Prenatal diagnosis and prenatal imaging of a de novo 46,X,der(Y)t(X;Y)(p22.13;q11.23) leading to functional disomy for the distal end of the X chromosome short arm from Xp22.13 in a phenotypically male fetus with posterior fossa abnormalities.

Source:http://linkedlifedata.com/resource/pubmed/id/18925617

Download in:

View as

General Info

PMID
18925617