Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.

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Bibliographic Details
Title: Elucidation of the phenotypic spectrum and genetic landscape in primary and secondary microcephaly.
Authors: Boonsawat P; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Joset P; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Steindl K; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Oneda B; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Gogoll L; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Azzarello-Burri S; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Sheth F; FRIGE's Institute of Human Genetics, FRIGE House, Satellite, Ahmedabad, India., Datar C; Sahyadri Medical Genetics and Tissue Engineering Facility, Kothrud, Pune and Bharati Hospital and Research Center Dhankawadi, Pune, India., Verma IC; Institute of Medical Genetics & Genomics, Sir Ganga Ram Hospital, Rajinder Nagar, New Delhi, India., Puri RD; Institute of Medical Genetics & Genomics, Sir Ganga Ram Hospital, Rajinder Nagar, New Delhi, India., Zollino M; Unità Operativa Complessa di Genetica Medica, Fondazione Policlinico Universitario A. Gemelli IRCCS, and Istituto di Medicina Genomica, Università Cattolica del Sacro Cuore, Rome, Italy., Bachmann-Gagescu R; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Niedrist D; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Papik M; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Figueiro-Silva J; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Masood R; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Zweier M; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Kraemer D; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Lincoln S; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA., Rodan L; Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.; Department of Neurology, Boston Children's Hospital, Boston, MA, USA., Passemard S; Service de Neuropédiatrie, Hôpital Universitaire Robert Debré, APHP, Paris, France.; Département de Génétique, Hôpital Universitaire Robert Debré, APHP, Paris, France., Drunat S; Département de Génétique, Hôpital Universitaire Robert Debré, APHP, Paris, France., Verloes A; Département de Génétique, Hôpital Universitaire Robert Debré, APHP, Paris, France., Horn AHC; Division of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Sticht H; Division of Bioinformatics, Institute of Biochemistry, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany., Steinfeld R; Division of Pediatric Neurology, University Children's Hospital Zurich, Zurich, Switzerland., Plecko B; Division of Pediatric Neurology, University Children's Hospital Zurich, Zurich, Switzerland.; Department of Pediatrics and Adolescent Medicine, Division of General Pediatrics, Medical University of Graz, Graz, Austria., Latal B; Child Development Center, University Children's Hospital Zurich, Zurich, Switzerland., Jenni O; Child Development Center, University Children's Hospital Zurich, Zurich, Switzerland., Asadollahi R; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland., Rauch A; Institute of Medical Genetics, University of Zurich, Schlieren, Zurich, Switzerland. anita.rauch@medgen.uzh.ch.; Neuroscience Center Zurich, University of Zurich, Zurich, Switzerland. anita.rauch@medgen.uzh.ch.; Zurich Center of Integrative Human Physiology, University of Zurich, Zurich, Switzerland. anita.rauch@medgen.uzh.ch.
Corporate Authors: Undiagnosed Diseases Network (UDN)
Source: Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2019 Sep; Vol. 21 (9), pp. 2043-2058. Date of Electronic Publication: 2019 Mar 07.
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Elsevier Country of Publication: United States NLM ID: 9815831 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1530-0366 (Electronic) Linking ISSN: 10983600 NLM ISO Abbreviation: Genet Med Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1530-0366
DOI:10.1038/s41436-019-0464-7