Publications by authors named "Devin M Cox"

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Hereditary cancer screening: Case reports and review of literature on ten Ashkenazi Jewish founder mutations.
Devin M Cox, Katherine L Nelson, Meera Clytone, Debra L Collins

Mol Genet Genomic Med· November 2018

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Response to "A Psychological Perspective on Factors Predicting Prophylactic Salpingo-Oophorectomy in a Sample of Italian Women from the General Population. Results from a Hypothetical Study in the Context of BRCA Mutations".
Devin M Cox

J Genet Couns· September 2018

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Growth Charts for Prader-Willi Syndrome During Growth Hormone Treatment.
Merlin G Butler, Jaehoon Lee, Devin M Cox, Ann M Manzardo, June-Anne Gold

Clin Pediatr (Phila)· September 2016

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The 7q11.23 Microduplication Syndrome: A Clinical Report with Review of Literature.
Elham Abbas, Devin M Cox, Teri Smith, Merlin G Butler

J Pediatr Genet· September 2016

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Distal Partial Trisomy 15q26 and Partial Monosomy 16p13.3 in a 36-Year-Old Male with Clinical Features of Both Chromosomal Abnormalities.
Devin M Cox, Merlin G Butler

Cytogenet Genome Res· September 2015

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A clinical case report and literature review of the 3q29 microdeletion syndrome.
Devin M Cox, Merlin G Butler

Clin Dysmorphol· July 2015

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Partial Deletion of Chromosome 1p31.1 Including only the Neuronal Growth Regulator 1 Gene in Two Siblings.
Ann Genovese, Devin M Cox, Merlin G Butler

J Pediatr Genet· March 2015

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A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome.
Devin M Cox, Merlin G Butler

J Pediatr Genet· March 2015

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The 15q11.2 BP1-BP2 microdeletion syndrome: a review.
Devin M Cox, Merlin G Butler

Int J Mol Sci· February 2015

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