NatalieGBlagowidowMD

PubMed

• Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.
  Anne S Bassett, Erik Boot, Bruno Marino, Julie S Moldenhauer, Sólveig Óskarsdóttir, Carolina Putotto, Erica Schindewolf, Donna M McDonald-McGinn, Elizabeth Goldmuntz, ...> ;Prenatal Diagnosis. 2024 Apr 9
• 13 citations
  Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions.
  Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C Y Lo...> ;Genes. 2023 Jan 6
• 2 citations
  Obstetrics and gynecology in Ehlers-Danlos syndrome: A brief review and update.
  Natalie Blagowidow> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2021 Nov 12
• 178 citations
  Diagnosis and management of Cornelia de Lange syndrome: first international consensus statement
  Antonie D. Kline, Joanna Moss, Angelo Selicorni, Anne Marie Bisgaard, Matthew A. Deardorff, Peter M. Gillett, Stacey L. Ishman, Lynne M. Kerr, Alex V. Levin, Paul A. M...> ;Nature Reviews. Genetics. 2018 Oct 1
• 4 citations
  Clinical, developmental and molecular update on Cornelia de Lange syndrome and the cohesin complex: abstracts from the 2014 Scientific and Educational Symposium.
  Antonie D. Kline, Anne L. Calof, Arthur D. Lander, Jennifer L. Gerton, Ian D. Krantz, Dale Dorsett, Matthew A. Deardorff, Natalie Blagowidow, Kyoko Yokomori, Katsuhiko...> ;American Journal of Medical Genetics. Part A. 2015 Jun 1
• 14 citations
  Cornelia de Lange syndrome: extending the physical and psychological phenotype.
  Chris Oliver, Maria Francesca Bedeschi, Natalie Blagowidow, Cheri S. Carrico, Anna Cereda, David R. FitzPatrick, Cristina Gervasini, Gemma M. Griffith, Antonie D. Klin...> ;American Journal of Medical Genetics. Part A. 2010 May 1
• 109 citations
  Natural history of aging in Cornelia de Lange syndrome
  Antonie D. Kline, Marco A. Grados, Paul D. Sponseller, Howard P. Levy, Natalie Blagowidow, Christianne Schoedel, Joni Rampolla, Douglas K. Clemens, Ian D. Krantz, Amy ...> ;American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 2007 Aug 15
• 17 citations
  Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprinting.
  Jeffrey E. Ming, Natalie Blagowidow, Joan H.M. Knoll, Lori Rollings, Paolo Fortina, Donna M. McDonald-McGinn, Nancy B. Spinner, Elaine H. Zackai> ;American Journal of Medical Genetics. 2000 May 1
• 17 citations
  Ullrich‐Turner syndrome in an XY female fetus with deletion of the sex‐determining portion of the Y chromosome
  Natalie Blagowidow, David C. Page, Dale Huff, Michael T. Mennuti> ;American Journal of Medical Genetics. 1989 Oct 1
• 60 citations
  XY gonadal dysgenesis: genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis.
  Joe Leigh Simpson, Natalie Blagowidow, Alice O. Martin> ;Human Genetics. 1981 Jan 1
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Journal Articles

• Diagnosis and Management of Cornelia De Lange Syndrome: First International Consensus Statement  
  Marco Grados, Antonie D Kline, Matthew A Deardorff, Natalie Blagowidow, Stacey L Ishman, Alex V Levin, Nature