Functional dissection of sequence-specific NKX2-5 DNA binding domain mutations associated with human heart septation defects using a yeast-based system

By Inga Alberto  

Human Molecular Genetics, Vol. 14, Iss. 14, 2005-07 ,pp. : 1965-1975

Oxford University Press

Access to resources Recommend Favorite

Functional genetic analysis of mutations implicated in a human speech and language disorder

By Vernes Sonja C.   Nicod Jérôme   Coventry Julie A.   Kenny Niamh   Coupe Anne-Marie   Bird Louise E.   Davies Kay E.   Fisher Simon E.  

Human Molecular Genetics, Vol. 15, Iss. 21, 2006-11 ,pp. : 3154-3167

Oxford University Press

Access to resources Recommend Favorite

Overdosage of Hand2 causes limb and heart defects in the human chromosomal disorder partial trisomy distal 4q

By Tamura Masaru   Hosoya Masaki   Fujita Motoi   Iida Tomoko   Amano Takanori   Maeno Akiteru   Kataoka Taro   Otsuka Taketo   Tanaka Shigekazu   Tomizawa Shuichi   Shiroishi Toshihiko  

Human Molecular Genetics, Vol. 22, Iss. 12, 2013-06 ,pp. : 2471-2481

Oxford University Press

Access to resources Recommend Favorite

Somatic mutations in NKX2–5, GATA4, and HAND1 are not a common cause of tetralogy of Fallot or hypoplastic left heart

By  

American Journal Of Medical Genetics Part A, Vol. 155, Iss. 10, 2011-10 ,pp. : 2416-2421

John Wiley & Sons Inc

Access to resources Recommend Favorite

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome

By Luoma Petri T.  

Human Molecular Genetics, Vol. 14, Iss. 14, 2005-07 ,pp. : 1907-1920

Oxford University Press

Access to resources Recommend Favorite