Autosomal dominant inheritance with sex-limited manifestation: The jury is still out.

American Journal of Medical Genetics Part AVolume 191, Issue 6 p. 1675-1676 CORRESPONDENCE Autosomal dominant inheritance with sex-limited manifestation: The jury is still out Patrick J. Morrison, Patrick J. Morrison orcid.org/0000-0002-2823-1762 Patrick G Johnston Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast, UKSearch for more papers by this author Patrick J. Morrison, Patrick J. Morrison orcid.org/0000-0002-2823-1762 Patrick G Johnston Centre for Cancer Research and Cell Biology, Queens University Belfast, Belfast, UKSearch for more papers by this author First published: 24 April 2023 https://doi.org/10.1002/ajmg.a.63161Citations: 1Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL No abstract is available for this article. REFERENCES Erickson, R. P., Lai, L. W., Mustacich, D. J., Bernas, M. J., Kuo, P. H., & Witte, M. H. (2019). Sex-limited penetrance of lymphedema to females with CELSR1 haploinsufficiency: A second family. Clinical Genetics, 96(5), 478– 482. https://doi.org/10.1111/cge.13622. PMID: 31403174. Gonzalez-Garay, M. L., Aldrich, M. B., Rasmussen, J. C., Guilliod, R., Lapinski, P. E., King, P. D., & Sevick-Muraca, E. M. (2016). A novel mutation in CELSR1 is associated with hereditary lymphedema. Vascular Cell, 8, 1. https://doi.org/10.1186/s13221-016-0035-5. PMID: 26855770. Happle, R., & Eyerich, K. (2022). Autosomal dominant inheritance with sex-limited manifestation: An unusual mode of transmission in humans and animals. American Journal of Medical Genetics. Part A, 191, 684– 689. https://doi.org/10.1002/ajmg.a.63073. PMID: 36538935. Morrison, P. J., Znaczko, A., & Jansson, M. (2020). Paternal somatogonadal COL2A1 mosaicism causing recurrence of severe type 2 collagenopathy. American Journal of Medical Genetics. Part A, 182(9), 2191– 2194. https://doi.org/10.1002/ajmg.a.6176 Citing Literature Volume191, Issue6June 2023Pages 1675-1676 ReferencesRelatedInformation