Refinement of the Locus for Autosomal Dominant Hereditary Gingival Fibromatosis (GINGF) to a 3.8-cM Region on 2p21

By Xiao S.   Wang X.   Qu B.   Yang M.   Liu G.   Bu L.   Wang Y.   Zhu L.   Lei H.   Hu L.   Zhang X.   Liu J.   Zhao G.   Kong X.  

Genomics, Vol. 68, Iss. 3, 2000-09 ,pp. : 247-252

Elsevier

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Linkage Studies in a Large Kindred with Hereditary Pancreatitis Confirms Mapping of the Gene to a 16-cM Region on 7q

By Pandya A.   Blanton S.H.   Landa B.   Javaheri R.   Melvin E.   Nance W.E.   Markello T.  

Genomics, Vol. 38, Iss. 2, 1996-12 ,pp. : 227-230

Academic Press

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Refined Genetic and Physical Localization of the Wagner Disease (WGN1) Locus and the Genes CRTL1 and CSPG2 to a 2- to 2.5-cM Region of Chromosome 5q14.3

By Perveen R.   Hart-Holden N.   Dixon M.J.   Wiszniewski W.   Fryer A.E.   Brunner H.G.   Pinkners A.J.L.H.   van Beersum S.E.C.   Black G.C.M.  

Genomics, Vol. 57, Iss. 2, 1999-04 ,pp. : 219-226

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cDNA Cloning of a New Low-Density Lipoprotein Receptor-Related Protein and Mapping of Its Gene (LRP3) to Chromosome Bands 19q12-q13.2

By Ishii H.   Kim D.-H.   Fujita T.   Endo Y.   Saeki S.   Yamamoto T.T.  

Genomics, Vol. 51, Iss. 1, 1998-07 ,pp. : 132-135

Elsevier

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Definition of the Locus Responsible for Systemic Carnitine Deficiency within a 1.6-cM Region of Mouse Chromosome 11 by Detailed Linkage Analysis

By Okita K.   Tokino T.   Nishimori H.   Miura K.   Nikaido H.   Hayakawa J.I.   Ono A.   Kuwajima M.   Matsuzawa Y.   Nakamura Y.  

Genomics, Vol. 33, Iss. 2, 1996-04 ,pp. : 289-291

Academic Press

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