Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1974-1-16
pubmed:language
fre
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
0301-0171
pubmed:author
pubmed:issnType
Print
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
245-53
pubmed:dateRevised
2004-11-17
pubmed:meshHeading
pubmed-meshheading:4752866-Abnormalities, Multiple, pubmed-meshheading:4752866-Adult, pubmed-meshheading:4752866-Aneuploidy, pubmed-meshheading:4752866-Chromosome Aberrations, pubmed-meshheading:4752866-Chromosome Disorders, pubmed-meshheading:4752866-Chromosomes, Human, 6-12 and X, pubmed-meshheading:4752866-Craniofacial Dysostosis, pubmed-meshheading:4752866-Crossing Over, Genetic, pubmed-meshheading:4752866-Eyelids, pubmed-meshheading:4752866-Female, pubmed-meshheading:4752866-Genotype, pubmed-meshheading:4752866-Humans, pubmed-meshheading:4752866-Infant, pubmed-meshheading:4752866-Infant, Newborn, pubmed-meshheading:4752866-Karyotyping, pubmed-meshheading:4752866-Male, pubmed-meshheading:4752866-Microphthalmos, pubmed-meshheading:4752866-Phenotype, pubmed-meshheading:4752866-Recombination, Genetic
pubmed:year
1973
pubmed:articleTitle
[Pericentric inversion, inv(10), in a mother and aneusomy by recombination, inv(10), rec(10), in her son (author's transl)].
pubmed:publicationType
Journal Article