Isolation of Two Novel WNT Genes, WNT14 and WNT15, One of Which (WNT15) Is Closely Linked to WNT3 on Human Chromosome 17q21

By Bergstein I.   Eisenberg L.M.   Bhalerao J.   Jenkins N.A.   Copeland N.G.   Osborne M.P.   Bowcock A.M.   Brown A.M.C.  

Genomics, Vol. 46, Iss. 3, 1997-12 ,pp. : 450-458

Academic Press

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Isolation, characterisation and embryonic expression of WNT11, a gene which maps to 11q13.5 and has possible roles in the development of skeleton, kidney and lung

By Lako M.   Strachan T.   Bullen P.   Wilson D.I.   Robson S.C.   Lindsay S.  

Gene, Vol. 219, Iss. 1, 1998-09 ,pp. : 101-110

Elsevier

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Toward Cloning of a Novel Ataxia Gene: Refined Assignment and Physical Map of the IOSCA Locus (SCA8) on 10q24

By Nikali K.   Isosomppi J.   Lonnqvist T.   Mao J.I.   Suomalainen A.   Peltonen L.  

Genomics, Vol. 39, Iss. 2, 1997-01 ,pp. : 185-191

Academic Press

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The BTRC Gene, Encoding a Human F-Box/WD40-Repeat Protein, Maps to Chromosome 10q24-q25

By Fujiwara T.   Suzuki M.   Tanigami A.   Ikenoue T.   Omata M.   Chiba T.   Tanaka K.  

Genomics, Vol. 58, Iss. 1, 1999-05 ,pp. : 104-105

Elsevier

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Identification and characterization of a novel human brain-specific gene, homologous to S. scrofa tmp83.5, in the chromosome 10q24 critical region for temporal lobe epilepsy and spastic paraplegia

By Nobile C.   Hinzmann B.   Scannapieco P.   Siebert R.   Zimbello R.   Perez-Tur J.   Sarafidou T.   Moschonas N.K.   French L.   Deloukas P.   Ciccodicola A.   Gesk S.   Poza J.J.   Nigro C.L.   Seri M.   Schlegelberger B.   Rosenthal A.   Valle G.   de Munain A.L.   Tassinari C.A.   Michelucci R.  

Gene, Vol. 282, Iss. 1, 2002-01 ,pp. : 87-94

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