Case Reports
doi: 10.1007/BF00446626.
Partial trisomy 10p and familial translocation t(7;10)(p22;p12)
- PMID: 844878
- DOI: 10.1007/BF00446626
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Case Reports
Partial trisomy 10p and familial translocation t(7;10)(p22;p12)
Hum Genet.
.
Abstract
A girl with partial trisomy for the short arm of chromosome 10(p12leads to pter) due to mal chromosome segregation in the father 46,XY,t(7;10)(p22;p12) is described. The major abnormalities in this case are: mottled skin, mid-facial hypoplasia, low percentiles for weight, length, and head circumference, and club feet.
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