Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
3
pubmed:dateCreated
2001-10-11
pubmed:abstractText
In this report we present the clinical features and molecular and cytogenetic findings in a female with partial trisomy 14q. Molecular and cytogenetic studies allowed us to determine that the extra 14q material (of paternal origin) was translocated postzygotically onto the maternal X chromosome. Consequently, only the derivative X chromosome was inactivated, although inactivation apparently did not spread over the entire chromosome 14q. This partial inactivation makes the present case unusual, giving rise to phenotypic features absent in other patients with partial trisomy 14q, typically restricted to the distal part of the chromosome.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0009-9163
pubmed:author
pubmed:issnType
Print
pubmed:volume
60
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
206-11
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:11595022-Blotting, Southern, pubmed-meshheading:11595022-Chromosome Banding, pubmed-meshheading:11595022-Chromosomes, pubmed-meshheading:11595022-Chromosomes, Human, Pair 14, pubmed-meshheading:11595022-Cytogenetics, pubmed-meshheading:11595022-Dosage Compensation, Genetic, pubmed-meshheading:11595022-Facies, pubmed-meshheading:11595022-Fathers, pubmed-meshheading:11595022-Female, pubmed-meshheading:11595022-Humans, pubmed-meshheading:11595022-In Situ Hybridization, pubmed-meshheading:11595022-In Situ Hybridization, Fluorescence, pubmed-meshheading:11595022-Karyotyping, pubmed-meshheading:11595022-Male, pubmed-meshheading:11595022-Maternal Age, pubmed-meshheading:11595022-Models, Genetic, pubmed-meshheading:11595022-Mothers, pubmed-meshheading:11595022-Pedigree, pubmed-meshheading:11595022-Polymorphism, Genetic, pubmed-meshheading:11595022-Translocation, Genetic, pubmed-meshheading:11595022-Trisomy, pubmed-meshheading:11595022-X Chromosome
pubmed:year
2001
pubmed:articleTitle
Trisomy rescue by postzygotic unbalanced (X;14) translocation in a girl with dysmorphic features.
pubmed:affiliation
Unidad de Genética y Diagnóstico Prenatal, Hospital Universitario La Fe, Valencia, Spain. orellana_car@gva.es
pubmed:publicationType
Journal Article, Case Reports