Possible genes responsible for developmental delay observed in patients with rare 2q23q24 microdeletion syndrome: Literature review and description of an additional patient

Microdeletion 2q23.3q24.1: Exploring genotype-phenotype correlations

(2015) Donatella Milani et al.   CONGENITAL ANOMALIES

Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients

(2015) Keiko Shimojima et al.   CONGENITAL ANOMALIES

Microdeletion 2q23.3q24.1: Exploring genotype-phenotype correlations

(2015) Donatella Milani et al.   CONGENITAL ANOMALIES

Characteristics of 2p15-p16.1 microdeletion syndrome: Review and description of two additional patients

(2015) Keiko Shimojima et al.   CONGENITAL ANOMALIES

Intellectual Disability and HemizygousGPD2Mutation

(2013) Daniela Q.C.M. Barge-Schaapveld et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Genetic analysis ofNR4A2gene in a large population of Han Chinese patients with Parkinson's disease

(2012) H. Liu et al.   EUROPEAN JOURNAL OF NEUROLOGY

Association study of the KCNJ3 gene as a susceptibility candidate for schizophrenia in the Chinese population

(2011) Kazuo Yamada et al.   HUMAN GENETICS

Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment

(2009) Dianne F. Newbury et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

An 8.9 Mb 19p13 duplication associated with precocious puberty and a sporadic 3.9 Mb 2q23.3q24.1 deletion containing NR4A2 in mentally retarded members of a family with an intrachromosomal 19p-into-19q between-arm insertion

(2009) Helle Lybæk et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Haploinsufficiency of the GPD2 gene in a patient with nonsyndromic mental retardation

(2008) Hussein Daoud et al.   HUMAN GENETICS