Kallmann Syndrome and the Link between Olfactory and Reproductive Development

Author:

Rugarli Elena I.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference41 articles.

1. Deletions and translocations involving the distal short arm of the human X chromosome: review and hypotheses;Ballabio;Hum Mol Genet,1992

2. Ballabio A, Rugarli EI. Kallmann syndrome. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular bases of inherited disease. McGraw-Hill, New York (in press)

3. Kallmann syndrome, spinocerebellar ataxia type 1, Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies, Waardenburg syndrome, Pelizaeus-Merzbacher disease, Norrie disease, neurofibromatosis 2;Ballabio,1995

4. The functionality of the human vomeronasal organ (VNO): evidence for steroid receptors;Berliner;J Steroid Biochem Mol Biol,1996

5. Bringing Kallmann syndrome into focus;Bick;Am J Neuroradiol,1993

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