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Patterns of congenital anomalies among individuals with trisomy 13 in Texas.
Diaz, Diego; Benjamin, Renata H; Navarro Sanchez, Maria Luisa; Mitchell, Laura E; Langlois, Peter H; Canfield, Mark A; Chen, Han; Scheuerle, Angela E; Schaaf, Christian P; Scott, Daryl A; Northrup, Hope; Ray, Joseph W; McLean, Scott D; Swartz, Michael D; Ludorf, Katherine L; Lupo, Philip J; Agopian, A J.
Afiliación
  • Diaz D; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
  • Benjamin RH; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
  • Navarro Sanchez ML; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
  • Mitchell LE; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
  • Langlois PH; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA.
  • Canfield MA; Birth Defects Epidemiology and Surveillance Branch, Texas Department of State Health Services, Austin, Texas, USA.
  • Chen H; Department of Epidemiology, Human Genetics and Environmental Sciences, UTHealth School of Public Health, Houston, Texas, USA.
  • Scheuerle AE; Center for Precision Health, UTHealth School of Public Health and UTHealth School of Biomedical Informatics, Houston, Texas, USA.
  • Schaaf CP; Department of Pediatrics, Division of Genetics and Metabolism, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
  • Scott DA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Northrup H; Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, Texas, USA.
  • Ray JW; Institute of Human Genetics, Heidelberg University, Heidelberg, Germany.
  • McLean SD; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, USA.
  • Swartz MD; Department of Molecular Physiology and Biophysics, Baylor College of Medicine, Houston, Texas, USA.
  • Ludorf KL; Department of Pediatrics, Division of Medical Genetics, McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.
  • Lupo PJ; Department of Pediatrics, Division of Medical Genetics and Metabolism, University of Texas Medical Branch, Galveston, Texas, USA.
  • Agopian AJ; Clinical Genetics Section, The Children's Hospital of San Antonio, San Antonio, Texas, USA.
Am J Med Genet A ; 185(6): 1787-1793, 2021 06.
Article en En | MEDLINE | ID: mdl-33749998
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Holoprosencefalia / Síndrome de la Trisomía 13 / Cardiopatías Congénitas Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn / Pregnancy País/Región como asunto: America do norte Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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XML
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Anomalías Múltiples / Holoprosencefalia / Síndrome de la Trisomía 13 / Cardiopatías Congénitas Límite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn / Pregnancy País/Región como asunto: America do norte Idioma: En Revista: Am J Med Genet A Asunto de la revista: GENETICA MEDICA Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos