The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits

By Allan Andrea M.   Liang Xiaomin   Luo Yuping   Pak ChangHui   Li Xuekun   Szulwach Keith E.   Chen Dahua   Jin Peng   Zhao Xinyu  

Human Molecular Genetics, Vol. 17, Iss. 13, 2008-07 ,pp. : 2047-2057

Oxford University Press

Access to resources Recommend Favorite

A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein

By Bardoni Barbara   Schenck Annette   Mandel Jean Louis  

Human Molecular Genetics, Vol. 8, Iss. 13, 1999-12 ,pp. : 2557-2566

Oxford University Press

Access to resources Recommend Favorite

A novel human odorant-binding protein gene family resulting from genomic duplicons at 9q34: differential expression in the oral and genital spheres

By Lacazette Eric   Gachon Anne-Marie   Pitiot Gilles  

Human Molecular Genetics, Vol. 9, Iss. 2, 2000-01 ,pp. : 289-301

Oxford University Press

Access to resources Recommend Favorite

Myosin binding protein C1: a novel gene for autosomal dominant distal arthrogryposis type 1

By Gurnett Christina A.   Desruisseau David M.   McCall Kevin   Choi Ryan   Meyer Zachary I.   Talerico Michael   Miller Sara E.   Ju Jeong-Sun   Pestronk Alan   Connolly Anne M.   Druley Todd E.   Weihl Conrad C.   Dobbs Mathew B.  

Human Molecular Genetics, Vol. 19, Iss. 7, 2010-04 ,pp. : 1165-1173

Oxford University Press

Access to resources Recommend Favorite

Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q

By  

Human Molecular Genetics, Vol. 10, Iss. 9, 2001-04 ,pp. : 973-982

Oxford University Press

Access to resources Recommend Favorite