Linkage Mapping in 29 Bardet-Biedl Syndrome Families Confirms Loci in Chromosomal Regions 11q13, 15q22.3-q23, and 16q21

By Bruford E.A.   Riise R.   Teague P.W.   Porter K.   Thomson K.L.   Moore A.T.   Jay M.   Warburg M.   Schinzel A.   Tommerup N.   Tornqvist K.   Rosenberg T.   Patton M.   Mansfield D.C.   Wright A.F.  

Genomics, Vol. 41, Iss. 1, 1997-04 ,pp. : 93-99

Academic Press

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The Cloning and Developmental Expression of Unconventional Myosin IXA (MYO9A) a Gene in the Bardet-Biedl Syndrome (BBS4) Region at Chromosome 15q22-q23

By Gorman S.W.   Haider N.B.   Grieshammer U.   Swiderski R.E.   Kim E.   Welch J.W.   Searby C.   Leng S.   Carmi R.   Sheffield V.C.   Duhl D.M.  

Genomics, Vol. 59, Iss. 2, 1999-07 ,pp. : 150-160

Elsevier

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Cloning of a Novel Human Neural Cell Adhesion Molecule Gene (NCAM2) That Maps to Chromosome Region 21q21 and Is Potentially Involved in Down Syndrome

By Paoloni-Giacobino A.   Chen H.   Antonarakis S.E.  

Genomics, Vol. 43, Iss. 1, 1997-07 ,pp. : 43-51

Academic Press

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A Novel C-Terminal Binding Protein (CTBP2) Is Closely Related toCTBP1,an Adenovirus E1A-Binding Protein, and Maps to Human Chromosome 21q21.3

By Katsanis N.   Fisher E.M.C.  

Genomics, Vol. 47, Iss. 2, 1998-01 ,pp. : 294-299

Elsevier

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Cloning of a Human Homolog of the Drosophila Enhancer of zeste Gene (EZH2) That Maps to Chromosome 21q22.2

By Chen H.   Rossier C.   Antonarakis S.E.  

Genomics, Vol. 38, Iss. 1, 1996-11 ,pp. : 30-37

Academic Press

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