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Anita E Beck

Showing results (1-10 of 38) with videos related to

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American Journal of Medical Genetics. Part A|April 1, 2005
Autosomal dominant microtia and ocular coloboma: new syndrome or an extension of the oculo-auriculo-vertebral spectrum?Anita E Beck, Louanne Hudgins, H Eugene Hoyme
Molecular Genetics and Metabolism|March 21, 2006
Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant loadGregory M Enns, Ren-Kui Bai, Anita E Beck, et al.
Pediatric Endocrinology Reviews : PER|May 13, 2015
Obesity management in Prader-Willi syndromeParisa Salehi, Anne Leavitt, Anita E Beck, et al.
Human Molecular Genetics|March 6, 2015
The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscleAlice W Racca, Anita E Beck, Margaret J McMillin, et al.
Cytogenetic and Genome Research|March 9, 2026
The Spectrum of Mosaic Double Aneuploidy of Monosomy X and Trisomy 18: Two New Cases and Review of the LiteratureTeresa M Campbell, Candace T Myers, Cate R Paschal, et al.
Medicine|February 3, 2018
Silent aspiration in infants with Prader-Willi syndrome identified by videofluoroscopic swallow studyParisa Salehi, Holly J Stafford, Robin P Glass, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Methotrexate/misoprostol embryopathy: report of four cases resulting from failed medical abortionMargaret P Adam, Melanie A Manning, Anita E Beck, et al.
American Journal of Medical Genetics. Part A|September 27, 2014
Genotype-phenotype relationships in Freeman-Sheldon syndromeAnita E Beck, Margaret J McMillin, Heidi I S Gildersleeve, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to familiesFernanda Delgado, Holly K Tabor, Penny M Chow, et al.
Frontiers in Pediatrics|November 19, 2025
Case Report: An atypical case of ARPKD highlights the utility and challenges of implementing genetic testing in cystic kidney diseaseJonathan Marquez, Lauren M Hawkins, Anita E Beck, et al.
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics. Part A|April 1, 2005
Autosomal dominant microtia and ocular coloboma: new syndrome or an extension of the oculo-auriculo-vertebral spectrum?Anita E Beck, Louanne Hudgins, H Eugene Hoyme
Molecular Genetics and Metabolism|March 21, 2006
Molecular-clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant loadGregory M Enns, Ren-Kui Bai, Anita E Beck, et al.
Pediatric Endocrinology Reviews : PER|May 13, 2015
Obesity management in Prader-Willi syndromeParisa Salehi, Anne Leavitt, Anita E Beck, et al.
Human Molecular Genetics|March 6, 2015
The embryonic myosin R672C mutation that underlies Freeman-Sheldon syndrome impairs cross-bridge detachment and cycling in adult skeletal muscleAlice W Racca, Anita E Beck, Margaret J McMillin, et al.
Cytogenetic and Genome Research|March 9, 2026
The Spectrum of Mosaic Double Aneuploidy of Monosomy X and Trisomy 18: Two New Cases and Review of the LiteratureTeresa M Campbell, Candace T Myers, Cate R Paschal, et al.
Medicine|February 3, 2018
Silent aspiration in infants with Prader-Willi syndrome identified by videofluoroscopic swallow studyParisa Salehi, Holly J Stafford, Robin P Glass, et al.
American Journal of Medical Genetics. Part A|October 14, 2003
Methotrexate/misoprostol embryopathy: report of four cases resulting from failed medical abortionMargaret P Adam, Melanie A Manning, Anita E Beck, et al.
American Journal of Medical Genetics. Part A|September 27, 2014
Genotype-phenotype relationships in Freeman-Sheldon syndromeAnita E Beck, Margaret J McMillin, Heidi I S Gildersleeve, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to familiesFernanda Delgado, Holly K Tabor, Penny M Chow, et al.
Frontiers in Pediatrics|November 19, 2025
Case Report: An atypical case of ARPKD highlights the utility and challenges of implementing genetic testing in cystic kidney diseaseJonathan Marquez, Lauren M Hawkins, Anita E Beck, et al.
Pageof 4