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Results 1 - 10 of 20 for Clinical
  1. Chromosome 18 
    ... dosage map of Chromosome 18: a map with clinical utility. Genet Med. 2009 Nov;11(11):778- ... Lonnqvist T, Valanne L, Pihko H. 18q deletions: clinical, molecular, and brain MRI findings of 14 individuals. ...
    https://medlineplus.gov/genetics/chromosome/18 - Genetics
  2. Chromosome 5 
    ... RJ, Gutierrez NC, Hernandez-Rivas JM. Incidence and clinical characteristics of myeloproliferative neoplasms displaying a PDGFRB rearrangement. ... chat syndrome: genotype-phenotype correlations and recommendations for clinical management. Dev Med Child Neurol. 2002 Jul;44( ...
    https://medlineplus.gov/genetics/chromosome/5 - Genetics
  3. Chromosome 15 
    ... Central Bittel DC, Butler MG. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology. Expert Rev Mol ... Micheli R, Gagliardi C, Balottin U. Relationship between clinical and genetic features in "inverted duplicated chromosome 15" ...
    https://medlineplus.gov/genetics/chromosome/15 - Genetics
  4. Chromosome 3 
    ... Zackai EH, Bejjani BA, Shaffer LG. Expanding the clinical phenotype of the 3q29 microdeletion syndrome and characterization ... Szuhai K, Wintle RF, Scherer SW. Molecular and clinical characterization of de novo and familial cases with ...
    https://medlineplus.gov/genetics/chromosome/3 - Genetics
  5. Mitochondrial DNA 
    ... Wong LJ. Sequence homology at the breakpoint and clinical phenotype of mitochondrial DNA deletion syndromes. PLoS One. ... Tondi M, Muntoni F, Zeviani M, Mastropaolo C. Clinical and EEG findings in eleven patients affected by ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  6. Chromosome 2 
    ... 2 Falk RE, Casas KA. Chromosome 2q37 deletion: clinical and molecular aspects. Am J Med Genet C ... The 2q37-deletion syndrome: an update of the clinical spectrum including overweight, brachydactyly and behavioural features in ...
    https://medlineplus.gov/genetics/chromosome/2 - Genetics
  7. Chromosome 16 
    ... Molecular characterization of partial trisomy 16q24.1-qter: clinical report and review of the literature. Am J ... Yong PJ, Barrett IJ, Kalousek DK, Robinson WP. Clinical aspects, prenatal diagnosis, and pathogenesis of trisomy 16 ...
    https://medlineplus.gov/genetics/chromosome/16 - Genetics
  8. X chromosome 
    ... S, Lin-Su K, McElreavey K, New MI. Clinical, hormonal and cytogenetic evaluation of 46,XX males ... chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects ( ...
    https://medlineplus.gov/genetics/chromosome/x - Genetics
  9. Chromosome 1 
    ... B. Genetic aberrations including chromosome 1 abnormalities and clinical features of plasma cell leukemia. Leuk Res. 2009 ... 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome. Am J Hum Genet. ...
    https://medlineplus.gov/genetics/chromosome/1 - Genetics
  10. Chromosome 11 
    ... J, Luis CA, Sika M. WAGR syndrome: a clinical review of 54 cases. Pediatrics. 2005 Oct;116( ... 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects. Eur J Hum Genet. 2004 ...
    https://medlineplus.gov/genetics/chromosome/11 - Genetics
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