About: An atypical case of phenylketonuria

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scientific article published on 01 February 1951

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в лютому 1951 (uk) im Februar 1951 veröffentlichter wissenschaftlicher Artikel (de) 1951 թվականի փետրվարի 1-ին հրատարակված գիտական հոդված (hy) scientific article published on 01 February 1951 (en) artículu científicu espublizáu en febreru de 1951 (ast)
publication date	wds:Q75608172-601BC5B3-D415-4443-94C1-3E3AF8861DA4
publication date	1951-02-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q75608172-308F5FBA-01E6-4EDE-AC94-0F69F7A91349
language of work or name	English
cites work	wds:Q75608172-58548CE0-FA91-4AD5-A7FD-EEABD79216D3 wds:Q75608172-C63E56A1-B6B1-4B98-A2F8-4D7E2DE24B50
cites work	Phenylketonuria; a problem in eugenics Metabolic studies in phenylketonuria
author name string	wds:Q75608172-3C87A038-B606-4406-AB47-BE72F65743F3
author name string	V A COWIE
rdfs:label	An atypical case of phenylketonuria (en) An atypical case of phenylketonuria (nl) An atypical case of phenylketonuria (sq)
skos:prefLabel	An atypical case of phenylketonuria (en) An atypical case of phenylketonuria (nl) An atypical case of phenylketonuria (sq)
name	An atypical case of phenylketonuria (en) An atypical case of phenylketonuria (nl) An atypical case of phenylketonuria (sq)
title	wds:Q75608172-3A3233A9-2F46-430D-96E3-66884FA3AE74
title	An atypical case of phenylketonuria (en)
page(s)	wds:Q75608172-CDFCAF0E-CB1F-498B-83BA-B1E4D23BCA35
page(s)	272
instance of	wds:Q75608172-CD8B6D1D-878C-42EA-A957-7BB5AE16EE09
instance of	scholarly article
PubMed ID	wds:Q75608172-288BDF4A-4EAA-45E3-A90E-F05E0F045148
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/14795842
PubMed ID	14795842
published in	wds:Q75608172-FB794939-FA89-4D8E-8B1F-93DC847AECE4
published in	The Lancet
issue	wds:Q75608172-4D0F16AE-63B3-4495-B3C4-E098354AF8BA
volume	wds:Q75608172-9C979335-0EA1-44D5-AF5F-9E4B414391AC
issue	6649
volume	1
DOI	wds:Q75608172-D2849CAA-43BA-42D7-BA9B-AD7D14EE8312
DOI	http://dx.doi.org/10.1016/S0140-6736(51)93320-X
DOI	10.1016/S0140-6736(51)93320-X
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q75608172
is cites work of	Phenylketonuria and its variations. A review of recent developments Phenylketonuria with normal intelligence and Gowers' muscular dystrophy Atypical phenylketonuric heterozygote Phenylketonuria Testing - Its Role in Pediatrics and Public Health INHERITED METABOLIC DISORDERS: ERRORS OF PHENYLALANINE AND TYROSINE METABOLISM. Some aetiological problems in mental deficiency. 5-Hydroxytryptamine deficiency in phenylketonuria. A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninaemia) Recent studies on galactosaemia, phenylketonuria and homocystinuria Phenylketonuria: an unusual case Discussion on the AEtiology of Mental Defect [Abridged]
is cites work of	wds:Q34824818-384D880A-3598-406C-BFD3-43A4798F8924 wds:Q34226076-408501F0-4658-4EB4-B0AD-9E9699EC8D7B wds:Q35502573-4C80CD49-B7E6-4ED4-86AE-1C82EE08C24A wds:Q52167197-130960D5-F134-4DE0-A784-C6DD5A373D60 wds:Q41529811-7C51384B-11E5-4160-87E1-7996D378216F wds:Q78518564-52878878-DA6D-4088-A311-932CA1EAC39E wds:Q29029900-D461BE28-54B6-4A15-B9EB-CA7F79DC98A6 wds:Q70081031-FB24855A-BA2C-4594-8B42-1E834AD48191 wds:Q52144436-ADD08BEF-7149-49FE-A913-DBBEAEEAFC3D wds:Q39975602-49A89795-6892-41B6-B682-514C28979544 wds:Q85051058-EC3DDA66-81D7-49B5-B918-CC397F9D59E8

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