Is gene deletion in eukaryotes sequence-dependent? A study of nine deletion junctions and nineteen other deletion breakpoints in intron 7 of the human dystrophin gene

By McNaughton J.C.   Cockburn D.J.   Hughes G.   Jones W.A.   Laing N.G.   Ray P.N.   Stockwell P.A.   Petersen G.B.  

Gene, Vol. 222, Iss. 1, 1998-11 ,pp. : 41-51

Elsevier

Access to resources Recommend Favorite

The Evolution of an Intron: Analysis of a Long, Deletion-Prone Intron in the Human Dystrophin Gene

By McNaughton J.C.   Hughes G.   Jones W.A.   Stockwell P.A.   Klamut H.J.   Petersen G.B.  

Genomics, Vol. 40, Iss. 2, 1997-03 ,pp. : 294-304

Academic Press

Access to resources Recommend Favorite

A Novel Muscle-Specific Enhancer Identified within the Deletion Overlap Region of Two XLDC Patients Lacking Muscle Exon 1 of the Human Dystrophin Gene

By Bastianutto C.   de Visser M.   Muntoni F.   Klamut H.J.   Patarnello T.  

Genomics, Vol. 80, Iss. 6, 2002-12 ,pp. : 614-620

Academic Press

Access to resources Recommend Favorite

The human chromosomal gene for necdin, a neuronal growth suppressor, in the Prader-Willi syndrome deletion region

By Nakada Y.   Taniura H.   Uetsuki T.   Inazawa J.   Yoshikawa K.  

Gene, Vol. 213, Iss. 1, 1998-06 ,pp. : 65-72

Elsevier

Access to resources Recommend Favorite

Molecular Cloning and Chromosomal Localization of the Human Cyclin C (CCNC) and Cyclin E (CCNE) Genes: Deletion of the CCNC Gene in Human Tumors

By Li H.   Lahti J.M.   Valentine M.   Saito M.   Reed S.I.   Look A.T.   Kidd V.J.  

Genomics, Vol. 32, Iss. 2, 1996-03 ,pp. : 253-259

Academic Press

Access to resources Recommend Favorite