Millson_2012_Am.J.Med.Genet.A_158A_159

Reference

Title : Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability - Millson_2012_Am.J.Med.Genet.A_158A_159
Author(s) : Millson A , Lagrave D , Willis MJ , Rowe LR , Lyon E , South ST
Ref : American Journal of Medicine Genet A , 158A :159 , 2012
Abstract : Millson_2012_Am.J.Med.Genet.A_158A_159
ESTHER : Millson_2012_Am.J.Med.Genet.A_158A_159
PubMedSearch : Millson_2012_Am.J.Med.Genet.A_158A_159
PubMedID: 22106001

Related information

Citations formats

Millson A, Lagrave D, Willis MJ, Rowe LR, Lyon E, South ST (2012)
Chromosomal loss of 3q26.3-3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability
American Journal of Medicine Genet A 158A :159

Millson A, Lagrave D, Willis MJ, Rowe LR, Lyon E, South ST (2012)
American Journal of Medicine Genet A 158A :159