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

Year Number of Results
2008 2
2009 2
2010 6
2011 1
2012 4
2013 4
2014 3
2015 5
2016 4
2017 2
2018 4
2019 1
2020 1
2023 2
2024 0

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Did you mean intra grain[Author] (2 results)?
Multilocus methylation defects in imprinting disorders.
Mackay DJ, Eggermann T, Buiting K, Garin I, Netchine I, Linglart A, de Nanclares GP. Mackay DJ, et al. Among authors: garin i. Biomol Concepts. 2015 Mar;6(1):47-57. doi: 10.1515/bmc-2014-0037. Biomol Concepts. 2015. PMID: 25581766 Free article. Review.
Brachydactyly E: isolated or as a feature of a syndrome.
Pereda A, Garin I, Garcia-Barcina M, Gener B, Beristain E, Ibañez AM, Perez de Nanclares G. Pereda A, et al. Among authors: garin i. Orphanet J Rare Dis. 2013 Sep 12;8:141. doi: 10.1186/1750-1172-8-141. Orphanet J Rare Dis. 2013. PMID: 24028571 Free PMC article. Review.
From pseudohypoparathyroidism to inactivating PTH/PTHrP signalling disorder (iPPSD), a novel classification proposed by the EuroPHP network.
Thiele S, Mantovani G, Barlier A, Boldrin V, Bordogna P, De Sanctis L, Elli FM, Freson K, Garin I, Grybek V, Hanna P, Izzi B, Hiort O, Lecumberri B, Pereda A, Saraff V, Silve C, Turan S, Usardi A, Werner R, de Nanclares GP, Linglart A. Thiele S, et al. Among authors: garin i. Eur J Endocrinol. 2016 Dec;175(6):P1-P17. doi: 10.1530/EJE-16-0107. Epub 2016 Jul 11. Eur J Endocrinol. 2016. PMID: 27401862 Free article. Review.
Progressive osseous heteroplasia caused by a mosaic GNAS mutation.
Pereda A, Martos-Tello JM, Garin I, Errea-Dorronsoro J, Perez de Nanclares G. Pereda A, et al. Among authors: garin i. Clin Endocrinol (Oxf). 2018 Jun;88(6):993-995. doi: 10.1111/cen.13584. Epub 2018 Mar 25. Clin Endocrinol (Oxf). 2018. PMID: 29464731 No abstract available.
Clinical utility gene card for: pseudohypoparathyroidism.
Mantovani G, Linglart A, Garin I, Silve C, Elli FM, de Nanclares GP. Mantovani G, et al. Among authors: garin i. Eur J Hum Genet. 2013 Jun;21(6). doi: 10.1038/ejhg.2012.211. Epub 2012 Sep 12. Eur J Hum Genet. 2013. PMID: 22968134 Free PMC article. No abstract available.
36 results