Fine mapping of the Schnyder’s crystalline corneal dystrophy locus

By Theendakara Veena   Tromp Gerard   Kuivaniemi Helena   White Peter   Panchal Seema   Cox Jennifer   Winters R.   Riebeling Petra   Tost Frank   Hoeltzenbein Maria   Tervo Timo   Henn Wolfram   Denniger Elke   Krause Matthias   Koksal Murat   Kargi Sebnem   Ugurbas Suat   Latvala Terho   Shearman Amanda   Weiss Jayne  

Human Genetics, Vol. 114, Iss. 6, 2004-05 ,pp. : 594-600

Springer Publishing Company

Access to resources Recommend Favorite

The Gene Responsible for Autosomal Dominant Doyne's Honeycomb Retinal Dystrophy ( DHRD ) Maps to Chromosome 2p16

By Gregory Cheryl Y.  

Human Molecular Genetics, Vol. 5, Iss. 7, 1996-01 ,pp. : 1055-1059

Oxford University Press

Access to resources Recommend Favorite

Localisation of a Gene for Central Areolar Choroidal Dystrophy to Chromosome 17p

By Lotery Andrew J.   Ennis Kevin T.   Silvestri Giuliana   Nicholl Suzanne   McGibbon David   Collins Alan D.   Hughes Anne E.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 705-708

Oxford University Press

Access to resources Recommend Favorite

Localisation of a Gene for Dominant Cone-Rod Dystrophy ( CORD6 ) to Chromosome 17p

By Kelsell Rosemary E.   Evans Kevin   Gregory Cheryl Y.   Moore Anthony T.   Bird Alan C.   Hunt David M.  

Human Molecular Genetics, Vol. 6, Iss. 4, 1997-01 ,pp. : 597-600

Oxford University Press

Access to resources Recommend Favorite

A Gene Responsible for a Sensorineural Nonsyndromic Recessive Deafness Maps to Chromosome 2p22–23

By Chaïb Hassan   Place Christophe   Salem Nabiha   Chardenoux Sébastien   Vincent Christophe   Weissenbach Jean   El-Zir Elie   Loiselet Jacques   Petit Christine  

Human Molecular Genetics, Vol. 5, Iss. 1, 1996-01 ,pp. : 155-158

Oxford University Press

Access to resources Recommend Favorite