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Results 1 - 10 of 25 for Three M syndrome 1
  1. Chromosome 3 
    ... 3q29 interstitial microduplication: a new syndrome in a three-generation family. Am J ... detailed molecular cytogenetic and clinical characterization of three ...
    https://medlineplus.gov/genetics/chromosome/3 - Genetics
  2. Chromosome 7 
    ... J Med Genet A. 2003 Dec 15;123A(3):236-42. doi: 10.1002/ajmg.a.20318. Citation on PubMed Kozel BA, Barak B, Kim CA, Mervis CB, Osborne LR, Porter M, Pober BR. Williams syndrome. Nat Rev Dis Primers. 2021 Jun 17;7(1):42. doi: 10.1038/s41572-021-00276-z. ...
    https://medlineplus.gov/genetics/chromosome/7 - Genetics
  3. Chromosome 21 
    ... C Semin Med Genet. 2006 Aug 15;142C(3):196-205. doi: 10.1002/ajmg.c.30098. Citation on PubMed or Free article on PubMed Central Gardiner K, Davisson M. The sequence of human chromosome 21 and implications for research into Down syndrome. Genome Biol. 2000;1(2):REVIEWS0002. doi: 10.1186/gb-2000-1- ...
    https://medlineplus.gov/genetics/chromosome/21 - Genetics
  4. Chromosome 20 
    ... phenotype. Am J Med Genet A. 2005 Sep 1;137A(3):308-12. doi: 10.1002/ajmg.a.30877. ... epilepticus. A new epileptic syndrome. Brain. 1997 Jun;120 ( Pt 6):939-53. ...
    https://medlineplus.gov/genetics/chromosome/20 - Genetics
  5. Chromosome 9 
    ... Genome Browser: Statistics Willemsen MH, Beunders G, Callaghan M, de ... microdeletions. Clin Genet. 2011 Jul;80(1):31-8. doi: 10.1111/j.1399-0004. ...
    https://medlineplus.gov/genetics/chromosome/9 - Genetics
  6. Chromosome 16 
    ... a new contiguous gene syndrome, the chromosome 16p13.3 deletion syndrome alias ... partial trisomy 16q24.1-qter: clinical report and review of the literature. ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  7. Chromosome 12 
    ... review. Arch Pathol Lab Med. 2007 Jan;131(1):152-6. doi: ... syndrome: extraordinary finding of an analphoid, inverted duplicated marker. ...
    https://medlineplus.gov/genetics/chromosome/12 - Genetics
  8. Chromosome 15 
    ... T. Behavioral differences among subjects with Prader-Willi syndrome and type I or type II deletion and maternal disomy. Pediatrics. 2004 Mar;113(3 Pt 1):565-73. doi: 10.1542/peds.113.3. ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  9. Chromosome 2 
    ... Am J Med Genet. 2002 Aug 15;111(3):319-23. doi: 10.1002/ajmg.10537. Citation on PubMed Heller M, Provan D, Amess JA, Dixon-McIver A. Myelodysplastic syndrome associated with trisomy 2. Clin Lab Haematol. 2005 ...
    https://medlineplus.gov/genetics/chromosome/2 - Genetics
  10. Chromosome 4 
    ... ST, Hannes F, Fisch GS, Vermeesch JR, Zollino M. Pathogenic significance of deletions distal to the currently described Wolf-Hirschhorn syndrome critical regions on 4p16.3. Am J Med Genet C Semin Med Genet. ...
    https://medlineplus.gov/genetics/chromosome/4 - Genetics
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