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32199 publications found in the database

*2012 (1980)

*Starting in 2010, coverage has been refocused on core journals.

2012 Publications

Compensatory dendritic cell development mediated by BATF-IRF interactions
Tussiwand, R. et al. Nature 490(7421), NPG, 2012  PubMed

Computational identification of transcriptionally co-regulated genes, validation with the four ANT isoform genes
Dupont, P. Y. et al. BMC Genomics 13(), NPG, 2012, Human Genome U133 Plus 2.0 Array  PubMed

Familial 25.3 Mb Inverted Duplication of Bands q32.1 to q35.1 on Chromosome 4 With Psychomotor Impairments
Martin, J. et al. American Journal of Medical Genetics Part a 158A(10), 2624-8, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Interstitial 3p25.3-p26.1 Deletion in a Patient With Intellectual Disability
Riess, A. et al. American Journal of Medical Genetics Part a 158A(10), 2587-90, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Life-History Chronicle for a Patient With the Recently Described Chromosome 4q21 Microdeletion Syndrome
Tsang, E. et al. American Journal of Medical Genetics Part a 158A(10), 2606-9, 2012  PubMed

Macrocephaly, Obesity, Mental (Intellectual) Disability, and Ocular Abnormalities: Alternative Definition and Further Delineation of MOMO Syndrome
Di Donato, N. et al. American Journal of Medical Genetics Part a 158A(11), 2857-62, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Insertional Translocation of 15q25-q26 into 11p13 and Duplication at 8p23.1 Characterized by High Resolution Arrays in a Boy With Congenital Malformations and Aniridia
Simioni, M. et al. American Journal of Medical Genetics Part a 158A(11), 2905-10, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Re-assigned Diagnosis of D4ST1-Deficient Ehlers-Danlos Syndrome (Adducted Thumb-Clubfoot Syndrome) After Initial Diagnosis of Marden-Walker Syndrome
Winters, K. A. et al. American Journal of Medical Genetics Part a 158A(11), 2935-40, 2012, Genome-Wide Human SNP Array 6.0  PubMed

BPES With Atypical Premature Ovarian Insufficiency, and Evidence of Mitotic Recombination, in a Woman With Trisomy X and a Translocation t(3; 11)(q22.3;q14.1)
Schlade-Bartusiak, K. et al. American Journal of Medical Genetics Part a 158A(9), 2322-7, 2012, Genome-Wide Human SNP Array 6.0  PubMed

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