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Results by year

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

Year Number of Results
1952 1
1958 1
1959 1
1962 1
1965 1
1966 1
1967 2
1972 1
1973 1
1974 1
1976 2
1977 7
1978 5
1979 7
1980 6
1981 1
1982 3
1983 4
1984 3
1985 3
1986 5
1987 6
1988 6
1989 4
1990 10
1991 7
1992 8
1993 3
1994 2
1995 4
1996 7
1997 8
1998 12
1999 11
2000 5
2001 11
2002 3
2003 13
2004 6
2005 6
2006 4
2007 4
2008 3
2009 1
2011 2
2013 1
2014 1
2016 1
2017 1
2024 0

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PubMed (OMIM) for id: 650

206 results

Results by year

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Page 1
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 Deletions.
Tan TY, Gonzaga-Jauregui C, Bhoj EJ, Strauss KA, Brigatti K, Puffenberger E, Li D, Xie L, Das N, Skubas I, Deckelbaum RA, Hughes V, Brydges S, Hatsell S, Siao CJ, Dominguez MG, Economides A, Overton JD, Mayne V, Simm PJ, Jones BO, Eggers S, Le Guyader G, Pelluard F, Haack TB, Sturm M, Riess A, Waldmueller S, Hofbeck M, Steindl K, Joset P, Rauch A, Hakonarson H, Baker NL, Farlie PG. Tan TY, et al. Am J Hum Genet. 2017 Dec 7;101(6):985-994. doi: 10.1016/j.ajhg.2017.10.006. Epub 2017 Nov 30. Am J Hum Genet. 2017. PMID: 29198724 Free PMC article.
Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles.
Timberlake AT, Choi J, Zaidi S, Lu Q, Nelson-Williams C, Brooks ED, Bilguvar K, Tikhonova I, Mane S, Yang JF, Sawh-Martinez R, Persing S, Zellner EG, Loring E, Chuang C, Galm A, Hashim PW, Steinbacher DM, DiLuna ML, Duncan CC, Pelphrey KA, Zhao H, Persing JA, Lifton RP. Timberlake AT, et al. Elife. 2016 Sep 8;5:e20125. doi: 10.7554/eLife.20125. Elife. 2016. PMID: 27606499 Free PMC article.
Increased height in HFE hemochromatosis.
Cippà PE, Krayenbuehl PA. Cippà PE, et al. N Engl J Med. 2013 Aug 22;369(8):785-6. doi: 10.1056/NEJMc1303066. N Engl J Med. 2013. PMID: 23964954 Free article. No abstract available.
206 results