1973295

Source:http://linkedlifedata.com/resource/pubmed/id/1973295

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007320, umls-concept:C0026882, umls-concept:C0033053, umls-concept:C0039082, umls-concept:C0085973, umls-concept:C0332120, umls-concept:C1515568
pubmed:issue	4
pubmed:dateCreated	1990-8-13
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8106540
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	0197-3851
pubmed:author	pubmed-author:BarkasMM, pubmed-author:BrandNN, pubmed-author:GazitEE, pubmed-author:HarelYY, pubmed-author:LotanDD
pubmed:issnType	Print
pubmed:volume	10
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	257-60
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:1973295-Blotting, Southern, pubmed-meshheading:1973295-Female, pubmed-meshheading:1973295-Genetic Linkage, pubmed-meshheading:1973295-Humans, pubmed-meshheading:1973295-Mutation, pubmed-meshheading:1973295-Oculocerebrorenal Syndrome, pubmed-meshheading:1973295-Pedigree, pubmed-meshheading:1973295-Polymorphism, Restriction Fragment Length, pubmed-meshheading:1973295-Pregnancy, pubmed-meshheading:1973295-Prenatal Diagnosis, pubmed-meshheading:1973295-Renal Tubular Transport, Inborn Errors, pubmed-meshheading:1973295-X Chromosome
pubmed:year	1990
pubmed:articleTitle	Prenatal diagnosis of Löwe's syndrome: a case report with evidence of de novo mutation.
pubmed:affiliation	Division of Pediatrics, Obstetrics and Gynecology, Chaim Sheba Medical Center, Tel Hashomer, Israel.
pubmed:publicationType	Journal Article, Case Reports