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Inactivation of AMMECR1 is associated with growth, bone, and heart alterations.
Moysés-Oliveira, Mariana; Giannuzzi, Giuliana; Fish, Richard J; Rosenfeld, Jill A; Petit, Florence; Soares, Maria de Fatima; Kulikowski, Leslie Domenici; Di-Battista, Adriana; Zamariolli, Malú; Xia, Fan; Liehr, Thomas; Kosyakova, Nadezda; Carvalheira, Gianna; Parker, Michael; Seaby, Eleanor G; Ennis, Sarah; Gilbert, Rodney D; Hagelstrom, R Tanner; Cremona, Maria L; Li, Wenhui L; Malhotra, Alka; Chandrasekhar, Anjana; Perry, Denise L; Taft, Ryan J; McCarrier, Julie; Basel, Donald G; Andrieux, Joris; Stumpp, Taiza; Antunes, Fernanda; Pereira, Gustavo José; Neerman-Arbez, Marguerite; Meloni, Vera Ayres; Drummond-Borg, Margaret; Melaragno, Maria Isabel; Reymond, Alexandre.
Affiliation
  • Moysés-Oliveira M; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Giannuzzi G; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Fish RJ; Center for Integrative Genomics, University of Lausanne, Lausanne, Switzerland.
  • Rosenfeld JA; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.
  • Petit F; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Soares MF; Clinique de Génétique, CHU Lille - Hôpital Jeanne de Flandre, Lille, France.
  • Kulikowski LD; Psychobiology Department, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Di-Battista A; Department of Pathology, Laboratório de Citogenômica, LIM 03, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, São Paulo, Brazil.
  • Zamariolli M; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Xia F; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Liehr T; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Kosyakova N; Universitätsklinikum Jena, Institut für Humangenetik, Jena, Germany.
  • Carvalheira G; Universitätsklinikum Jena, Institut für Humangenetik, Jena, Germany.
  • Parker M; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Seaby EG; Sheffield Clinical Genetics Service, Sheffield Children's Hospital, Sheffield, United Kingdom.
  • Ennis S; Genomic Informatics Group, University Hospital Southampton, Southampton, United Kingdom.
  • Gilbert RD; Genomic Informatics Group, University Hospital Southampton, Southampton, United Kingdom.
  • Hagelstrom RT; Southampton Children's Hospital, University Hospital Southampton, Southampton, United Kingdom.
  • Cremona ML; Illumina Clinical Services Laboratory, San Diego, California.
  • Li WL; Illumina Clinical Services Laboratory, San Diego, California.
  • Malhotra A; Illumina Clinical Services Laboratory, San Diego, California.
  • Chandrasekhar A; Illumina Clinical Services Laboratory, San Diego, California.
  • Perry DL; Illumina Clinical Services Laboratory, San Diego, California.
  • Taft RJ; Illumina Clinical Services Laboratory, San Diego, California.
  • McCarrier J; Illumina Clinical Services Laboratory, San Diego, California.
  • Basel DG; Department of Pediatrics, Section of Genetics, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Andrieux J; Department of Pediatrics, Section of Genetics, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Stumpp T; Institut de Génétique Médicale, CHU Lille - Hôpital Jeanne de Flandre, Lille, France.
  • Antunes F; Developmental Biology Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Pereira GJ; Department of Pharmacology, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Neerman-Arbez M; Department of Pharmacology, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Meloni VA; Department of Genetic Medicine and Development, University of Geneva Medical School, Geneva, Switzerland.
  • Drummond-Borg M; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
  • Melaragno MI; Cook Children's Genetic Clinic, Fort Worth, Texas.
  • Reymond A; Genetics Division, Department of Morphology and Genetics, Universidade Federal de São Paulo, São Paulo, Brazil.
Hum Mutat ; 39(2): 281-291, 2018 02.
Article in En | MEDLINE | ID: mdl-29193635
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone and Bones / Proteins / Heart Type of study: Risk_factors_studies Limits: Animals / Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: Brazil
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bone and Bones / Proteins / Heart Type of study: Risk_factors_studies Limits: Animals / Female / Humans / Male Language: En Journal: Hum Mutat Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: Brazil