Common variants in the Trichohyalin gene are associated with straight hair in Europeans
- Dr Sarah E Medland, Queensland Institute of Medical Research, Brisbane, Australia, Australia
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Keratin 74 is a novel determinant of human hair texture and is mutated in autosomal dominant woolly hair
- Dr Yutaka Shimomura, Columbia University, United States
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Congenital generalized hypertrichosis is a genomic disorder
- Prof Xue Zhang, Chinese Academy of Medical Sciences & Peking Union Medical College, China
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A novel monilethrix mutation in the in Coil 2 of K86 causing autosomal dominant monilethrix with incomplete penetrance
- Dr Jack Green, St.Vincent's Hospital, Melbourne, Australia
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A novel mutation in the human hairless transcript gene in a family with Marie Unna hereditary hypotrichosis
- Dr Yuval Ramot, Hadassah- Hebrew University Medical Center, Israel
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Presentation of EHRS2011 in Jerusalem
- Prof Abraham Zlotogorski, Hadassah- Hebrew University Medical Center, Israel
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Discussion
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