Evidence for a novel gene for familial febrile convulsions, FEB2 , linked to chromosome 19p in an extended family from the Midwest

By Schneider D.T.  

Human Molecular Genetics, Vol. 7, Iss. 1, 1998-01 ,pp. : 63-68

Oxford University Press

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The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration

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Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1659-1666

Oxford University Press

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Three‐generation family with novel contiguous gene deletion on chromosome 2p22 associated with thoracic aortic aneurysm syndrome

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American Journal Of Medical Genetics Part A, Vol. 176, Iss. 3, 2018-03 ,pp. : 560-569

John Wiley & Sons Inc

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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

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Localization of the Gene Responsible for Familial Benign Polycythemia to Chromosome 11q23

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Human Heredity, Vol. 49, Iss. 3, 1999-05 ,pp. : 129-132

Karger

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