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Results 1 - 10 of 19 for De
  1. ... a microdeletion) on chromosome 17 can cause Koolen-de Vries syndrome. This disorder is characterized by developmental ... variety of physical abnormalities.Most people with Koolen-de Vries syndrome are missing a sequence of about ...
  2. ... 10.1038/sj.leu.2402718. Citation on PubMed de The H, Lavau C, Marchio A, Chomienne C, ... Skinner C, Stevenson RE, Schroer RJ, Novara F, De Gregori M, Ciccone R, Broomer A, Casuga I, ...
  3. ... FT, Nogueira SI, Christofolini DM, Smith Mde A, de Mello CB, Brunoni D, Melaragno MI. Pure duplication ... Baralle D, Collins A, Mercer C, Norga K, de Ravel T, Devriendt K, Bongers EM, de Leeuw ...
  4. ... M, Le Merrer M, Raoul O, Prieur M, de Blois MC, Philippe A, Vekemans M, Romana SP. ... Pyatt RE, Waggoner DJ, Shaffer LG, Lin AE, de Vries BB, Mendoza-Londono R, Elsea SH. Reciprocal ...
  5. ... 0103. Epub 2011 Feb 24. Citation on PubMed De Braekeleer E, Douet-Guilbert N, Rowe D, Bown N, Morel F, Berthou C, Ferec C, De Braekeleer M. ABL1 fusion genes in hematological malignancies: ...
  6. ... JD, Carter EM, Sebold C, Heard PL, Hale DE. A gene dosage map of Chromosome 18: a ... J, Hasi M, Hill A, Pankratz L, Hale DE, Cody JD. Tetrasomy 18p: report of the molecular ...
  7. ... Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, ... Ouweland JM, Lemkes HH, Ruitenbeek W, Sandkuijl LA, de Vijlder MF, Struyvenberg PA, van de Kamp JJ, ...
  8. ... L, Lopez-Corral L, Megido M, Giraldo P, de las Heras N, Vanegas RJ, Gutierrez NC, Hernandez- ... D. Whole exome sequencing in family trios reveals de novo mutations in PURA as a cause of ...
  9. ... D, Schrander-Stumpel C, Stegmann AP, Frints SG, de Vries BB, Ceulemans B, Kooy RF. Fourteen new ... Jalal SM, Kukolich MK, Lockhart LH, Tonk VS. De novo supernumerary ring chromosome 7: first report of ...
  10. ... Statistics Van Limbergen H, Poppe B, Janssens A, De Bock R, De Paepe A, Noens L, Speleman F. Molecular cytogenetic ...
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