Publications by authors named "John A Bernat"

13Publications

Interstitial lung disease of infancy caused by a new mutation.

Clin Case Rep 2017 06 4;5(6):739-743. Epub 2017 Apr 4.

Department of Pediatrics and Communicable Diseases University of Michigan Medical School Ann Arbor Michigan USA.

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http://dx.doi.org/10.1002/ccr3.901DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5458033PMC
June 2017

Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.

Am J Med Genet A 2015 Nov 31;167A(11):2664-73. Epub 2015 Jul 31.

Department of Human Genetics, Emory University School of Medicine, Atlanta, Georgia.

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http://dx.doi.org/10.1002/ajmg.a.37269DOI Listing
November 2015

Breast fibroadenomas in the pediatric population: common and uncommon sonographic findings.

Pediatr Radiol 2010 Oct 7;40(10):1681-9. Epub 2010 May 7.

Section of Pediatric Radiology, Department of Radiology, C. S. Mott Children's Hospital, University of Michigan Health System, 1500 E. Medical Center Drive, Ann Arbor, MI 48109-5252, USA.

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http://dx.doi.org/10.1007/s00247-010-1678-7DOI Listing
October 2010

Distant conserved sequences flanking endothelial-specific promoters contain tissue-specific DNase-hypersensitive sites and over-represented motifs.

Hum Mol Genet 2006 Jul 24;15(13):2098-105. Epub 2006 May 24.

Department of Human Genetics, Howard Hughes Medical Institute, USA.

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http://dx.doi.org/10.1093/hmg/ddl133DOI Listing
July 2006

Heterochromatin protein 2 (HP2), a partner of HP1 in Drosophila heterochromatin.

Proc Natl Acad Sci U S A 2002 Oct 10;99(22):14332-7. Epub 2002 Oct 10.

Department of Biology, Washington University, CB-1229, St. Louis, MO 63130, USA.

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http://dx.doi.org/10.1073/pnas.212458899DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC137884PMC
October 2002