Dhir A, Li R, Li G, Dean J, Robin NH, Alva E. (2020) Simultaneous osteosarcoma and renal cell carcinoma with BRCA1 mutation in a young male adult with prior oligodendroglioma.Pediatr Blood Cancer. 2020 Mar;67(3):e28116. |
31850619 |
Perry TJ, Patton SI, Farmer MB, Hurst CB, McGwin G, Robin NH.(2020). The duty to warn at-risk relatives-The experience of genetic counselors and medical geneticists. Am J Med Genet A. 2020 Feb;182(2):314-321 |
31850619 |
Gooch C, Robin NH, Hurst ACE. (2019) Neonatal management of achondroplasia: one hospital's geosocial approach to improve patient outcomes.Curr Opin Pediatr. 2019 Dec;31(6):691-693 |
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Upadia J, Gonzales PR, Atkinson TP, Schroeder HW, Robin NH, Rudy NL, Mikhail FM.(2018) A previously unrecognized 22q13.2 microdeletion syndrome that encompasses TCF20 and TNFRSF13C. Am J Med Genet A. 2018 Dec;176(12):2791-2797. |
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Hamm JA, Nichols M, Robin NH (2017). Program Directors’ Opinions on Medical Genetics Education in Pediatric Residency Programs. Curr Opin Peds. 29(6):619-62. |
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Jacobs AP, Subramaniam A, Tang Y, Philips JB 3rd, Biggio JR, Edwards RK, Robin NH (2016). Trisomy 18: A survey of opinions, attitudes, and practices of neonatologists.Am J Med Genet A. 2016 Oct;170(10):2638-43. |
27312333 |
American College of Medical Genetics and Genomics working group (2014). Guidelines on the genetic evaluation of hearing loss Genet Med. 16:347-55. |
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Robin NH.(2018)Teaching dysmorphology in the era of genomics: new technologies, new learners. Curr Opin Pediatr. 2018 Dec;30(6):699-700. |
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Robin NH, Farmer MB. Pediatric Cancer Genetics. Elsevier (2017) (https://www.us.elsevierhealth.com/pediatric-cancer-genetics-9780323485555.html) |
ISBN 9780323485555 |
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