Publications by authors named "Rachel A Hart"

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Severe Vitamin B12 Deficiency Mimicking Microangiopathic Hemolytic Anemia.
Ramzi Hassouneh, Steve Shen, Olivia Lee, Rachel A Hart, Logan P Rhea

J Hematol· August 2021

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Craniosynostosis and Noonan syndrome with KRAS mutations: Expanding the phenotype with a case report and review of the literature.
Yonit A Addissie, Udhaya Kotecha, Rachel A Hart, Ariel F Martinez, Paul Kruszka

Am J Med Genet A· November 2015

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Executive Function and Adaptive Behavior in Muenke Syndrome.
Colin M P Yarnell, Yonit A Addissie, Donald W Hadley, Maria J Guillen Sacoto, Nneamaka B Agochukwu, Rachel A Hart, Hartmut Collmann

J Pediatr· August 2015

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Mutations in SPECC1L, encoding sperm antigen with calponin homology and coiled-coil domains 1-like, are found in some cases of autosomal dominant Opitz G/BBB syndrome.
Paul Kruszka, Dong Li, Margaret H Harr, Nathan R Wilson, Daniel Swarr, Rachel A Hart

J Med Genet· February 2015

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Expanding the phenotypic expression of Sonic Hedgehog mutations beyond holoprosencephaly.
Paul Kruszka, Rachel A Hart, Donald W Hadley, Maximilian Muenke, Mutaz B Habal

J Craniofac Surg· January 2015

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