About: A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria

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About: A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria Goto Sponge NotDistinct Permalink

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scientific article published on 01 October 1986

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 1986 (uk) im Oktober 1986 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 1986 (ast) scientific article published on 01 October 1986 (en)
publication date	wds:Q69622506-86AA7948-2EE3-442E-9DF5-8A56A01FDA1A
publication date	1986-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q69622506-AB3E5519-7624-4378-8839-EE978DA936C7
language of work or name	English
cites work	wds:Q69622506-165ECC7B-88AC-4BEB-88C0-908E3FAF62F7 wds:Q69622506-21AD9E44-DF60-44AF-AED4-F00A1129F5D0 wds:Q69622506-2DD9368A-F0B0-4000-98E8-8771825106B9 wds:Q69622506-3D932EE2-93D8-4ADA-A8F9-C941B4EA57BF wds:Q69622506-4B15183E-D5DD-4BC2-8B61-AAD09C9A45C4 wds:Q69622506-99107A00-8168-4530-AFBA-D94FB7912D61 wds:Q69622506-B7CFE6B8-5E88-4252-A1E7-DE15D84A1D38 wds:Q69622506-E4A15196-ECC6-4B35-B0BC-077F7ADA7807 wds:Q69622506-EB6265A3-13A1-4A2F-A553-30D7BCFBBBAC wds:Q69622506-FD12E713-858E-41C2-84CB-94F39374207F
cites work	Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria Detection of hepatic phenylalanine 4-hydroxylase in classical phenylketonuria Heterogeneity in Genetic Control of Phenylalanine Metabolism in Man Determination of heterozygosity for phenylketonuria on the amino acid analyzer Detection of Heterozygotes for Phenylketonuria by Column Chromatography and Discriminatory Analysis Detection of the heterozygous carriers of phenylketonuria Daily rhythms in the concentrations of various amino acids in human plasma Classic phenylketonuria: Diagnosis through heterozygote detection Heterozygote detection in phenylketonuria Effect of Aspartame Loading upon Plasma and Erythrocyte Amino Acid Levels in Phenylketonuric Heterozygotes and Normal Adult Subjects
author name string	wds:Q69622506-483E139D-9B01-4E9B-A784-8A938A0A6050 wds:Q69622506-7849439E-0A21-4987-8740-93127F488B00 wds:Q69622506-D3A51219-B783-4546-94C3-5F7FC93F620D wds:Q69622506-F2A63A61-4364-4769-9C57-E031D63E3EDB
author name string	B F Andrews M A Hilton J N Sharpe L G Hicks
rdfs:label	A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (en) A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (nl)
skos:prefLabel	A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (en) A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (nl)
name	A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (en) A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (nl)
title	wds:Q69622506-2651B8B9-F6CF-4410-8E5D-5B200C225C3B
title	A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria (en)
page(s)	wds:Q69622506-011647BE-E00C-41D5-97D6-E7DECEE2CAF1
page(s)	601-604
instance of	wds:Q69622506-CE645029-141A-446F-BBA6-1D2D02FE14F2
instance of	scholarly article
main subject	wds:Q69622506-81A066C5-A7B2-48E0-A42F-D188A7F0FEEE
main subject	heterozygosity
PubMed ID	wds:Q69622506-48A8E5BD-E76B-4B33-969C-14034D765F3D
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/3761073
PubMed ID	3761073
published in	wds:Q69622506-7A362BC4-6204-4DC8-B46F-65CEB7D54FE1
published in	The Journal of Pediatrics
issue	wds:Q69622506-28804990-3ECB-4DF2-B6F0-C75120E02502
volume	wds:Q69622506-37E3FAAD-7FAA-442D-9179-605E940088D2
issue	4
volume	109
DOI	wds:Q69622506-887DC95A-87D5-4789-BF6E-E2EDBFA2739D
DOI	http://dx.doi.org/10.1016/S0022-3476(86)80220-7
DOI	10.1016/S0022-3476(86)80220-7
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q69622506
is cites work of	A model of human phenylalanine metabolism in normal subjects and in phenylketonuric patients Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotes. Phenylketonuria: distribution of DNA diagnostic patterns in German families Phenylketonuria Scientific Review Conference: state of the science and future research needs Tyrosine monitoring in children with early and continuously treated phenylketonuria: results of an international practice survey. Progress in the identification of the heterozygote in phenylketonuria Heterozygous carriers of classical phenylketonuria in a sample of the turkish population: Detection by a spectrofluorimetric method Improved identification of heterozygotes for phenylketonuria using blood neopterin and biopterin.
is cites work of	wds:Q51597580-82187730-7617-4AB0-9409-02ABB09FA7A0 wds:Q46976615-DC122C24-15B4-4A8F-A43C-AA42ECCD1534 wds:Q38349899-D32DAB8F-F3F2-4888-BC3C-4C5C6FFF9C7A wds:Q45298394-2887C50A-E547-417A-81A7-208DDD1E9915 wds:Q51602705-594D4ED0-3093-49F4-9451-78C47F27FAD2 wds:Q24672434-F0C605C2-D06A-41C4-9991-5411398F9284 wds:Q51655060-2184DFCC-4987-481C-9B86-D74D8CF64471 wds:Q69916658-61D3B8F5-6A6C-45A2-9EE8-A41595C823A1

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