Imprinting Status of 11p15 Genes in Beckwith-Wiedemann Syndrome Patients with CDKN1C Mutations

By Li M.   Squire J.   Shuman C.   Atkin J.   Pauli R.   Smith A.   Chitayat D.   Weksberg R.  

Genomics, Vol. 74, Iss. 3, 2001-06 ,pp. : 370-376

Elsevier

Access to resources Recommend Favorite

Molecular Cloning of a Novel Human Gene (D11S4896E) at Chromosomal Region 11p15.5

By Parker N.J.   Begley C.G.   Smith P.J.   Fox R.M.  

Genomics, Vol. 37, Iss. 2, 1996-10 ,pp. : 253-256

Academic Press

Access to resources Recommend Favorite

Human FRAG1 Encodes a Novel Membrane-Spanning Protein That Localizes to Chromosome 11p15.5, a Region of Frequent Loss of Heterozygosity in Cancer

By Lorenzi M.V.   Castagnino P.   Aaronson D.C.   Lieb D.C.   Lee C.C.   Keck C.L.   Popescu N.C.   Miki T.  

Genomics, Vol. 62, Iss. 1, 1999-11 ,pp. : 59-66

Elsevier

Access to resources Recommend Favorite

A fluorescent method for detecting low-grade 11patUPD mosaicism in Beckwith-Wiedemann syndrome

By Russo S.   Mencarelli M.   Cavalleri F.   Selicorni A.   Cogliati F.   Larizza L.  

Molecular and Cellular Probes, Vol. 17, Iss. 6, 2003-12 ,pp. : 295-299

Elsevier

Access to resources Recommend Favorite

Cloning and Characterization of a Gene (RFN22) Encoding a Novel Brain Expressed Ring Finger Protein (BERP) That Maps to Human Chromosome 11p15.5

By El-Husseini A.E.-D.   Fretier P.   Vincent S.R.  

Genomics, Vol. 71, Iss. 3, 2001-02 ,pp. : 363-367

Elsevier

Access to resources Recommend Favorite