Publications by authors named "Yonit A Addissie"

15Publications

Identifying environmental risk factors and gene-environment interactions in holoprosencephaly.

Birth Defects Res 2020 Oct 28. Epub 2020 Oct 28.

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/bdr2.1834DOI Listing
October 2020

Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study.

Environ Health 2020 06 8;19(1):65. Epub 2020 Jun 8.

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1186/s12940-020-00611-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7278164PMC
June 2020

Circle of Willis anomalies in Turner syndrome: Absent A1 segment of the anterior cerebral artery.

Birth Defects Res 2019 11 18;111(19):1584-1588. Epub 2019 Oct 18.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/bdr2.1609DOI Listing
November 2019

Tuberous sclerosis in a patient from Nigeria.

Am J Med Genet A 2019 08 29;179(8):1423-1425. Epub 2019 May 29.

Center for Research on Genomics and Global Health, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.61194DOI Listing
August 2019

Williams-Beuren syndrome in diverse populations.

Am J Med Genet A 2018 05;176(5):1128-1136

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

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http://doi.wiley.com/10.1002/ajmg.a.38672
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http://dx.doi.org/10.1002/ajmg.a.38672DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007881PMC
May 2018

Muenke syndrome: An international multicenter natural history study.

Am J Med Genet A 2016 Apr 6;170A(4):918-29. Epub 2016 Jan 6.

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.37528DOI Listing
April 2016

Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature.

Am J Med Genet A 2015 Nov 6;167A(11):2657-63. Epub 2015 Aug 6.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.37259DOI Listing
November 2015