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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2000 | 1 |
2001 | 1 |
2002 | 2 |
2006 | 1 |
2024 | 0 |
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Page 1
A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva.
Nat Genet. 2006 May;38(5):525-7. doi: 10.1038/ng1783. Epub 2006 Apr 23.
Nat Genet. 2006.
PMID: 16642017
Reported noggin mutations are PCR errors.
Xu MQ, Shore EM, Kaplan FS.
Xu MQ, et al.
Am J Med Genet. 2002 Apr 22;109(2):161; author reply 163-4. doi: 10.1002/ajmg.10288.
Am J Med Genet. 2002.
PMID: 11977168
No abstract available.
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Significant difference of opinion regarding the role of noggin in fibrodysplasia ossificans progressiva.
Warman ML.
Warman ML.
Am J Med Genet. 2002 Apr 22;109(2):162; author reply 163-4. doi: 10.1002/ajmg.10290.
Am J Med Genet. 2002.
PMID: 11977169
No abstract available.
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Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP).
Xu MQ, Feldman G, Le Merrer M, Shugart YY, Glaser DL, Urtizberea JA, Fardeau M, Connor JM, Triffitt J, Smith R, Shore EM, Kaplan FS.
Xu MQ, et al.
Clin Genet. 2000 Oct;58(4):291-8. doi: 10.1034/j.1399-0004.2000.580407.x.
Clin Genet. 2000.
PMID: 11076054
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Identification of three novel mutations of the noggin gene in patients with fibrodysplasia ossificans progressiva.
Sémonin O, Fontaine K, Daviaud C, Ayuso C, Lucotte G.
Sémonin O, et al.
Am J Med Genet. 2001 Sep 1;102(4):314-7. doi: 10.1002/ajmg.1504.
Am J Med Genet. 2001.
PMID: 11503156
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