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Results 1 - 10 of 15 for news
  1. ... mapping with further characterization of the phenotype, a new cohort of 86 patients. Am J Med Genet ... proximal 1p36 deletions using array-CGH: a possible new syndrome. Clin Genet. 2007 Oct;72(4):329- ...
  2. ... RE. Chromosome 2q terminal deletion: report of 6 new patients and review of phenotype-breakpoint correlations in ... including overweight, brachydactyly and behavioural features in 14 new patients. Eur J Hum Genet. 2013 Jun;21( ...
  3. ... G, Santorelli FM, Cotrufo R. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF ... DN, Debono AG, Morgan-Hughes JA, Hanna MG. New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) ...
  4. ... Anneren G. Trisomy 4q syndrome: presentation of a new case and review of the literature. Ann Genet. ... currently accepted WHS critical region and defining a new critical region, WHSCR-2. Am J Hum Genet. ...
  5. ... S, Tansil S, Lin-Su K, McElreavey K, New MI. Clinical, hormonal and cytogenetic evaluation of 46, ... J, Visootsak J, Hansen R, Hagerman R. A new look at XXYY syndrome: medical and psychological features. ...
  6. ... Thomas GH, Batista DA. 3q29 interstitial microduplication: a new syndrome in a three-generation family. Am J ...
  7. ... A, Sakata S, Ohno K, Yamamoto T. A new microdeletion syndrome of 5q31.3 characterized by severe ...
  8. ... cohort of 13 patients with transient neonatal diabetes: new hypothesis raised by the finding of a unique ...
  9. ... de Vries BB, Ceulemans B, Kooy RF. Fourteen new cases contribute to the characterization of the 7q11. ...
  10. ... Y, Luo Y. Chromosome 10q26 deletion syndrome: Two new cases and a review of the literature. Mol ...
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