Linked Life Data

11119745

Source:http://linkedlifedata.com/resource/pubmed/id/11119745

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2001-1-2
pubmed:abstractText
To evaluate relationships between the phenotypic and genotypic characteristics of patients with congenital bilateral absence of the vas deferens (CBAVD).
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0015-0282
pubmed:author
pubmed:issnType
Print
pubmed:volume
74
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1164-74
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:11119745-Abnormalities, Multiple, pubmed-meshheading:11119745-Adult, pubmed-meshheading:11119745-Alleles, pubmed-meshheading:11119745-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:11119745-Fructose, pubmed-meshheading:11119745-Genetic Counseling, pubmed-meshheading:11119745-Genotype, pubmed-meshheading:11119745-Humans, pubmed-meshheading:11119745-Kidney, pubmed-meshheading:11119745-Male, pubmed-meshheading:11119745-Mutation, pubmed-meshheading:11119745-Osmolar Concentration, pubmed-meshheading:11119745-Phenotype, pubmed-meshheading:11119745-Retrospective Studies, pubmed-meshheading:11119745-Semen, pubmed-meshheading:11119745-Seminal Vesicles, pubmed-meshheading:11119745-Sperm Count, pubmed-meshheading:11119745-Testis, pubmed-meshheading:11119745-Vas Deferens
pubmed:year
2000
pubmed:articleTitle
Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling.
pubmed:affiliation
CECOS Midi-Pyrénées, Toulouse, France. daudin.m@chu-toulouse.fr
pubmed:publicationType
Journal Article