Hall RK - Search Results

1

SHH mutation is associated with solitary median maxillary central incisor: a study of 13 patients and review of the literature.

Nanni L, Ming JE, Du Y, Hall RK, Aldred M, Bankier A, Muenke M. Nanni L, et al. Among authors: hall rk. Am J Med Genet. 2001 Jul 22;102(1):1-10. doi: 10.1002/1096-8628(20010722)102:1<1::aid-ajmg1336>3.0.co;2-u. Am J Med Genet. 2001. PMID: 11471164 Review.

2

Solitary median maxillary central incisor, short stature, choanal atresia/midnasal stenosis (SMMCI) syndrome.

Hall RK, Bankier A, Aldred MJ, Kan K, Lucas JO, Perks AG. Hall RK, et al. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1997 Dec;84(6):651-62. doi: 10.1016/s1079-2104(97)90368-1. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1997. PMID: 9431535 Review.

3

Molecular analysis for genetic counselling in amelogenesis imperfecta.

Aldred MJ, Hall RK, Kilpatrick N, Bankier A, Savarirayan R, Lamandé SR, Lench NJ, Crawford PJ. Aldred MJ, et al. Among authors: hall rk. Oral Dis. 2002 Sep;8(5):249-53. doi: 10.1034/j.1601-0825.2002.02835.x. Oral Dis. 2002. PMID: 12363109

4

Gingival fibromatosis and Klippel-Trénaunay-Weber syndrome. Case report.

Hallett KB, Bankier A, Chow CW, Bateman J, Hall RK. Hallett KB, et al. Among authors: hall rk. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995 May;79(5):578-82. doi: 10.1016/s1079-2104(05)80099-x. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995. PMID: 7600221

5

Solitary median maxillary central incisor (SMMCI) syndrome.

Hall RK. Hall RK. Orphanet J Rare Dis. 2006 Apr 9;1:12. doi: 10.1186/1750-1172-1-12. Orphanet J Rare Dis. 2006. PMID: 16722608 Free PMC article. Review.

6

A syndrome of epilepsy, dementia, and amelogenesis imperfecta: genetic and clinical features.

Christodoulou J, Hall RK, Menahem S, Hopkins IJ, Rogers JG. Christodoulou J, et al. Among authors: hall rk. J Med Genet. 1988 Dec;25(12):827-30. doi: 10.1136/jmg.25.12.827. J Med Genet. 1988. PMID: 3236364 Free PMC article.

7

Solitary median maxillary central incisor syndrome occurring together with oromandibular-limb hypogenesis syndrome type 1: a case report of this previously unreported combination of syndromes.

Lertsirivorakul J, Hall RK. Lertsirivorakul J, et al. Among authors: hall rk. Int J Paediatr Dent. 2008 Jul;18(4):306-11. doi: 10.1111/j.1365-263X.2007.00907.x. Epub 2008 Mar 6. Int J Paediatr Dent. 2008. PMID: 18328045

8

The clinical features of spondyloepiphyseal dysplasia congenita resulting from the substitution of glycine 997 by serine in the alpha 1(II) chain of type II collagen.

Cole WG, Hall RK, Rogers JG. Cole WG, et al. Among authors: hall rk. J Med Genet. 1993 Jan;30(1):27-35. doi: 10.1136/jmg.30.1.27. J Med Genet. 1993. PMID: 8423604 Free PMC article.

9

Aggressive infantile fibromatosis: report of a case undergoing spontaneous regression.

Hoffman CD, Levant BA, Hall RK. Hoffman CD, et al. Among authors: hall rk. J Oral Maxillofac Surg. 1993 Sep;51(9):1043-7. doi: 10.1016/s0278-2391(10)80054-0. J Oral Maxillofac Surg. 1993. PMID: 8355096 No abstract available.

10

Mucopolysaccharidosis: MPS VI and associated delayed tooth eruption.

Smith KS, Hallett KB, Hall RK, Wardrop RW, Firth N. Smith KS, et al. Among authors: hall rk. Int J Oral Maxillofac Surg. 1995 Apr;24(2):176-80. doi: 10.1016/s0901-5027(06)80097-4. Int J Oral Maxillofac Surg. 1995. PMID: 7608587

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

113 results

Search Page

Filters