Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

BACKGROUND: A marker chromosome is defined as a structurally abnormal chromosome that cannot be identified by routine cytogenetics. The risk for phenotypic abnormalities associated with a marker chromosome depends on several factors, including inheritance, mode of ascertainment, chromosomal origin,...

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Bibliografische gegevens
Hoofdauteurs: Graf, M D, Christ, L, Mascarello, J T, Mowrey, P, Pettenati, M, Stetten, G, Storto, P, Surti, U, Van Dyke, D L, Vance, G H, Wolff, D, Schwartz, S
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: BMJ Group 2006
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Original Article
Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2564588/
https://ncbi.nlm.nih.gov/pubmed/16882740
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2005.037887
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