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A-Z Articles Index by First Author's Last Name

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D'Angelo CS et al. Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems. Eur J Med Genet. 2006 November - December;49(6):451-460. Epub 2006 Mar 10.

Da Lee R et al. Differential gene profiles in developing embryo and fetus after in utero exposure to ethanol. J Toxicol Environ Health A. 2004 Dec;67(23-24):2073-84.

Dao MA & Nolta JA Immunodeficient mice as models of human hematopoietic stem cell engraftment. Curr Opin Immunol. 1999 Oct;11(5):532-7.

Darnell JC et al. Fragile X Mental Retardation Protein Targets G Quartet mRNAs Important for Neuronal Function. Cell. 2001 Nov 16;107(4):489-99.

DeBaun MR et al. Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19. Am J Hum Genet. 2002 Nov 18;72(1). [epub ahead of print]

de Gregori M et al. Crytptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients. J Med Genet. 2007 Dec;44(12):750-62. Epub 2007 Aug 31
DeKosky ST and Marek K. Looking backward to move forward: early detection of neurodegenerative disorders. Science. 2003 Oct 31;302(5646):830-4.

de Lonlay P et al. Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. J Clin Invest. 1997 Aug 15;100(4):802-7.

De Sandre-Giovannoli A et al. Lamin a truncation in Hutchinson-Gilford progeria. Science. 2003 Jun 27;300(5628):2055.

de Vries BB et al. Diagnostic genome profiling in mental retardation. Am J Hum Genet. 2005 Oct;77(4):606-16. Epub 2005 Aug 30.

Del Campo M et al. (1999) Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster. Am J Hum Genet  65:104-110.

Del Castillo I et al. Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study. Am J Hum Genet. 2003 Dec;73(6):1452-8. Epub 2003 Oct 21.

Del Castillo I et al. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment. N Engl J Med. 2002 Jan 24;346(4):243-9.

Dernburg AF et al. A chromosome RNAissance. Cell. 2002 Oct 18;111(2):159-62.

Devoss J, et al. Spontaneous autoimmunity prevented by thymic expression of a single self-antigen. J Exp Med. 2006 Nov 27;203(12):2727-35. Epub 2006 Nov 20.
Diabetes Genetics Initiative of Broad Institute of Harvard and MIT, Lund University, and Novartis Institutes of BioMedical Research, et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science. 2007 Jun 1;316(5829):1331-6. Epub 2007 Apr 26.

Digilio MC, et al. Grouping of Multiple-Lentigines/LEOPARD and Noonan Syndromes on the PTPN11 gene. Am J Hum Genet. 2002; 71(2).

Djuric U, et al. Familial molar tissues due to mutations in the inflammatory gene, NALP7, have normal postzygotic DNA methylation. Hum Genet. 2006 Oct;120(3):390-5. Epub 2006 Jul 28.
Dlugosz A & Talpaz M (2009). Following the Hedgehog to New Cancer Therapies New England Journal of Medicine, 361 (12), 1202-1205.

Dode C, et al. Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome. Nat Genet. 2003 Apr;33(4): 463-5. Epub 2003 Mar 10.

Dölen G et al. Correction of Fragile X Syndrome in Mice. Neuron. 2007 Dec 20;56(6):955-962.

Doolin MT et al. Maternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifida. Am J Hum Genet. 2002;71(5):1222-6.

Douglas J et al. NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypes. Am J Hum Genet. 2003; 72:132-143.
Du H et al. Cyclophilin D deficiency attenuates mitochondrial and neuronal perturbation and ameliorates learning and memory in Alzheimer's disease. Nat Med. 2008 Oct;14(10):1097-105. Epub 2008 Sep 21.

Duffy DL et al. Interactive effects of MC1R and OCA2 on melanoma risk phenotypes. Hum Mol Genet. 2004 Feb 15;13(4):447-61. Epub 2004 Jan