RFLP haplotyping and mutation analysis of the phenylalamine hydroxylase gene in Dutch phenylketonuria families

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Published in:Human genetics 1993, Vol.92 (6), p.588-592
Main Authors: MEIJER, H, JONGBLOED, R. J. E, HEKKING, M, SPAAPEN, L. J. M, GERAEDTS, J. P. M
Format: Article
Language:English
Subjects:
Aminoacid disorders
Biological and medical sciences
Errors of metabolism
Medical sciences
Metabolic diseases
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container_end_page 592
container_issue 6
container_start_page 588
container_title Human genetics
container_volume 92
creator MEIJER, H
JONGBLOED, R. J. E
HEKKING, M
SPAAPEN, L. J. M
GERAEDTS, J. P. M
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ispartof Human genetics, 1993, Vol.92 (6), p.588-592
issn 0340-6717
1432-1203
language eng
recordid cdi_pascalfrancis_primary_3818201
source Springer Online Journal Archives (Through 1996)
subjects Aminoacid disorders
Biological and medical sciences
Errors of metabolism
Medical sciences
Metabolic diseases
title RFLP haplotyping and mutation analysis of the phenylalamine hydroxylase gene in Dutch phenylketonuria families
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