Biallelic mutations in the prokineticin-2 gene in two sporadic cases of Kallmann syndrome

A gene deleted in Kallmann's syndrome shares homology with neural cell adhesion and axonal path-finding molecules

Brunella Franco, Silvana Guioli, Antonella Pragliola et al. · Nature · 1991 · 851 citations

Life Sciences, Genetics, Molecular Genetics +13

Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome

Catherine Dodé, Jacqueline Levilliers, Jean‐Michel Dupont et al. · Nature Genetics · 2003 · 830 citations

Life Sciences, Genetics, Molecular Genetics +9

The candidate gene for the X-linked Kallmann syndrome encodes a protein related to adhesion molecules

Renaud Legouis, Jean‐Pierre Hardelin, Jacqueline Levilliers et al. · Cell · 1991 · 684 citations

Life Sciences, Genetics, Molecular Genetics +8

The genetic aspects of primary eunuchoidism

Franz J. Kallmann · Medical Entomology and Zoology · 1944 · 661 citations

Life Sciences, Genetics, Medical Genetics +1

Luteinizing hormone-releasing hormone (LHRH)-expressing cells do not migrate normally in an inherited hypogonadal (Kallmann) syndrome

Marlene Schwanzel‐Fukuda, David Bick, Donald W. Pfaff · Molecular Brain Research · 1989 · 619 citations

Medicine, Endocrinology, Genetics +14