Jan Mohr

Physician, Deceased Person

1921 – 2009

16

Who was Jan Mohr?

Jan Gunnar Faye Mohr, was a Norwegian-Danish physician and geneticist, known for his discovery of the first cases of autosomal genetic linkage in man, between the Lutheran blood groups and the ABH-secretor system, and between these and the hereditary disease myotonic dystrophy. Besides being first steps in mapping the human genome, the findings illustrated the medical potential of linkage analysis in prenatal genetic diagnosis. Mohr is eponymously known by the syndrome Mohr-Tranebjærg, a progressive deafness with X-linked mode of inheritance, which was first described by Jan Mohr, and then more comprehensively by Tranebjærg et al. The 'Mohr syndrome', or oral-facial-digital syndrome type II, is named after Otto Lous Mohr, uncle of Jan Mohr.

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Born
Jan 10, 1921
Paris
Also known as
  • Dr. Jan Mohr
Nationality
  • Norway
  • Denmark
Profession
Died
Mar 17, 2009

Submitted
on July 23, 2013

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