نتائج البحث - Megan Rech
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1
Schaaf‐Yang syndrome overview: Report of 78 individuals حسب John McCarthy, Philip J. Lupo, Erin Kovar, Megan Rech, Bret L. Bostwick, Daryl A. Scott, Katerina Kraft, Tony Roscioli, Joel Charrow, Samantha A. Schrier Vergano, Edward J. Lose, Robert Smiegel, Yves Lacassie, Christian P. Schaaf
منشور في 2018Artigo -
2
Phenotypic expansion of <scp>Bosch–Boonstra–Schaaf</scp> optic atrophy syndrome and further evidence for genotype–phenotype correlations حسب Megan Rech, John McCarthy, Chun‐An Chen, Jane C. Edmond, Veeral S. Shah, Daniëlle G.M. Bosch, Gerard T. Berry, Linford Williams, Suneeta Madan‐Khetarpal, Dmitriy Niyazov, Charles Shaw‐Smith, Erin Kovar, Philip J. Lupo, Christian P. Schaaf
منشور في 2020Artigo -
3
Pathogenic variants in USP7 cause a neurodevelopmental disorder with speech delays, altered behavior, and neurologic anomalies حسب Michael D. Fountain, David S. Oleson, Megan Rech, Lara Segebrecht, Jill V. Hunter, John McCarthy, Philip J. Lupo, Manuel Holtgrewe, Rocio Moran, Jill A. Rosenfeld, Bertrand Isidor, Cédric Le Caignec, Margarita Sáenz, Robert C. Pedersen, Thomas M. Morgan, Jean P. Pfotenhauer, Fan Xia, Weimin Bi, Sung-Hae L. Kang, Ankita Patel, Ian D. Krantz, Sarah E. Raible, Wendy E. Smith, Ingrid Cristian, Erin Torti, Jane Juusola, Francisca Millan, Ingrid M. Wentzensen, Richard Person, Sébastien Küry, Stéphane Bézieau, Kévin Uguen, Claude Férec, Arnold Münnich, Mieke M. van Haelst, Klaske D. Lichtenbelt, Koen L.I. van Gassen, Tanner Hagelstrom, Aditi Chawla, Denise Perry, Ryan J. Taft, Marilyn C. Jones, Diane Masser‐Frye, David A. Dyment, Sunita Venkateswaran, Chumei Li, Luis Escobar, Denise Horn, Rebecca C. Spillmann, Loren D.M. Peña, Jolanta Wierzba, Tim M. Strom, Ilaria Parenti, Frank J. Kaiser, Nadja Ehmke, Christian P. Schaaf
منشور في 2019Artigo
أدوات البحث:
موضوعات ذات صلة
Autism
Autism spectrum disorder
Biology
Gene
Genetics
Hypotonia
Intellectual disability
Medicine
Neurodevelopmental disorder
Phenotype
Frameshift mutation
Internal medicine
Psychiatry
Psychology
Atrophy
Bioinformatics
Cohort
Developmental psychology
Disease
Epilepsy
Exome sequencing
Global developmental delay
Haploinsufficiency
Hypoplasia
Neuroscience
Optic nerve
Optic nerve hypoplasia
Pathology
Pediatrics
Speech delay