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1.
Comparative functional analysis of two fibroblast growth factor receptor 1 (FGFR1) mutations affecting the same residue (R254W and R254Q) in isolated hypogonadotropic hypogonadism (IHH).
Gene
; 516(1): 146-51, 2013 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-23276709
2.
Can Kallmann syndrome be occasionally diagnosed during childhood? Genetic diagnosis in a child with associated renal agenesis and mirror movements.
Asian J Androl
; 11(4): 521-3, 2009 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-19234483
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