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193 results
  1. NLM Digital Collections - Cumulated list of new medical subject headings, 1963-1973 
    Publication: [Bethesda, MD] : U.S. Dept. of Health, Education, and Welfare, Public Health Service, National Institutes of Health, [1973]
    ... POLYPLOIDY SEX CHROMOSOME ABNORMALITIES SEX CHROMATIN CHROMOSOME ABNORMALITIES TRISOMY GENES CHROMOSOME MAPPING KARYOTYPING CHROMATIDS CHROMOSOMES, BACTERIAL CHROMOSOMES, HUMAN, 1-3 CHROMOSOMES, HUMAN, 13-15 CHROMOSOMES, HUMAN, 16-18 CHROMOSOMES, HUMAN, 19-20 CHROMOSOMES, HUMAN, 21-22 ...
  2. ... hCG and PAPP-A MoM in normal and trisomy 21 pregnancies. Prenatal Diagnosis. 2009 ... 2009 Jun; 18 (6):1699–705. Off topic . [ PMC free article : ...
  3. ... high quality according to QUADAS 2 criteria. Table 18 Accuracy data for persons with type 1 diabetes. We found no studies that provided accuracy data on patients with other auto-immune diseases, Turner's syndrome, or Trisomy 21. Although cirrhosis of the liver is not ...
  4. ... 0008; and CIR rate, 3% ± 2% vs. 27% ± 18%, P = .003). Less toxicity was seen in this trial, and treatment-related mortality remained low (2.9% vs. 5%, P = .276). The following two prognostic factors were identified:[ 13 ] Trisomy 8 was an adverse factor (n = 37; OS ...
  5. Trisomy 21; Down's syndrome ... 21. This form of Down syndrome is called trisomy 21. The extra chromosome causes problems with the ... syndrome.html . Updated May 16, 2024. Accessed June 18, 2024. Cooke DW, DiVall SA, Radovick S. Normal and ...
  6. ... derived (fetus has Prader-Willi syndrome [PWS]). If trisomy 15 or mosaic trisomy 15 is detected on CVS, and if subsequent amniocentesis reveals 46 chromosomes, the possibility of trisomy rescue leading to AS (paternal UPD) or PWS ( ...
  7. NLM Digital Collections - MEDLARS training program : indexing training syllabus 
    Publication: [Bethesda, Md.] : National Library of Medicine, Index Section, 1969
    ... yrs.) X CARDIOVASCULAR DISEASES *diaenosis X ADOLESCENCE (13-18 yrs.) RUBELLA *complications X ADULT (19-44 yrs.) ELLIS-VAN CREVELD SYNDROME X MIDDLE AGE (45-64 yrs.) TRISOMY AGED (65- yrs.) LIPOCHONDRODYSTROPHY CATS HYPERCALCEMIA CATTLE DEAFNESS ^ ...
  8. ... and 16.[ 11 ] Gain of whole chromosome 8 (trisomy 8). Trisomy 8 is the most frequent chromosomal alteration in ... in Ewing's sarcoma. II. Nonrandom additional changes, trisomy 8 and der(16)t(1;16). Cancer ...
  9. ... distinctly separate entities [ Zweier et al 2013 ]. Mosaic trisomy 9. An individual with mosaic trisomy 9 had features similar to those of CSS, ... 9. [ PubMed : 3346785 ] Kushnick T, Adessa GM. Partial trisomy 9 with resemblance to Coffin-Siris syndrome. J ...
  10. ... CSF) contribute to the development of MDS.[ 4 ] Trisomy 21 syndrome: GATA1 variants are nearly always present in the transient leukemia associated with Trisomy 21 and MDS in children younger than 3 ...
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