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Prenatal exome sequencing: A useful tool for the fetal neurologist.
de Koning, Maayke A; Hoffer, Mariëtte J V; Nibbeling, Esther A R; Bijlsma, Emilia K; Toirkens, Menno J P; Adama-Scheltema, Phebe N; Verweij, E Joanne; Veenhof, Marieke B; Santen, Gijs W E; Peeters-Scholte, Cacha M P C D.
Afiliación
  • de Koning MA; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Hoffer MJV; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Nibbeling EAR; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Bijlsma EK; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Toirkens MJP; Department of Radiology, Leiden University Medical Centre, Leiden, The Netherlands.
  • Adama-Scheltema PN; Department of Obstetrics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Verweij EJ; Department of Obstetrics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Veenhof MB; Department of Obstetrics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Santen GWE; Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.
  • Peeters-Scholte CMPCD; Department of Neurology, Leiden University Medical Centre, Leiden, The Netherlands.
Clin Genet ; 101(1): 65-77, 2022 01.
Article en En | MEDLINE | ID: mdl-34611884

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Feto / Secuenciación del Exoma / Malformaciones del Sistema Nervioso Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Diagnóstico Prenatal / Feto / Secuenciación del Exoma / Malformaciones del Sistema Nervioso Tipo de estudio: Diagnostic_studies / Prognostic_studies Idioma: En Revista: Clin Genet Año: 2022 Tipo del documento: Article