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Results 1 - 2 of 2 for Kallmann syndrome 4
  1. Kallmann syndrome 
    ... of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet. 2003 Apr;33(4):463-5. doi: 10.1038/ng1122. Epub 2003 ... PubMed Central Kim SH. Congenital Hypogonadotropic Hypogonadism ... Future. Endocrinol Metab (Seoul). 2015 Dec;30(4):456-66. doi: 10.3803/EnM.2015.30. ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  2. Congenital fibrosis of the extraocular muscles 
    ... vocal cords; and a set of symptoms called Kallmann syndrome, which features delayed or absent puberty and an ...
    https://medlineplus.gov/...nital-fibrosis-of-the-extraocular-muscles - Genetics