Partial trisomy of chromosome 10(q22–q24) due to maternal insertional translocation (15;10)

Interchromosomal insertional translocations are rare chromosome rearrangements with an incidence of about 1:80,000 live births. We report on the clinical and cytogenetic findings of a newborn baby with partial trisomy 10q22–10q24 due to a maternal insertional translocation 15;10. Partial trisomy of...

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Veröffentlicht in:	American journal of medical genetics 2004-12, Vol.131A (2), p.190-193
Hauptverfasser:	Han, J.Y., Kim, K.H., Jun, H.J., Je, G.H., Glotzbach, C.D., Shaffer, L.G.
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - genetics Biological and medical sciences Chromosome aberrations Chromosomes, Human, Pair 10 Chromosomes, Human, Pair 15 FISH General aspects. Genetic counseling Humans In Situ Hybridization, Fluorescence Infant, Newborn insertional translocation intrauterine growth retardation Male Medical genetics Medical sciences partial trisomy 10q prenatal ascertainment Translocation, Genetic Trisomy
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