A rare 3q13.31 microdeletion including GAP43 and LSAMP genes
Main Authors: | Gimelli, Stefania, Leoni, Massimiliano, Di Rocco, Maja, Caridi, Gianluca, Porta, Simona, Cuoco, Cristina, Gimelli, Giorgio, Tassano, Elisa |
---|---|
Format: | Online |
Language: | English |
Published: |
BioMed Central
2013
|
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3906914/ |
Similar Items
-
Interstitial 7q31.1 copy number variations disrupting IMMP2L gene are associated with a wide spectrum of neurodevelopmental disorders
by: Gimelli, Stefania, et al.
Published: (2014) -
Adult expression of a 3q13.31 microdeletion
by: Lowther, Chelsea, et al.
Published: (2014) -
Identification of an Interstitial 18p11.32-p11.31 Duplication Including the EMILIN2 Gene in a Family with Porokeratosis of Mibelli
by: Occella, Corrado, et al.
Published: (2013) -
Thrombocytopenia-absent radius (TAR) syndrome due to compound inheritance for a 1q21.1 microdeletion and a low-frequency noncoding RBM8A SNP: a new familial case
by: Tassano, Elisa, et al.
Published: (2015) -
Parental Imbalances Involving Chromosomes 15q and 22q May Predispose to the Formation of De Novo Pathogenic Microdeletions and Microduplications in the Offspring
by: Capra, Valeria, et al.
Published: (2013)