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- A CGG-Repeat Expansion Mutation inZNF713Causes FRA7A: Association with Autistic Spectrum Disorder in two Families Journal Articles
- A genome-wide association study of sporadic ALS in a homogenous Irish population Journal Articles
- Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia Journal Articles
- Genetic and Neurodevelopmental Influences in Autistic Disorder Journal Articles
- Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets Journal Articles
- Genomic organization of alpha satellite DNA on human chromosome 7: evidence for two distinct alphoid domains on a single chromosome. Journal Articles
- Holoprosencephaly, sacral anomalies, and situs ambiguus in an infant with partial monosomy 7q/trisomy 2p and SHH and HLXB9 haploinsufficiency Journal Articles
- Human Chromosome 7: DNA Sequence and Biology Journal Articles
- Radiation-induced genomic instability is associated with DNA methylation changes in cultured human keratinocytes Journal Articles
- Renal cell carcinoma with mixed features of papillary and clear cell cytomorphology: a fluorescent in situ hybridization study Journal Articles
- Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2 Journal Articles
- Trisomy 8 and 18 as frequent clonal and single-cell aberrations in 185 primary breast carcinomas Journal Articles