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Chromosome 16, trisomy 16q

Known as: Duplication 16q, Trisomy 16q 
National Institutes of Health

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2 relations

Broader (2)

Chromosomes, Human, Pair 16Trisomy

Papers overview

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Review
2004
Review
2004
De novo terminal deletion 7 p 22 . 1 pter in a child without craniosynostosis
We report a female with a deletion of 9p and concomitant duplication of 16q [46,XX,-9,+der(9),t(9;16)(p24;ql3)]. Parental… 
Review
1998
Review
1998
A case of de novo translocation 16;21: trisomy 16q phenotype and origin of the aberration.
A male newborn with severe congenital abnormalities is described with a de-novo translocation 16;21 resulting in trisomy 16q… 
Review
1987
Review
1987
Partial duplication 16q: report of two affected siblings resulting from a maternal translocation and literature review
Two siblings with a partial duplication 16q, born to a woman with a balanced translocation (6; 16), are described. The first… 
1980
1980
Trisomy 16q21»qter
SummaryA case of trisomy 16q secondary to a paternal 16/18 translocation is described. A comparison of this case with the few… 
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