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searching for Kallmann syndrome 7 found (65 total)

Hypogonadotropic hypogonadism (1,754 words) [view diff] exact match in snippet view article find links to article

sex determining region Y-Box 10 (SOX10), GNRHR, GNRH1 and KISS1R. Kallmann syndrome results in a loss of smell (anosmia) and is associated with KAL1 mutations

CHD7 (1,571 words) [view diff] exact match in snippet view article find links to article

chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome". American Journal of Human Genetics. 83 (4): 511–9. doi:10.1016/j

Fibroblast growth factor 8 (2,175 words) [view diff] exact match in snippet view article find links to article

1038/sj.onc.1205663. PMID 12140757. GeneReviews/NCBI/NIH/UW entry on Kallmann syndrome FGF8 human gene location in the UCSC Genome Browser. FGF8 human gene

Anovulation (2,771 words) [view diff] exact match in snippet view article find links to article

deficiency of GnRH knows as idiopathic hypogonadotropic hypogonadism or, Kallmann syndrome if it is associated with anosmia. Infiltrative disease or tumors affecting

List of Spanish inventors and discoverers (2,806 words) [view diff] exact match in snippet view article find links to article

being one of the first scientists to recognize the disorder known as Kallmann syndrome. Severo Ochoa (1905–1993), doctor and biochemist, achieved the synthesis

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

Kallmann syndrome 2; 147950; FGFR1 Kallmann syndrome 3; 244200; PROKR2 Kallmann syndrome 4; 610628; PROK2 Kallmann syndrome 5; 612370; CHD7 Kallmann syndrome

List of human clusters of differentiation (467 words) [view diff] exact match in snippet view article find links to article

osteoglophonic dysplasia, squamous cell lung cancer and autosomal dominant Kallmann syndrome and may be associated with cleft lip and/or palate. Somatic mutations