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- Contribution of SHANK3 mutations to autism spectrum disorder. Academic Article
- Genetic interaction between α4 and β2 subunits of high affinity nicotinic receptor: analysis in schizophrenia Academic Article
- Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2 Academic Article
- Genome-wide association studies identify loci associated with age at menarche and age at natural menopause Academic Article
- Genome-wide association study of emotional empathy in children Academic Article
- Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients Academic Article
- Linkage analysis of multiple endocrine neoplasia type 2A (MEN-2A) and three DNA markers on chromosome 20: Evidence against synteny Academic Article
- Localization and linkage of three polymorphic DNA sequences on human chromosome 20 Academic Article
- Multiple genes in human 20q13 chromosomal region are involved in an advanced prostate cancer xenograft. Academic Article
- Partial monosomy 1q43 and partial trisomy 20q13.2: a case report Academic Article
- Savant Characteristics in a Child with Developmental Delay and Deletion in the Short Arm of Chromosome 20 Academic Article
- pG95α1-7dIII/RI, a single copy clone at Xp11.4 which recognises a TaqI polymorphism (DXS209) Academic Article