1301943

Source:http://linkedlifedata.com/resource/pubmed/id/1301943

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0017337, umls-concept:C0031456, umls-concept:C0031485, umls-concept:C0282540, umls-concept:C0678227, umls-concept:C1442161
pubmed:issue	4
pubmed:dateCreated	1993-6-10
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Phenylalanine Hydroxylase
pubmed:status	MEDLINE
pubmed:issn	1059-7794
pubmed:author	pubmed-author:KleimanSS, pubmed-author:SchwartzGG, pubmed-author:ShilohYY, pubmed-author:WooS LSL
pubmed:issnType	Print
pubmed:volume	1
pubmed:geneSymbol	PAH
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	344-6
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:1301943-Base Sequence, pubmed-meshheading:1301943-Consanguinity, pubmed-meshheading:1301943-DNA, pubmed-meshheading:1301943-DNA Mutational Analysis, pubmed-meshheading:1301943-Ethnic Groups, pubmed-meshheading:1301943-Exons, pubmed-meshheading:1301943-Female, pubmed-meshheading:1301943-Humans, pubmed-meshheading:1301943-Israel, pubmed-meshheading:1301943-Male, pubmed-meshheading:1301943-Molecular Sequence Data, pubmed-meshheading:1301943-Pedigree, pubmed-meshheading:1301943-Phenylalanine Hydroxylase, pubmed-meshheading:1301943-Phenylketonurias, pubmed-meshheading:1301943-Repetitive Sequences, Nucleic Acid, pubmed-meshheading:1301943-Sequence Deletion
pubmed:year	1992
pubmed:articleTitle	A 22-bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family.
pubmed:affiliation	Department of Human Genetics, Sackler School of Medicine, Tel Aviv University, Ramat Aviv, Israel.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't