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Results 1 - 10 of 13 for FG syndrome
  1. FG syndrome 
    FG syndrome is a genetic condition that affects many parts of the body and occurs almost exclusively in males. "FG" represents the surname initials of the ...
    https://medlineplus.gov/genetics/condition/fg-syndrome - Genetics
  2. CASK-related intellectual disability 
    ... Related Disorders National Organization for Rare Disorders (NORD) FG SYNDROME 4; FGS4 INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  3. Hyaline fibromatosis syndrome 
    ... Rokicki D, Dal Peraro M, van der Goot FG. In-depth analysis of hyaline fibromatosis syndrome frameshift mutations at the same site reveal the ...
    https://medlineplus.gov/.../condition/hyaline-fibromatosis-syndrome - Genetics
  4. Sheldon-Hall syndrome 
    ... on PubMed Central Toydemir RM, Rutherford A, Whitby FG, Jorde LB, Carey JC, Bamshad MJ. Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome. Nat Genet. 2006 May; ...
    https://medlineplus.gov/genetics/condition/sheldon-hall-syndrome - Genetics
  5. KBG syndrome 
    ... Lo-Castro A, Brancati F, Digilio MC, Garaci FG, Bollero P, Alfieri P, Curatolo P. Neurobehavioral phenotype observed in KBG syndrome caused by ANKRD11 mutations. Am J Med Genet ...
    https://medlineplus.gov/genetics/condition/kbg-syndrome - Genetics
  6. Myhre syndrome 
    ... S, Keng WT, Murday V, Whiteford M, Dikkers FG, Sikkema-Raddatz B, van Essen T, Tolmie J. Clinical features and respiratory complications in Myhre syndrome. Eur J Med Genet. 2011 Nov-Dec;54( ...
    https://medlineplus.gov/genetics/condition/myhre-syndrome - Genetics
  7. Kallmann syndrome 
    ... Rubio Almanza M, Tome Fernandez-Ladreda M, Debray FG, Bours V, Beckers A. Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes. Front Endocrinol (Lausanne). 2014 Jul 9;5:109. ...
    https://medlineplus.gov/genetics/condition/kallmann-syndrome - Genetics
  8. Freeman-Sheldon syndrome 
    ... Citation on PubMed Toydemir RM, Rutherford A, Whitby FG, Jorde LB, Carey JC, Bamshad MJ. Mutations in embryonic myosin heavy chain (MYH3) cause Freeman-Sheldon syndrome and Sheldon-Hall syndrome. Nat Genet. 2006 May; ...
    https://medlineplus.gov/genetics/condition/freeman-sheldon-syndrome - Genetics
  9. Distal arthrogryposis type 1 
    ... SS, Brassington AM, Grannatt K, Rutherford A, Whitby FG, Krakowiak PA, Jorde LB, Carey JC, Bamshad M. Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes. Am J Hum Genet. 2003 Mar;72(3): ...
    https://medlineplus.gov/.../condition/distal-arthrogryposis-type-1 - Genetics
  10. Maffucci syndrome 
    ... IC, Leithner A, Streitburger A, Klenke FM, Gouin FG, Campanacci DA, ... syndrome: an international multicenter study of 161 patients. Oncologist. ...
    https://medlineplus.gov/genetics/condition/maffucci-syndrome - Genetics
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