Chad Haldeman-Englert

Chad Haldeman-Englert

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Chad Haldeman-Englert

Chad Haldeman-Englert

Publications by authors named "Chad Haldeman-Englert"

Are you Chad Haldeman-Englert?   Register this Author

19Publications

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Fetus in Fetu in Lieu of a Sacrococcygeal Teratoma: A Case Illuminating the Utility of Serial Prenatal Sonographic Examinations in Diagnosis.

J Ultrasound Med 2017 Feb 27;36(2):453-455. Epub 2016 Dec 27.

Department of Pediatrics, Section on Medical Genetics, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.

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http://dx.doi.org/10.7863/ultra.16.02040DOI Listing
February 2017

Narrowing the critical region for congenital vertical talus in patients with interstitial 18q deletions.

Am J Med Genet A 2013 May 13;161A(5):1117-21. Epub 2013 Mar 13.

Department of Medical Genetics, Spectrum Health, Grand Rapids, MI 49503, USA.

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http://dx.doi.org/10.1002/ajmg.a.35791DOI Listing
May 2013

Spectrum of elastin sequence variants and cardiovascular phenotypes in 49 patients with Williams-Beuren syndrome.

Am J Med Genet A 2013 Mar 7;161A(3):527-33. Epub 2013 Feb 7.

Department of Genetics, Albert Einstein College of Medicine, Bronx, New York 10461, USA.

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http://dx.doi.org/10.1002/ajmg.a.35784DOI Listing
March 2013

Duplication 12p and Pallister-Killian syndrome: a case report and review of the literature toward defining a Pallister-Killian syndrome minimal critical region.

Am J Med Genet A 2012 Dec 20;158A(12):3033-45. Epub 2012 Nov 20.

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.

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http://dx.doi.org/10.1002/ajmg.a.35500DOI Listing
December 2012

Loeys-Dietz syndrome presenting as respiratory distress due to pulmonary artery dilation.

Am J Med Genet A 2012 May 9;158A(5):1212-5. Epub 2012 Apr 9.

Wake Forest School of Medicine, Winston-Salem, North Carolina 27157, USA.

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http://dx.doi.org/10.1002/ajmg.a.35274DOI Listing
May 2012

Revision of "A 223-kb de novo deletion of PAX9 in a patient with oligodontia".

J Craniofac Surg 2012 Mar;23(2):e149-51

Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania 19104, USA.

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https://insights.ovid.com/crossref?an=00001665-201203000-001
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http://dx.doi.org/10.1097/SCS.0b013e31824cdcddDOI Listing
March 2012

Genes and biological processes commonly disrupted in rare and heterogeneous developmental delay syndromes.

Hum Mol Genet 2011 Mar 8;20(5):880-93. Epub 2010 Dec 8.

Division of Human Genetics, The Children’s Hospital of Philadelphia, Philadelphia, PA, USA.

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http://dx.doi.org/10.1093/hmg/ddq527DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3033180PMC
March 2011

A 223-kb de novo deletion of PAX9 in a patient with oligodontia.

J Craniofac Surg 2010 May;21(3):837-9

Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.

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https://insights.ovid.com/crossref?an=00001665-201005000-000
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http://dx.doi.org/10.1097/SCS.0b013e3181d87912DOI Listing
May 2010

A 3.1-Mb microdeletion of 3p21.31 associated with cortical blindness, cleft lip, CNS abnormalities, and developmental delay.

Eur J Med Genet 2009 Jul-Aug;52(4):265-8. Epub 2008 Dec 13.

Division of Human Genetics, Bioinformatics Core, Center for Applied Genomics, Children's Hospital of Philadelphia, and Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.

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http://linkinghub.elsevier.com/retrieve/pii/S176972120800165
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http://dx.doi.org/10.1016/j.ejmg.2008.11.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4391973PMC
November 2009