Rare interstitial deletion (2)(p11.2p13) in a child with pericentric inversion (2)(p11.2q13) of paternal origin.

Source:http://linkedlifedata.com/resource/pubmed/id/10533028

Am. J. Med. Genet. 1999 Nov 19 87 2 139-42

Download in:

View as

General Info

PMID
10533028