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7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder.
Rieger, Melissa; Krumbiegel, Mandy; Reuter, Miriam S; Schützenberger, Anne; Reis, André; Zweier, Christiane.
Affiliation
  • Rieger M; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Krumbiegel M; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Reuter MS; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Schützenberger A; Division of Phoniatrics and Pediatric Audiology, Department of Otorhinolaryngology, Head and Neck Surgery, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Reis A; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
  • Zweier C; Institute of Human Genetics, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany.
Am J Med Genet A ; 182(11): 2737-2741, 2020 11.
Article in En | MEDLINE | ID: mdl-32885567
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Speech Disorders / Chromosomes, Human, Pair 7 / Chromosome Deletion / Forkhead Transcription Factors / Language Disorders Type of study: Prognostic_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phenotype / Speech Disorders / Chromosomes, Human, Pair 7 / Chromosome Deletion / Forkhead Transcription Factors / Language Disorders Type of study: Prognostic_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2020 Document type: Article Affiliation country: Alemania Country of publication: Estados Unidos