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Results 1 - 10 of 106 for Rahman syndrome
  1. DNMT3A overgrowth syndrome 
    ... of the disorder in their family. Tatton-Brown-Rahman syndrome TBRS Genetic Testing Registry: Tatton-Brown-Rahman overgrowth ... National Organization for Rare Disorders (NORD) TATTON-BROWN-RAHMAN SYNDROME; TBRS PubMed Lemire G, Gauthier J, Soucy JF, ...
    https://medlineplus.gov/.../condition/dnmt3a-overgrowth-syndrome - Genetics
  2. DNMT3A gene 
    ... Toribe Y, Shimojima K, Yamamoto T. Tatton-Brown-Rahman syndrome due to 2p23 microdeletion. Am J Med Genet ... PubMed Ostrowski PJ, Tatton-Brown K. Tatton-Brown-Rahman Syndrome. 2022 Jun 30. In: Adam MP, Feldman J, ...
    https://medlineplus.gov/genetics/gene/dnmt3a - Genetics
  3. Patient support and advocacy groups 
    ... Support Organization for Trisomy in Australia Tatton Brown Rahman Syndrome Community Taylor Bugs Kisses Foundation Team Sanfilippo Foundation ...
    https://medlineplus.gov/about/general/genetics/supportadvocacygroups -
  4. Leigh syndrome 
    ... nlm.nih.gov/books/NBK320989/ Citation on PubMed Rahman S. Leigh syndrome. Handb Clin Neurol. 2023;194:43-63. doi: ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  5. Sotos syndrome 
    ... Citation on PubMed Tatton-Brown K, Cole TRP, Rahman N. Sotos Syndrome. 2004 Dec 17 [updated 2022 Dec 1]. In: ... Free article on PubMed Central Tatton-Brown K, Rahman N. Clinical features of NSD1-positive Sotos syndrome. Clin Dysmorphol. 2004 Oct;13(4):199-204. ...
    https://medlineplus.gov/genetics/condition/sotos-syndrome - Genetics
  6. NSD1 gene 
    ... on PubMed Central Tatton-Brown K, Cole TRP, Rahman N. Sotos Syndrome. 2004 Dec 17 [updated 2022 Dec 1]. In: ... D, Turkmen S, Cormier-Daire V, Irrthum A, Rahman N; Childhood Overgrowth Collaboration. Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations. ...
    https://medlineplus.gov/genetics/gene/nsd1 - Genetics
  7. Weaver syndrome 
    ... IK, Cole T, Seal S; Childhood Overgrowth Consortium; Rahman N. Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype. Am ... Nov 8. Citation on PubMed Tatton-Brown K, Rahman N. The NSD1 and EZH2 ... PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/weaver-syndrome - Genetics
  8. DICER1 gene 
    ... Houlston R, Stiller C, Stratton MR, Douglas J, Rahman N. DICER1 syndrome: clarifying the diagnosis, clinical features and management implications ...
    https://medlineplus.gov/genetics/gene/dicer1 - Genetics
  9. DICER1 syndrome 
    ... Houlston R, Stiller C, Stratton MR, Douglas J, Rahman N. DICER1 syndrome: clarifying the diagnosis, clinical features and management implications ...
    https://medlineplus.gov/genetics/condition/dicer1-syndrome - Genetics
  10. BAP1 tumor predisposition syndrome 
    ... L, Carlo MI, Hanson H, Cebulla C, Abdel-Rahman M. BAP1 Tumor Predisposition Syndrome. 2016 Oct 13 [updated 2024 Dec 5]. In: ... PubMed Rai K, Pilarski R, Cebulla CM, Abdel-Rahman MH. Comprehensive review of BAP1 tumor predisposition syndrome with report of two new cases. Clin Genet. ...
    https://medlineplus.gov/.../bap1-tumor-predisposition-syndrome - Genetics
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