Related content

Convergent extension movements and ciliary function are mediated by ofd1 , a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene

By Ferrante Maria I.   Romio Leila   Castro Silvia   Collins John E.   Goulding David A.   Stemple Derek L.   Woolf Adrian S.   Wilson Stephen W.  

Human Molecular Genetics, Vol. 18, Iss. 2, 2009-01 ,pp. : 289-303

Oxford University Press

Access to resources Recommend Favorite

The Oral-Facial-Digital Syndrome Type 1 (OFD1), a Cause of Polycystic Kidney Disease and Associated Malformations, Maps to Xp22.2-Xp22.3

By Feather Sally A.  

Human Molecular Genetics, Vol. 6, Iss. 7, 1997-07 ,pp. : 1163-1167

Oxford University Press

Access to resources Recommend Favorite

Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral‐facial‐digital syndrome type VI

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2132-2137

John Wiley & Sons Inc

Access to resources Recommend Favorite

X-linked cataract and Nance-Horan syndrome are allelic disorders

By Coccia Margherita   Brooks Simon P.   Webb Tom R.   Christodoulou Katja   Wozniak Izabella O.   Murday Victoria   Balicki Martha   Yee Harris A.   Wangensteen Teresia   Riise Ruth   Saggar Anand K.   Park Soo-Mi   Kanuga Naheed   Francis Peter J.   Maher Eamonn R.   Moore Anthony T.   Russell-Eggitt Isabelle M.   Hardcastle Alison J.  

Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. : 2643-2655

Oxford University Press

Access to resources Recommend Favorite

A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor

By Ramser Juliane  

Human Molecular Genetics, Vol. 14, Iss. 8, 2005-04 ,pp. : 1019-1027

Oxford University Press

Access to resources Recommend Favorite