Mutation analysis of the EMX2 gene in Kallmann’s syndrome

This publication has 47 references indexed in Scilit:

• CDX2, a human homologue of Drosophila caudal, is mutated in both alleles in a replication error positive colorectal cancer
  Oncogene, 1998
• Mutation of HOXA13 in hand-foot-genital syndrome
  Nature Genetics, 1997
• Bone loss in Kallmann syndrome
  Obstetrics & Gynecology, 1996
• Sex and smell – an enigma resolved
  Journal of Endocrinology, 1992
• The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules.
  Published by Elsevier ,1991
• A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules
  Nature, 1991
• Evidence that cells expressing luteinizing hormone-releasing hormone mRNA in the mouse are derived from progenitor cells in the olfactory placode.
  Proceedings of the National Academy of Sciences, 1989
• Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
  Proceedings of the National Academy of Sciences, 1989
• Origin of luteinizing hormone-releasing hormone neurons
  Nature, 1989
• The syndrome of anosmia with hypogonadotropic hypogonadism: A genetic study of 18 new families and a review
  American Journal of Medical Genetics, 1983