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Results 1 - 10 of 11 for Partial deletion of chromosome 9
  1. Distal 18q deletion syndrome 
    ... Hale DE, Fox PT. Myelination in children with partial deletions of chromosome ... Genet A. 2006 Feb 15;140(4):331-9. doi: 10.1002/ajmg.a.31072. Citation on ...
    https://medlineplus.gov/.../condition/distal-18q-deletion-syndrome - Genetics
  2. Turner syndrome 
    ... chromosome mosaicism. Rarely, Turner syndrome caused by a partial deletion of the X chromosome can be passed from one generation to the ...
    https://medlineplus.gov/genetics/condition/turner-syndrome - Genetics
  3. 3p deletion syndrome 
    ... Genetic Testing Registry: 3p- syndrome Distal monosomy 3p Partial deletion of the short arm of chromosome 3 National Organization for Rare Disorders (NORD) CHROMOSOME ...
    https://medlineplus.gov/genetics/condition/3p-deletion-syndrome - Genetics
  4. Smith-Magenis syndrome 
    ... called germline mosaicism. 17p- syndrome 17p11.2 monosomy Chromosome 17p deletion syndrome Deletion 17p syndrome Partial monosomy 17p SMS Genetic Testing Registry: Smith-Magenis ...
    https://medlineplus.gov/genetics/condition/smith-magenis-syndrome - Genetics
  5. Dandy-Walker malformation 
    ... people with trisomy 13, trisomy 21, or trisomy 9. This condition can also be associated with missing (deletions) or copied (duplications) pieces of certain chromosomes. Dandy-Walker malformation can also be a feature ...
    https://medlineplus.gov/genetics/condition/dandy-walker-malformation - Genetics
  6. WAGR syndrome 
    ... generation. A child may inherit a copy of chromosome 11 this is missing a piece of the short arm, which causes WAGR syndrome. 11p deletion syndrome 11p partial monosomy syndrome WAGR complex WAGR contiguous gene syndrome ...
    https://medlineplus.gov/genetics/condition/wagr-syndrome - Genetics
  7. Jacobsen syndrome 
    ... 11 and have extra genetic material from another chromosome. These chromosomal changes result in the health problems that are ... Jacobsen syndrome National Organization for Rare ...
    https://medlineplus.gov/genetics/condition/jacobsen-syndrome - Genetics
  8. 16p11.2 deletion syndrome 
    ... genes contribute to the features of 16p11.2 deletion syndrome. chromosome 16 16p11.2 deletion syndrome is considered to ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov CHROMOSOME 16p11.2 DELETION SYNDROME, 593-KB PubMed Bijlsma EK, Gijsbers AC, ...
    https://medlineplus.gov/genetics/condition/16p112-deletion-syndrome - Genetics
  9. Ring chromosome 20 syndrome 
    ... most affected individuals do not have these gene deletions. In these people, the ring chromosome may change the activity of certain genes on ... C. Early pattern of epilepsy in the ring chromosome 20 syndrome. Epilepsia. 2006 Mar;47(3):543-9. doi: 10.1111/j.1528-1167.2006.00465. ...
    https://medlineplus.gov/.../condition/ring-chromosome-20-syndrome - Genetics
  10. Recombinant 8 syndrome 
    ... 8 syndrome is caused by a rearrangement of chromosome 8 that results in a deletion of a piece of the short (p) arm ... a piece of the long (q) arm. The deletion and duplication result in the recombinant 8 chromosome. On the recombinant 8 chromosome, there is one ...
    https://medlineplus.gov/genetics/condition/recombinant-8-syndrome - Genetics
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