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<ArticleSet><Article><Journal><PublisherName></PublisherName><JournalTitle>Journal of Research in Medical Sciences</JournalTitle><Issn>1735-1995</Issn><Volume>12</Volume><Issue>2</Issue><PubDate PubStatus="epublish"><Year>2007</Year><Month>06</Month><Day>11</Day></PubDate></Journal><ArticleTitle>Uniparental disomy resulting from heterozygous Robertsonian translocation (13q14q) in both parents</ArticleTitle><FirstPage>100</FirstPage><LastPage>103</LastPage><Language>EN</Language><AuthorList><Author><FirstName>Mir Davood</FirstName><LastName>Omrani</LastName><Affiliation>Department of Genetics, Uremia University of Medical Sciences. davood_omrani@umsu.ac.ir</Affiliation></Author><Author><FirstName>Soraya</FirstName><LastName>Saleh Gargari</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2006</Year><Month>11</Month><Day>28</Day></PubDate><PubDate PubStatus="accepted"><Year>2007</Year><Month>02</Month><Day>09</Day></PubDate><PubDate PubStatus="revised"><Year>2007</Year><Month>01</Month><Day>31</Day></PubDate></History><Abstract>Uniparental disomy (UPD) is a situation in which both members of a chromosome pair are inherited from one parent. This study has been conducted on a family with a five year-old healthy girl and a mentally retarded boy. The parents were first cousins and they both had Robertsonian translocation between their long arm of chromosome 13 and 14 [45, XY t (13q14q)]. Their affected son had a similar karyotype. Their daughter&amp;rsquo;s karyotype revealed the presence of a homozygous Robertsonian 13/14 translocation 44, XX t (13q14), t(13q14q). According to the clinical findings it is possible to conclude that the affected boy suffers from UPD.KEY WORDS: Robertsonian translocation, uniparental disomy, chromosome 14.</Abstract></Article></ArticleSet>
