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Delineation of candidate genes responsible for structural brain abnormalities in patients with terminal deletions of chromosome 6q27.
Peddibhotla, Sirisha; Nagamani, Sandesh C S; Erez, Ayelet; Hunter, Jill V; Holder, J Lloyd; Carlin, Mary E; Bader, Patricia I; Perras, Helene M F; Allanson, Judith E; Newman, Leslie; Simpson, Gayle; Immken, LaDonna; Powell, Erin; Mohanty, Aaron; Kang, Sung-Hae L; Stankiewicz, Pawel; Bacino, Carlos A; Bi, Weimin; Patel, Ankita; Cheung, Sau W.
Afiliación
  • Peddibhotla S; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Nagamani SC; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Erez A; 1] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA [2] Department of Biological Regulation, Weizmann Institute of Science, Rehovot, Israel.
  • Hunter JV; Department of Radiology, Baylor College of Medicine, Houston, TX, USA.
  • Holder JL; 1] Department of Pediatrics, Division of Neurology and Developmental Neuroscience, Baylor College of Medicine, Houston, TX, USA [2] Texas Children's Hospital, Houston, TX, USA.
  • Carlin ME; Department of Pediatrics, University of Texas, Southwestern Medical Center, Dallas, TX, USA.
  • Bader PI; Parkview Cytogenetics and Northeast Indiana Genetic Counseling Center, Fort Wayne, IN, USA.
  • Perras HM; Regional Genetics Program, Conseillère en génétique agréée, Programme régional de Génétique, Ottawa, Ontario, Canada.
  • Allanson JE; Regional Genetics Program, Conseillère en génétique agréée, Programme régional de Génétique, Ottawa, Ontario, Canada.
  • Newman L; Scott and White Memorial Hospital, Temple, TX, USA.
  • Simpson G; Especially for Children, Austin, TX, USA.
  • Immken L; Especially for Children, Austin, TX, USA.
  • Powell E; Department of Pediatrics, Vanderbilt School of Medicine, Nashville, TN, USA.
  • Mohanty A; Department of Neurosurgery, University of Texas Medical Branch, Galveston, TX, USA.
  • Kang SH; 1] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA [2] Allina Medical Laboratories, Minneapolis, MN, USA.
  • Stankiewicz P; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Bacino CA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Bi W; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Patel A; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Cheung SW; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
Eur J Hum Genet ; 23(1): 54-60, 2015 Jan.
Article en En | MEDLINE | ID: mdl-24736736
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anomalías Múltiples / Cromosomas Humanos Par 6 / Encéfalo / Deleción Cromosómica Tipo de estudio: Prognostic_studies Límite: Child, preschool / Female / Humans / Infant / Newborn Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Anomalías Múltiples / Cromosomas Humanos Par 6 / Encéfalo / Deleción Cromosómica Tipo de estudio: Prognostic_studies Límite: Child, preschool / Female / Humans / Infant / Newborn Idioma: En Revista: Eur J Hum Genet Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Estados Unidos