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Results 1 - 10 of 43 for Brunner syndrome
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  1. Monoamine oxidase A deficiency 
    ... cannot pass X-linked traits to their sons. Brunner syndrome Deficiency of monoamine oxidase A X-linked monoamine oxidase deficiency Genetic Testing Registry: Brunner syndrome Monoamine oxidase A deficiency National Organization for Rare ...
    https://medlineplus.gov/.../condition/monoamine-oxidase-a-deficiency - Genetics
  2. Feingold syndrome 
    ... each cell is sufficient to cause the disorder. Brunner-Winter syndrome Microcephaly-mesobrachyphalangy-tracheoesophageal fistula (MMT) syndrome Microcephaly-oculo- ...
    https://medlineplus.gov/genetics/condition/feingold-syndrome - Genetics
  3. Ohdo syndrome, Maat-Kievit-Brunner type 
    The Maat-Kievit-Brunner type of Ohdo syndrome is a rare condition characterized by intellectual disability and distinctive facial features. It has only been reported in males. ...
    https://medlineplus.gov/.../ohdo-syndrome-maat-kievit-brunner-type - Genetics
  4. Meier-Gorlin syndrome 
    ... Skidmore DL, Samuels ME, Hoefsloot LH, Knoers NV, Brunner HG, Jackson AP, Bongers EM. Meier-Gorlin syndrome genotype-phenotype studies: 35 individuals with pre-replication ...
    https://medlineplus.gov/genetics/condition/meier-gorlin-syndrome - Genetics
  5. Kleefstra syndrome 
    ... AW, Morrison N, Keijzers-Vloet ST, Hoischen A, Brunner HG, Tolmie J, Kleefstra T. Familial Kleefstra syndrome due to maternal somatic mosaicism for interstitial 9q34. ...
    https://medlineplus.gov/genetics/condition/kleefstra-syndrome - Genetics
  6. Robinow syndrome 
    ... or Free article on PubMed Central Roifman M, Brunner H, Lohr J, Mazzeu J, Chitayat D. Autosomal Dominant Robinow Syndrome. 2015 Jan 8 [updated 2019 Oct 3]. In: ...
    https://medlineplus.gov/genetics/condition/robinow-syndrome - Genetics
  7. 3-M syndrome 
    ... on PubMed van der Wal G, Otten BJ, Brunner HG, van der Burgt I. 3-M syndrome: description of six new patients with review of ...
    https://medlineplus.gov/genetics/condition/3-m-syndrome - Genetics
  8. PACS1 syndrome 
    ... BH, de Vries BB, Devriendt K, Hurles ME, Brunner HG; DDD study. Clinical delineation of the PACS1-related syndrome--Report on 19 patients. Am J Med Genet ...
    https://medlineplus.gov/genetics/condition/pacs1-syndrome - Genetics
  9. Koolen-de Vries syndrome 
    ... NV, van Kessel AG, Sistermans EA, Veltman JA, Brunner HG, de Vries BB. A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism. Nat Genet. ...
    https://medlineplus.gov/genetics/condition/koolen-de-vries-syndrome - Genetics
  10. Cantú syndrome 
    ... Vries P, Steehouwer M, Veltman JA, Robertson SP, Brunner HG, de Vries BB, Hoischen A. Cantu syndrome is caused by mutations in ABCC9. Am J ...
    https://medlineplus.gov/genetics/condition/cantu-syndrome - Genetics
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