Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
1996-3-14
pubmed:abstractText
Prader-Willi, Bardet-Biedl, Cohen, Borjeson and Wilson-Turner syndromes are genetic disorders characterized by obesity and other diverse abnormalities. These disorders have been mapped to their respective chromosomal regions, and we hypothesize that each region contains a gene or genes important in the regulation of body weight. We tested this hypothesis by genotyping sibling pairs (n = 207; 17 markers) from 44 families who were segregating an extreme obesity phenotype but were otherwise clinically normal. The number of alleles shared between siblings from these chromosomal regions did not correlate with similarity in body mass index (kg/m2). If genes in these regions contribute to non-syndromal obesity, the prevalence is low and the corresponding alleles are rare.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0307-0565
pubmed:author
pubmed:issnType
Print
pubmed:volume
19
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
599-603
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:8574268-Adult, pubmed-meshheading:8574268-Aged, pubmed-meshheading:8574268-Aged, 80 and over, pubmed-meshheading:8574268-Alleles, pubmed-meshheading:8574268-Body Mass Index, pubmed-meshheading:8574268-Body Weight, pubmed-meshheading:8574268-Chromosome Mapping, pubmed-meshheading:8574268-Chromosomes, pubmed-meshheading:8574268-DNA, pubmed-meshheading:8574268-Family Health, pubmed-meshheading:8574268-Female, pubmed-meshheading:8574268-Genes, Recessive, pubmed-meshheading:8574268-Genetic Linkage, pubmed-meshheading:8574268-Genotype, pubmed-meshheading:8574268-Humans, pubmed-meshheading:8574268-Hypogonadism, pubmed-meshheading:8574268-Intellectual Disability, pubmed-meshheading:8574268-Male, pubmed-meshheading:8574268-Middle Aged, pubmed-meshheading:8574268-Obesity, pubmed-meshheading:8574268-Phenotype, pubmed-meshheading:8574268-Polydactyly, pubmed-meshheading:8574268-Prader-Willi Syndrome, pubmed-meshheading:8574268-Questionnaires, pubmed-meshheading:8574268-Syndrome
pubmed:year
1995
pubmed:articleTitle
Human obesity does not segregate with the chromosomal regions of Prader-Willi, Bardet-Biedl, Cohen, Borjeson or Wilson-Turner syndromes.
pubmed:affiliation
Department of Psychiatry, University of Pennsylvania, Philadelphia 19104, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't