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Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.
Blennow, E; Telenius, H; de Vos, D; Larsson, C; Henriksson, P; Johansson, O; Carter, N P; Nordenskjöld, M.
Afiliação
  • Blennow E; Department of Clinical genetics, Karolinska Hospital, Stockholm, Sweden.
Am J Hum Genet ; 54(5): 877-83, 1994 May.
Article em En | MEDLINE | ID: mdl-8178828
Two patients with specific and similar phenotypes were both found to have an unusual marker chromosome present in 70%-80% of their lymphocytes at routine cytogenetic examination. The marker chromosomes were isolated by flow sorting and were amplified by degenerate oligonucleotide-primed PCR. These libraries and a cosmid probe located at 15q26 were used to characterize the marker chromosomes by FISH. Both marker chromosomes were found to consist of duplicated chromosome material from the distal part of chromosome 15q and were identified as inv dup(15) (qter-->q23::q23-->qter) and inv dup(15) (qter-->q24::q24-->qter), respectively. Hence, the markers did not include any known centromere region, and no alpha-satellite DNA could be detected at the site of the primary constriction. Tetrasomy 15q may be a new syndrome, associated with a specific type of marker chromosome. In addition, further analyses of this type of marker chromosome might give new insight into the structure and function of the mammalian centromere.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cromossomos Humanos Par 15 / DNA Satélite / Aberrações Cromossômicas Tipo de estudo: Prognostic_studies Limite: Adult / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 1994 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Anormalidades Múltiplas / Cromossomos Humanos Par 15 / DNA Satélite / Aberrações Cromossômicas Tipo de estudo: Prognostic_studies Limite: Adult / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 1994 Tipo de documento: Article