Publications by authors named "Robert F Stratton"

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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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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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