Interstitial deletion of 2(q33q36) in a child with congenital abnormalities.
AUTOR(ES)
Gorski, J L
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1015586Documentos Relacionados
- Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a child with multiple congenital abnormalities.
- Interstitial deletion (6) (q11----q15) in an infant with congenital abnormalities.
- Change of blood group from A2 to Ax in a child with congenital abnormalities.
- Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.
- An unbalanced t(X;10) mat translocation in a child with congenital abnormalities.