Mapping of the Familial Infantile Myasthenia (Congenital Myasthenic Syndrome Type Ia) Gene to Chromosome 17p with Evidence of Genetic Homogeneity

By Christodoulou Kyproula   Tsingis Marios   Deymeer Feza   Serdaroglu Piraye   Ozdemir Coskun   Al-Shehab Ahmad   Bairactaris Chrysostomos   Mavromatis Ioannis   Mylonas Ioannis   Evoli Amelia   Kyriallis Kyriacos   Middleton Lefkos T.  

Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 635-640

Oxford University Press

Access to resources Recommend Favorite

Genetic Mapping and ENU Mutagenesis

By Beier David R.   Herron Bruce J.  

Genetica, Vol. 122, Iss. 1, 2004-09 ,pp. : 65-69

Springer Publishing Company

Access to resources Recommend Favorite

Strategies for genetic mapping of categorical traits

By Rao S.   Li X.  

Genetica, Vol. 109, Iss. 3, 2000-03 ,pp. : 183-197

Springer Publishing Company

Access to resources Recommend Favorite

The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)

By  

Molecular Syndromology, Vol. 2, Iss. 3-5, 2011-11 ,pp. : 186-201

Karger

Access to resources Recommend Favorite

QTL mapping and the genetic basis of adaptation: recent developments

By Zeng Zhao-Bang  

Genetica, Vol. 123, Iss. 1-2, 2005-02 ,pp. : 25-37

Springer Publishing Company

Access to resources Recommend Favorite