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Results 1 - 10 of 14 for Richter syndrome
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  1. Typical Treatment of Chronic Lymphocytic Leukemia (American Cancer Society)  
    Chronic Lymphocytic Leukemia/Treatments and Therapies ... Chronic Lymphocytic Leukemia ... American Cancer Society ... Treatment options for people with CLL vary greatly, ...
    https://www.cancer.org/.../treating/treatment-by-risk-group.html - External Health Links
  2. PRICKLE1-related progressive myoclonus epilepsy with ataxia 
    ... Saifi GM, Lupski JR, Delague V, Megarbane A, Richter A, Leshinsky E, Berkovic SF. An autosomal recessive cerebellar ataxia syndrome with upward gaze palsy, neuropathy, and seizures. Neurology. ...
    https://medlineplus.gov/...rogressive-myoclonus-epilepsy-with-ataxia - Genetics
  3. TIMM8A gene 
    ... 0. Epub 2007 May 23. Citation on PubMed Richter D, Conley ME, Rohrer J, Myers LA, Zahradka K, Kelecic J, Sertic J, Stavljenic-Rukavina A. A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness. Pediatr ...
    https://medlineplus.gov/genetics/gene/timm8a - Genetics
  4. CREBBP gene 
    ... 17. Citation on PubMed Bartsch O, Schmidt S, Richter M, Morlot S, Seemanova E, Wiebe G, Rasi S. DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS. ...
    https://medlineplus.gov/genetics/gene/crebbp - Genetics
  5. Rubinstein-Taybi syndrome 
    ... 17. Citation on PubMed Bartsch O, Schmidt S, Richter M, Morlot S, Seemanova E, Wiebe G, Rasi S. DNA sequencing of CREBBP demonstrates mutations in 56% of patients with Rubinstein-Taybi syndrome (RSTS) and in another patient with incomplete RSTS. ...
    https://medlineplus.gov/genetics/condition/rubinstein-taybi-syndrome - Genetics
  6. BTK gene 
    ... on PubMed or Free article on PubMed Central Richter D, Conley ME, Rohrer J, Myers LA, Zahradka K, Kelecic J, Sertic J, Stavljenic-Rukavina A. A contiguous deletion syndrome of X-linked agammaglobulinemia and sensorineural deafness. Pediatr ...
    https://medlineplus.gov/genetics/gene/btk - Genetics
  7. ADNP gene 
    ... der Aa N. A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP. Nat Genet. 2014 Apr;46(4):380-4. doi: 10.1038/ng.2899. Epub 2014 Feb 16. Citation on PubMed or Free article on PubMed Central Malishkevich A, Leyk J, Goldbaum O, Richter-Landsberg C, Gozes I. ADNP/ADNP2 expression in ...
    https://medlineplus.gov/genetics/gene/adnp - Genetics
  8. Aromatase deficiency 
    ... PubMed Central Ludwikowski B, Heger S, Datz N, Richter-Unruh A, Gonzalez R. Aromatase deficiency: rare cause ...
    https://medlineplus.gov/genetics/condition/aromatase-deficiency - Genetics
  9. Expert reviewers 
    ... Naples, Italy Gabriele Richard GeneDx Gaithersburg, Maryland Andrea Richter CHU Sainte-Justine Centre de Recherche University of ... Ruhr University Bochum, Germany Shannon Wieloch Aicardi-Goutières Syndrome Association Crested Butte, CO Janey Wiggs Harvard Medical ...
    https://medlineplus.gov/about/general/genetics/expertreviewers -
  10. LHCGR gene 
    ... LHCGR NCBI Gene ClinVar Kossack N, Simoni M, Richter-Unruh A, Themmen AP, Gromoll J. Mutations in ...
    https://medlineplus.gov/genetics/gene/lhcgr - Genetics
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