Related content

Polymorphic insertions/deletions of both 1550nt and 100nt in two microsatellite-containing, LINE-related intronic regions of the rabbit -casein gene

By Hiripi L.   Devinoy E.   Rat P.   Baranyi M.   Fontaine M.L.   Bosze Z.  

Gene, Vol. 213, Iss. 1, 1998-06 ,pp. : 23-30

Elsevier

Access to resources Recommend Favorite

Genes Devoid of Full-Length Transposable Element Insertions are Involved in Development and in the Regulation of Transcription in Human and Closely Related Species

By Mortada Hussein   Vieira Cristina   Lerat Emmanuelle  

Journal of Molecular Evolution, Vol. 71, Iss. 3, 2010-09 ,pp. : 180-191

Springer Publishing Company

Access to resources Recommend Favorite

Human pigmentation genes: identification, structure and consequences of polymorphic variation

By Sturm R.A.   Teasdale R.D.   Box N.F.  

Gene, Vol. 277, Iss. 1, 2001-10 ,pp. : 49-62

Elsevier

Access to resources Recommend Favorite

A Common Set of at Least 11 Functional Genes Is Lost in the Majority of NF1 Patients with Gross Deletions

By Jenne D.E.   Tinschert S.   Stegmann E.   Reimann H.   Nurnberg P.   Horn D.   Naumann I.   Buske A.   Thiel G.  

Genomics, Vol. 66, Iss. 1, 2000-05 ,pp. : 93-97

Elsevier

Access to resources Recommend Favorite

Molecular epidemiology of sporadic breast cancer - The role of polymorphic genes involved in oestrogen biosynthesis and metabolism

By Mitrunen K.   Hirvonen A.  

Mutation Research/Reviews in Mutation Research, Vol. 544, Iss. 1, 2003-09 ,pp. : 9-41

Elsevier

Access to resources Recommend Favorite