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Table representation of search results timeline featuring number of search results per year.

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1989 1
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Related Articles by Review for PMID: 32491315

37 results

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Page 1
Genetics, X-Linked Inheritance.
Basta M, Pandya AM. Basta M, et al. 2023 May 1. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. 2023 May 1. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2025 Jan–. PMID: 32491315 Free Books & Documents.
Incontinentia Pigmenti.
Scheuerle AE, Ursini MV. Scheuerle AE, et al. 1999 Jun 8 [updated 2017 Dec 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 1999 Jun 8 [updated 2017 Dec 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 20301645 Free Books & Documents. Review.
[Genetics of dilated cardiomyopathy].
Osterziel KJ, Scheffold T, Perrot A, Dietz R; Netzwerk Myokardiale Erkrankungen. Osterziel KJ, et al. Z Kardiol. 2001 Jul;90(7):461-9. doi: 10.1007/s003920170134. Z Kardiol. 2001. PMID: 11515275 Review. German.
The heart in Fabry's disease.
Sheppard MN. Sheppard MN. Cardiovasc Pathol. 2011 Jan-Feb;20(1):8-14. doi: 10.1016/j.carpath.2009.10.003. Epub 2009 Nov 17. Cardiovasc Pathol. 2011. PMID: 19919901 Review.
X-Linked Acrogigantism.
Iacovazzo D, Korbonits M. Iacovazzo D, et al. 2018 Feb 1. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. 2018 Feb 1. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025. PMID: 29389097 Free Books & Documents. Review.
General aspects of X-linked diseases.
Germain DP. Germain DP. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry Disease: Perspectives from 5 Years of FOS. Oxford: Oxford PharmaGenesis; 2006. Chapter 7. In: Mehta A, Beck M, Sunder-Plassmann G, editors. Fabry Disease: Perspectives from 5 Years of FOS. Oxford: Oxford PharmaGenesis; 2006. Chapter 7. PMID: 21290690 Free Books & Documents. Review.
Rett syndrome: the complex nature of a monogenic disease.
Renieri A, Meloni I, Longo I, Ariani F, Mari F, Pescucci C, Cambi F. Renieri A, et al. J Mol Med (Berl). 2003 Jun;81(6):346-54. doi: 10.1007/s00109-003-0444-9. Epub 2003 May 16. J Mol Med (Berl). 2003. PMID: 12750821 Review.
37 results