Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families: case report (Q81675996)
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scientific article published on 21 April 2005
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families: case report |
scientific article published on 21 April 2005 |
Statements
Gonadotrophin therapy in Kallmann syndrome caused by heterozygous mutations of the gene for fibroblast growth factor receptor 1: report of three families: case report (English)
Naoko Sato
Tomonobu Hasegawa
Naoaki Hori
Maki Fukami
Yasunori Yoshimura
21 April 2005