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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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1974 | 1 |
1995 | 1 |
1999 | 1 |
2003 | 1 |
2024 | 0 |
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Mohr syndrome: a rare case and distinction from orofacial digital syndrome 1.
J Postgrad Med. 1999 Oct-Dec;45(4):123-4.
J Postgrad Med. 1999.
PMID: 10734352
Free article.
In view of the different modes of inheritance and the different prognoses of the two oro-facio-digital syndromes, type 1 and type 2, it is important to establish a correct diagnosis in these patients. ...
In view of the different modes of inheritance and the different prognoses of the two oro-facio-digital syndromes, type 1 and type 2, …
Multiple recurrent and de novo odontogenic keratocysts associated with oral-facial-digital syndrome.
Lindeboom JA, Kroon FH, de Vires J, van den Akker HP.
Lindeboom JA, et al.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003 Apr;95(4):458-62. doi: 10.1067/moe.2003.35.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2003.
PMID: 12686930
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Mohr syndrome with subclinical expression of the bifid great toe.
Levy EP, Fletcher BD, Fraser FC.
Levy EP, et al.
Am J Dis Child. 1974 Oct;128(4):531-3. doi: 10.1001/archpedi.1974.02110290101019.
Am J Dis Child. 1974.
PMID: 4414705
No abstract available.
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Short rib-dysplasia group (with/without polydactyly): report of a patient suggesting the existence of a continuous spectrum.
Franceschini P, Guala A, Vardeu MP, Signorile F, Franceschini D, Bolgiani MP.
Franceschini P, et al.
Am J Med Genet. 1995 Nov 20;59(3):359-64. doi: 10.1002/ajmg.1320590316.
Am J Med Genet. 1995.
PMID: 8599362
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