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Results 1 - 10 of 19 for Y chromosome deletions
  1. ... Q, Wu J, Zhang Z, Ji Y, Luo Y. Chromosome 10q26 deletion syndrome: Two new cases and a review of ...
  2. ... the pseudoautosomal regions of the extra X and Y chromosomes likely contribute to the signs and symptoms of 48,XXYY syndrome. More About This Health Condition Deletions of small amounts of genetic material in certain ...
  3. ... AR, Fujiyama A, Hattori M, Birren BW, Sakaki Y, Lander ES. DNA sequence and analysis of ... of 18p deletions: evidence for a breakpoint cluster. Genet Med. 2002 ...
  4. ... cells; other cells have one X and one Y chromosome. In these individuals, the ... A deletion of genetic material in a region of the ...
  5. ... JC, Morales A, Menzie CM, Williams K, Fan YS. Characterization of 11p14-p12 deletion in WAGR ... Citation on PubMed
  6. ... neurological functions such as learning, memory, and behavior.Chromosome 2 deletions or duplications that cause MAND lead to an ... the loss or gain of other genes in chromosome 2 deletions or duplications contribute to the features of MAND. ...
  7. ... Campbell LJ, Bentley DR, Deloukas P, Green AR. Chromosome 20 deletions in myeloid malignancies: reduction of the common deleted ... Krantz ID, Spinner NB. SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variation. Hum Mutat. ...
  8. ... Collins VP. 1p36 is a preferential target of chromosome 1 deletions in astrocytic tumours and homozygously deleted in a ... JL, Tobias ES, Lilley C, Armengol L, Spysschaert Y, Verloo P, De Coene A, Goossens L, Mortier ...
  9. ... located. Many cases of NMIBC tumors have a chromosome 9 deletion, which typically occurs early in tumor formation. These ... Citation on PubMed Stewart DR, Kleefstra T. The chromosome 9q subtelomere deletion syndrome. Am J Med Genet C Semin Med ...
  10. ... Hanna NN, Brooks SS. Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature. Clin Dysmorphol. 2007 Jul;16(3):135-140. doi: 10.1097/MCD.0b013e3281e668d5. Citation on PubMed
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