Related content

No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures

By Windemuth C.   Schulz H.   Saar K.   Gennaro E.   Bianchi A.   Zara F.   Bulteau C.   Kaminska A.   Ville D.   Cieuta C.   Nabbout-Tarantino R.   Prud'homme J.-F.   Dulac O.   Bate L.   Gardiner R.M.   Lindhout D.   Wienker T.F.   Janz D.   Sander T.  

Epilepsy Research, Vol. 51, Iss. 1, 2002-09 ,pp. : 23-29

Elsevier

Access to resources Recommend Favorite

Linkage analysis between childhood absence epilepsy and genes encoding GABA A and GABA B receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q

By Robinson R.   Taske N.   Sander T.   Heils A.   Whitehouse W.   Goutieres F.   Aicardi J.   Lehesjoki A.-E.   Siren A.   Laue Friis M.   Kjeldsen M.J.   Panayiotopoulos C.   Kennedy C.   Ferrie C.   Rees M.   Gardiner R.M.  

Epilepsy Research, Vol. 48, Iss. 3, 2002-02 ,pp. : 169-179

Elsevier

Access to resources Recommend Favorite

Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees

By Curtain R. P.   Lea R. A.   Tajouri L.   Haupt L. M.   Ovcaric M.   MacMillan J.   Griffiths L. R.  

Neurological Research, Vol. 27, Iss. 6, 2005-09 ,pp. : 647-652

Maney Publishing

Access to resources Recommend Favorite

The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups

By Colson Natalie   Lea Rod   Quinlan Sharon   MacMillan John   Griffiths Lyn  

Neurogenetics, Vol. 5, Iss. 2, 2004-06 ,pp. : 129-133

Springer Publishing Company

Access to resources Recommend Favorite

Characterization of an Autism-Associated Segmental Maternal Heterodisomy of the Chromosome 15q11–13 Region

By Kwasnicka-Crawford Dorota   Roberts Wendy   Scherer Stephen  

Journal of Autism and Developmental Disorders, Vol. 37, Iss. 4, 2007-04 ,pp. : 694-702

Springer Publishing Company

Access to resources Recommend Favorite