Localization of a Gene for Oculodentodigital Syndrome to Human Chromosome 6q22–q24

By Gladwin Amanda   Donnai Dian   Metcalfe Kay   Schrander-Stumpel Connie   Brueton Louise   Verloes Alain   Aylsworth Arthur   Toriello Helga   Winter Robin   Dixon Michael  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 123-127

Oxford University Press

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Homozygosity Mapping of Alström Syndrome to Chromosome 2p

By Collin Gayle B.   Marshall Jan D.   Cardon Lon R.   Nishina Patsy M.  

Human Molecular Genetics, Vol. 6, Iss. 2, 1997-01 ,pp. : 213-219

Oxford University Press

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Fine-mapping the putative chromosome 17q21–22 prostate cancer susceptibility gene to a 10 cM region based on linkage analysis

By Lange Ethan   Robbins Christiane   Gillanders Elizabeth   Zheng Siqun   Xu Jianfeng   Wang Yunfei   White Kirsten   Chang Bao-Li   Ho Lindsey   Trent Jeffrey   Carpten John   Isaacs William   Cooney Kathleen  

Human Genetics, Vol. 121, Iss. 1, 2007-03 ,pp. : 49-55

Springer Publishing Company

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Linkage of the Gene for the Triple A Syndrome to Chromosome 12q13 Near the Type II Keratin Gene Cluster

By Weber Angela   Wienker Thomas F.   Jung Martin   Easton Douglas   Dean Heather J.   Heinrichs Claudine   Reis Andre   Clark Adrian J. L.  

Human Molecular Genetics, Vol. 5, Iss. 12, 1996-12 ,pp. : 2061-2066

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Genetic Linkage and Association Analysis for Loneliness in Dutch Twin and Sibling Pairs Points to a Region on Chromosome 12q23–24

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Behavior Genetics, Vol. 36, Iss. 1, 2006-01 ,pp. : 137-146

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