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Cell-free DNA screening positive for monosomy X: clinical evaluation and management of suspected maternal or fetal Turner syndrome.
Dowlut-McElroy, Tazim; Davis, Shanlee; Howell, Susan; Gutmark-Little, Iris; Bamba, Vaneeta; Prakash, Siddharth; Patel, Sheetal; Fadoju, Doris; Vijayakanthi, Nandini; Haag, Mary; Hennerich, Deborrah; Dugoff, Lorraine; Shankar, Roopa Kanakatti.
Afiliación
  • Dowlut-McElroy T; Pediatric and Adolescent Gynecology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD; Department of Surgery, Children's National Hospital, Washington, DC. Electronic address: tazim.dowlut-mcelroy@nih.gov.
  • Davis S; eXtraOrdinarY Kids Turner Syndrome Clinic, Children's Hospital Colorado, Aurora, CO; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO.
  • Howell S; eXtraOrdinarY Kids Turner Syndrome Clinic, Children's Hospital Colorado, Aurora, CO; Department of Pediatrics, University of Colorado School of Medicine, Aurora, CO.
  • Gutmark-Little I; Division of Endocrinology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
  • Bamba V; Division of Endocrinology, Children's Hospital of Philadelphia, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Prakash S; Department of Internal Medicine, McGovern Medical School, The University of Texas Health Science Center at Houston, Houston, TX.
  • Patel S; Division of Pediatric Cardiology, Ann & Robert H. Lurie Children's Hospital of Chicago, Northwestern University Feinberg School of Medicine, Chicago, IL.
  • Fadoju D; Division of Pediatric Endocrinology, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA.
  • Vijayakanthi N; Division of Pediatric Endocrinology, Emory University School of Medicine, Children's Healthcare of Atlanta, Atlanta, GA.
  • Haag M; Colorado Genetics Laboratory, Department of Pathology, University of Colorado School of Medicine, Aurora, CO.
  • Hennerich D; Colorado Genetics Laboratory, Department of Pathology, University of Colorado School of Medicine, Aurora, CO.
  • Dugoff L; Divisions of Reproductive Genetics and Maternal Fetal Medicine, Department of Obstetrics and Gynecology, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
  • Shankar RK; Division of Endocrinology, Children's National Hospital, George Washington University School of Medicine and Health Sciences, Washington, DC.
Am J Obstet Gynecol ; 227(6): 862-870, 2022 12.
Article en En | MEDLINE | ID: mdl-35841934
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Turner / Trastornos de los Cromosomas / Ácidos Nucleicos Libres de Células Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Am J Obstet Gynecol Año: 2022 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndrome de Turner / Trastornos de los Cromosomas / Ácidos Nucleicos Libres de Células Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies / Screening_studies Límite: Female / Humans / Pregnancy Idioma: En Revista: Am J Obstet Gynecol Año: 2022 Tipo del documento: Article