Analysis of DNA ligase IV mutations found in LIG4 syndrome patients: the impact of two linked polymorphisms

Author： Girard Pierre-Marie   Kysela Boris   Härer Christine J.   Doherty Aidan J.   Jeggo Penny A.  

Publisher： Oxford University Press

ISSN： 1460-2083

Source： Human Molecular Genetics, Vol.13, Iss.20, 2004-10, pp. : 2369-2376

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth

By  

Molecular Syndromology, Vol. 4, Iss. 4, 2013-04 ,pp. : 173-178

Karger

Access to resources Recommend Favorite

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes

By Belohradsky B.H.  

Human Molecular Genetics, Vol. 10, Iss. 25, 2001-12 ,pp. : 2917-2931

Oxford University Press

Access to resources Recommend Favorite

ABCA4 mutations causing mislocalization are found frequently in patients with severe retinal dystrophies

By Wiszniewski Wojciech  

Human Molecular Genetics, Vol. 14, Iss. 19, 2005-10 ,pp. : 2769-2778

Oxford University Press

Access to resources Recommend Favorite

Functional analysis of MSH6 mutations linked to kindreds with putative hereditary non-polyposis colorectal cancer syndrome

By Kariola R.   Raevaara T.E.   Lönnqvist K.E.   Nyström-Lahti M.  

Human Molecular Genetics, Vol. 11, Iss. 11, 2002-05 ,pp. : 1303-1310

Oxford University Press

Access to resources Recommend Favorite

Distribution of Two X-Linked Trinucleotide Polymorphisms in Greece

By  

Public Health Genomics, Vol. 4, Iss. 2, 2001-11 ,pp. : 125-128

Karger

Access to resources Recommend Favorite