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Results 1 - 10 of 11 for chen syndrome
  1. Chromosome 15 
    ... Cooper GM, Knight SJ, Romano C, Zuffardi O, Chen C, Schwartz CE, Eichler EE. A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures. Nat Genet. ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  2. Chromosome 17 
    ... on PubMed or Free article on PubMed Central Chen KS, Manian P, Koeuth T, Potocki L, Zhao Q, Chinault AC, Lee CC, Lupski JR. Homologous recombination of a flanking repeat gene cluster is a mechanism for a common contiguous gene deletion syndrome. Nat Genet. 1997 Oct;17(2):154-63. ...
    https://medlineplus.gov/genetics/chromosome/17 - Genetics
  3. Chromosome 3 
    ... K, Lundvall M, Blennow E. Distal 3p deletion syndrome: detailed molecular ... R, Wang J, Yu J, Sudbrak R, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, ...
    https://medlineplus.gov/genetics/chromosome/3 - Genetics
  4. X chromosome 
    ... Whittaker A, Deadman R, Carter NP, Hunt SE, Chen R, Cree A, Gunaratne P, Havlak P, Hodgson ... Carrel L, Chako J, Chapman JC, Chavez D, Chen E, Chen G, Chen Y, Chen Z, Chinault ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  5. Chromosome 12 
    ... on PubMed Scherer SE, Muzny DM, Buhay CJ, Chen R, Cree A, Ding Y, Dugan-Rocha S, ... CQ, Ansari-Lari MA, Ayele M, Brown MJ, Chen G, Chen Z, Clerc-Blankenburg KP, Davis C, ...
    https://medlineplus.gov/genetics/chromosome/12 - Genetics
  6. Chromosome 4 
    ... F, Hirschhorn K. The etiology of Wolf-Hirschhorn syndrome. Trends Genet. 2005 ... Citation on PubMed Chen CP, Chern SR, Lee CC, Chang TY, Wang ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics
  7. Chromosome 1 
    ... Regan R, Skinner C, Stevenson RE, Antonarakis SE, Chen C, Estivill X, Menten B, Gimelli G, Gribble ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  8. Chromosome 9 
    ... Burton J, Carder C, Carter NP, Chapman JC, Chen Y, Clarke G, Clark SY, Clee CM, Clegg ... DA, Stockton DW, Hudgins L. Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay. ...
    https://medlineplus.gov/genetics/chromosome/9 - Genetics
  9. Chromosome 18 
    ... National Human Genome Research Institute: Chromosome Abnormalities PubMed Chen H, Wang N, Huo Y, Sklar P, MacKinnon ...
    https://medlineplus.gov/genetics/chromosome/18 - Genetics
  10. Chromosome 10 
    ... Whitehead SL, Wilming L, Wray PW, Young L, Chen Y, Lovering RC, Moschonas NK, Siebert R, Fechtel ... Z, Ji Y, Luo Y. Chromosome 10q26 deletion syndrome: Two new cases and a review of the ...
    https://medlineplus.gov/genetics/chromosome/10 - Genetics
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