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Page 1
Warburg Micro syndrome.
Dursun F, Güven A, Morris-Rosendahl D. Dursun F, et al. J Pediatr Endocrinol Metab. 2012;25(3-4):379-82. doi: 10.1515/jpem-2011-0459. J Pediatr Endocrinol Metab. 2012. PMID: 22768674
A glossary of relevant genetic terms.
Morris-Rosendahl DJ. Morris-Rosendahl DJ. Dialogues Clin Neurosci. 2010;12(1):116-20. doi: 10.31887/DCNS.2010.12.1/dmrosendahl. Dialogues Clin Neurosci. 2010. PMID: 20373673 Free PMC article. No abstract available.
Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability.
Bisschoff IJ, Zeschnigk C, Horn D, Wellek B, Rieß A, Wessels M, Willems P, Jensen P, Busche A, Bekkebraten J, Chopra M, Hove HD, Evers C, Heimdal K, Kaiser AS, Kunstmann E, Robinson KL, Linné M, Martin P, McGrath J, Pradel W, Prescott KE, Roesler B, Rudolf G, Siebers-Renelt U, Tyshchenko N, Wieczorek D, Wolff G, Dobyns WB, Morris-Rosendahl DJ. Bisschoff IJ, et al. Hum Mutat. 2013 Jan;34(1):237-47. doi: 10.1002/humu.22224. Epub 2012 Oct 17. Hum Mutat. 2013. PMID: 23033313 Free PMC article.
The role of genetics and genomics in clinical psychiatry.
Hoehe MR, Morris-Rosendahl DJ. Hoehe MR, et al. Dialogues Clin Neurosci. 2018 Sep;20(3):169-177. doi: 10.31887/DCNS.2018.20.3/mhoehe. Dialogues Clin Neurosci. 2018. PMID: 30581286 Free PMC article. Review.
Filamin A mutation is one cause of FG syndrome.
Unger S, Mainberger A, Spitz C, Bähr A, Zeschnigk C, Zabel B, Superti-Furga A, Morris-Rosendahl DJ. Unger S, et al. Am J Med Genet A. 2007 Aug 15;143A(16):1876-9. doi: 10.1002/ajmg.a.31751. Am J Med Genet A. 2007. PMID: 17632775
86 results