status and practical future possibilitiesGUTTLER, F.Clinical genetics. 1989, Vol 36, Num 5, pp 333-334, issn 0009-9163, 2 p.Conference Paper

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ATTUALI VEDUTE SUL TRATTAMENTO DIETETICO DELLA FENILCHETONURIA = LES CONCEPTIONS ACTUELLES DU TRAITEMENT DIETETIQUE DES PHENYLCETONURIEGIOVANNINI M; RIVA E; ROSASCHINO F et al.1972; MINERVA PEDIATR.; ITAL.; DA. 1972; VOL. 24; NO 23; PP. 970-975; ABS. ANGL.; BIBL. 18 REF.Serial Issue

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PHENYL-KETONURIA AS A BALANCED POLYMORPHISM: THE NATURE OF THE HETEROZYGOTE ADVANTAGE = LA PHENYLCETONURIE, POLYMORPHISME BALANCE: NATURE DE L'AVANTAGE HETEROZYGOTEWOOLF LI; MCBEAN MS; WOOLF FM et al.1975; ANN. HUM. GENET.; G.B.; DA. 1975; VOL. 38; NO 4; PP. 461-469; BIBL. 1 P.Article

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DETECTION OF HEPATIC PHENYLALANINE4-HYDROXYLASE IN CLASSICAL PHENYLKETONURIA = DETECTION DE PHENYLALANINE 4-HYDROXYLASE HEPATIQUE DANS LA PHENYLCETONURIE CLASSIQUEFRIEDMAN PA; FISHER DB; KANG ES et al.1973; PROC. NATION. ACAD. SCI. U.S.A.; U.S.A.; DA. 1973; VOL. 70; NO 2; PP. 552-556; BIBL. 25REF.Serial Issue

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