Publications by authors named "Robert Stratton"

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Pathogenic SPTBN1 variants cause an autosomal dominant neurodevelopmental syndrome.
Margot A Cousin, Blake A Creighton, Keith A Breau, Rebecca C Spillmann, Erin Torti, Robert Stratton

Nat Genet· July 2021

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Madelyn A Gillentine, Tianyun Wang, Kendra Hoekzema, Jill Rosenfeld, Pengfei Liu, Robert Stratton

Genome Med· April 2021

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Phenotypic spectrum and transcriptomic profile associated with germline variants in TRAF7.
Laura Castilla-Vallmanya, Kaja K Selmer, Clémantine Dimartino, Raquel Rabionet, Bernardo Blanco-Sánchez, Robert Stratton

Genet Med· July 2020

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Case of 7p22.1 Microduplication Detected by Whole Genome Microarray (REVEAL) in Workup of Child Diagnosed with Autism.
Veronica Goitia, Marcial Oquendo, Robert Stratton

Case Rep Genet· April 2015

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Establishing a reference group for distal 18q-: clinical description and molecular basis.
Jannine D Cody, Minire Hasi, Bridgette Soileau, Patricia Heard, Erika Carter, Robert F Stratton

Hum Genet· February 2014

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Metastatic medulloblastoma in an adolescent with Simpson-Golabi-Behmel syndrome.
Martha Thomas, Victoria Enciso, Robert Stratton, Shafqat Shah, Thomas Winder

Am J Med Genet A· October 2012

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Narrowing critical regions and determining penetrance for selected 18q- phenotypes.
Jannine D Cody, Patricia L Heard, Analisa C Crandall, Erika M Carter, John Li, Robert F Stratton

Am J Med Genet A· July 2009

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Recurrent interstitial deletions of proximal 18q: a new syndrome involving expressive speech delay.
Jannine D Cody, Courtney Sebold, Amtul Malik, Patricia Heard, Erika Carter, Robert F Stratton

Am J Med Genet A· June 2007

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Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation.
Frank J Probst, Elizabeth R Roeder, Victoria B Enciso, Zhishuo Ou, M Lance Cooper, Robert F Stratton

Am J Med Genet A· June 2007

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Mutations in PATCHED-1, the receptor for SONIC HEDGEHOG, are associated with holoprosencephaly.
Jeffrey E Ming, Michelle E Kaupas, Erich Roessler, Han G Brunner, Mahin Golabi, Robert F Stratton

Hum Genet· April 2002

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State interference with personhood: the privacy right, necessity defense, and proscribed medical therapies.
Robert T Stratton

Pac Law J· July 1979

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