-
1
-
-
0002381032
-
Periodontal diagnosis and diagnostic aids
-
Chicago: The American Academy of Periodontology I-1
-
Caton J. Periodontal diagnosis and diagnostic aids. In: Proceedings of the World Workshop in Clinical Periodontics. Chicago: The American Academy of Periodontology I-1, 1989.
-
(1989)
Proceedings of the World Workshop in Clinical Periodontics
-
-
Caton, J.1
-
2
-
-
0020760685
-
Prepubertal periodontitis. I. Definition of a clinical disease entity
-
Page RC, Bowen T, Altman L, et al. Prepubertal periodontitis. I. Definition of a clinical disease entity. J Periodontol 1983;54:257-71.
-
(1983)
J Periodontol
, vol.54
, pp. 257-271
-
-
Page, R.C.1
Bowen, T.2
Altman, L.3
-
3
-
-
0025246662
-
Prepubertal periodontitis: A review of diagnostic criteria, pathogenesis, and differential diagnosis
-
Watanabe K. Prepubertal periodontitis: a review of diagnostic criteria, pathogenesis, and differential diagnosis. J Periodontal Res 1990;25:31-48.
-
(1990)
J Periodontal Res
, vol.25
, pp. 31-48
-
-
Watanabe, K.1
-
4
-
-
0026860885
-
Clinical, laboratory, and immunological studies of a family with a high prevalence of generalized prepubertal and juvenile periodontitis
-
Lopez NJ. Clinical, laboratory, and immunological studies of a family with a high prevalence of generalized prepubertal and juvenile periodontitis. J Periodontol 1992;63:457-68.
-
(1992)
J Periodontol
, vol.63
, pp. 457-468
-
-
Lopez, N.J.1
-
5
-
-
0031155595
-
Possible autosomal-dominant inheritance of prepubertal periodontitis in an extended kindred
-
Shapira L, Schlesinger M, Bimstein E. Possible autosomal-dominant inheritance of prepubertal periodontitis in an extended kindred. J Clin Periodontol 1997;24:388-93.
-
(1997)
J Clin Periodontol
, vol.24
, pp. 388-393
-
-
Shapira, L.1
Schlesinger, M.2
Bimstein, E.3
-
7
-
-
0040920369
-
-
Johns Hopkins University, Baltimore, MD. MIM number: {162700}: {12/2/94}
-
Online Mendelian Inheritance in Man. OMIM™. Johns Hopkins University, Baltimore, MD. MIM number: {162700}: {12/2/94}. World Wide Web URL: http://www.ncbi.nlm.nih.gov/mim/
-
Online Mendelian Inheritance in Man. OMIM™
-
-
-
8
-
-
0040920369
-
-
Johns Hopkins University, Baltimore, MD. MIM number: {116920}: {10/8/99}
-
Online Mendelian Inheritance in Man. OMIM™. Johns Hopkins University, Baltimore, MD. MIM number: {116920}: {10/8/99}. World Wide Web URL: http://www.ncbi.nlm.nih.gov/mim/
-
Online Mendelian Inheritance in Man. OMIM™
-
-
-
9
-
-
0040920369
-
-
Johns Hopkins University, Baltimore, MD. MIM number: {266265}: {10/8/99}
-
Online Mendelian Inheritance in Man. OMIM™. Johns Hopkins University, Baltimore, MD. MIM number: {266265}: {10/8/99}. World Wide Web URL: http://www.ncbi.nlm.nih.gov/mim/
-
Online Mendelian Inheritance in Man. OMIM™
-
-
-
10
-
-
0040920369
-
-
Johns Hopkins University, Baltimore, MD. MIM number: {214500}: {11/12/99}
-
Online Mendelian Inheritance in Man. OMIM™. Johns Hopkins University, Baltimore, MD. MIM number: {214500}: {11/12/99}. World Wide Web URL: http://www.ncbi.nlm.nih.gov/mim/
-
Online Mendelian Inheritance in Man. OMIM™
-
-
-
11
-
-
0040920369
-
-
Johns Hopkins University, Baltimore, MD. MIM number: {245000}: {2/11/98}
-
Online Mendelian Inheritance in Man. OMIM™. Johns Hopkins University, Baltimore, MD. MIM number: {245000}: {2/11/98}. World Wide Web URL: http://www.ncbi.nlm.nih.gov/mim/
-
Online Mendelian Inheritance in Man. OMIM™
-
-
-
12
-
-
0030790614
-
Mapping of Papillon-Lefèvre syndrome to the chromosome 11q14 region
-
Fischer J, Blanchet-Bardon C, Prud'homme JF, et al. Mapping of Papillon-Lefèvre syndrome to the chromosome 11q14 region. Eur J Hum Genet 1997;5:156-60.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 156-160
-
-
Fischer, J.1
Blanchet-Bardon, C.2
Prud'homme, J.F.3
-
13
-
-
0031433108
-
Localization of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping
-
Laass MW, Hennies HC, Preis S, et al. Localization of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping. Hum Genet 1997;101:376-82.
-
(1997)
Hum Genet
, vol.101
, pp. 376-382
-
-
Laass, M.W.1
Hennies, H.C.2
Preis, S.3
-
14
-
-
0032169055
-
Sublocalization of the Papillon-Lefèvre syndrome locus on 11q14-q21
-
Hart TC, Bowden DW, Ghaffar KA, et al. Sublocalization of the Papillon-Lefèvre syndrome locus on 11q14-q21. Am J Med Genet 1998;79:134-9.
-
(1998)
Am J Med Genet
, vol.79
, pp. 134-139
-
-
Hart, T.C.1
Bowden, D.W.2
Ghaffar, K.A.3
-
15
-
-
1642582421
-
An integrated physical and genetic map of the PLS locus interval on chromosome 11q14
-
in press
-
Hart TC, Bowden DW, Hart PS, et al. An integrated physical and genetic map of the PLS locus interval on chromosome 11q14. Mamm Genome (in press).
-
Mamm Genome
-
-
Hart, T.C.1
Bowden, D.W.2
Hart, P.S.3
-
16
-
-
0033455594
-
Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrom
-
Hart TC, Hart PS, Bowden DW, et al. Mutations of the cathepsin C gene are responsible for Papillon-Lefèvre syndrom. J Med Genet 1999;36:881-7.
-
(1999)
J Med Genet
, vol.36
, pp. 881-887
-
-
Hart, T.C.1
Hart, P.S.2
Bowden, D.W.3
-
17
-
-
0001147550
-
The syndrome of palmo-plantar hyperkeratosis and premature periodontal destructure of the teeth
-
Gorlin RJ, Sedano H, Anderson VE. The syndrome of palmo-plantar hyperkeratosis and premature periodontal destructure of the teeth. J Pediatr 1964;65:896-908.
-
(1964)
J Pediatr
, vol.65
, pp. 896-908
-
-
Gorlin, R.J.1
Sedano, H.2
Anderson, V.E.3
-
18
-
-
0018330757
-
The Papillon-Lefèvre syndrome: Keratosis palmoplantaris with periodontopathy. Report of a case and review of the cases in the literature
-
Haneke E. The Papillon-Lefèvre syndrome: keratosis palmoplantaris with periodontopathy. Report of a case and review of the cases in the literature. Hum Genet 1979;51:1-35.
-
(1979)
Hum Genet
, vol.51
, pp. 1-35
-
-
Haneke, E.1
-
19
-
-
0029988982
-
Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas
-
Stevens HP, Kelsell DP, Bryant SP, et al. Linkage of an American pedigree with palmoplantar keratoderma and malignancy (palmoplantar ectodermal dysplasia type III) to 17q24. Literature survey and proposed updated classification of the keratodermas. Arch Dermatol 1996;132:640-51.
-
(1996)
Arch Dermatol
, vol.132
, pp. 640-651
-
-
Stevens, H.P.1
Kelsell, D.P.2
Bryant, S.P.3
-
20
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach J, Gyapay G, Dib C, et al. A second-generation linkage map of the human genome. Nature 1992;359:794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
-
21
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, et al. A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 1996,380:152-4.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
-
23
-
-
0028790963
-
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
-
O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet 1995;11:402-8.
-
(1995)
Nat Genet
, vol.11
, pp. 402-408
-
-
O'Connell, J.R.1
Weeks, D.E.2
-
24
-
-
0029918883
-
Nonparametric simulation-based statistics for detecting linkage in general pedigrees
-
Davis S, Schroeder M, Goldin LR, Weeks DE. Nonparametric simulation-based statistics for detecting linkage in general pedigrees. Am J Hum Genet 1996;58:867-80.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 867-880
-
-
Davis, S.1
Schroeder, M.2
Goldin, L.R.3
Weeks, D.E.4
-
25
-
-
0030747762
-
Exact transmission-disequilibrium tests with multiallelic markers
-
Cleves MA, Olson JM, Jacobs KB. Exact transmission-disequilibrium tests with multiallelic markers. Genet Epidemiol/1997;14:337-47.
-
(1997)
Genet Epidemiol
, vol.14
, pp. 337-347
-
-
Cleves, M.A.1
Olson, J.M.2
Jacobs, K.B.3
-
26
-
-
0003796752
-
-
Department of Epidemiology and Biostatistics, Rammelkamp Center for Education and Research, Metrohealth Campus, Case Western Reserve University, Cleveland
-
SAGE. Statistical analysis for genetic epidemiology, release 3.0. Department of Epidemiology and Biostatistics, Rammelkamp Center for Education and Research, Metrohealth Campus, Case Western Reserve University, Cleveland, 1997.
-
(1997)
SAGE. Statistical Analysis for Genetic Epidemiology, Release 3.0
-
-
-
27
-
-
0000803318
-
Construction of multilocus genetic linkage maps in humans
-
Lander ES, Green P. Construction of multilocus genetic linkage maps in humans. Proc Natl Acad Sci USA 1987;84:2363-7.
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 2363-2367
-
-
Lander, E.S.1
Green, P.2
-
28
-
-
0034056862
-
Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C
-
Hart TC, Han PS, Michalec MD, et al. Haim-Munk syndrome and Papillon-Lefèvre syndrome are allelic mutations in cathepsin C. J Med Genet 2000;37:88-94.
-
(2000)
J Med Genet
, vol.37
, pp. 88-94
-
-
Hart, T.C.1
Han, P.S.2
Michalec, M.D.3
-
29
-
-
0030278552
-
Periodontal diseases: Epidemiology
-
Papapanou PN. Periodontal diseases: epidemiology. Ann Periodontol 1996;1:1-36.
-
(1996)
Ann Periodontol
, vol.1
, pp. 1-36
-
-
Papapanou, P.N.1
-
30
-
-
0030280523
-
Periodontal diseases: Diagnosis
-
Armitage GC. Periodontal diseases: diagnosis. Ann Periodontol 1996;1:37-215.
-
(1996)
Ann Periodontol
, vol.1
, pp. 37-215
-
-
Armitage, G.C.1
-
31
-
-
0030280463
-
Periodontal diseases: Pathogenesis
-
Offenbacher S. Periodontal diseases: pathogenesis. Ann Periodontol 1996;1:821-78.
-
(1996)
Ann Periodontol
, vol.1
, pp. 821-878
-
-
Offenbacher, S.1
-
32
-
-
0031152179
-
Genetic factors in the pathogenesis of periodontitis
-
Hart TC, Kornman KS. Genetic factors in the pathogenesis of periodontitis. Periodontology 2000 1997;14:202-15.
-
(1997)
Periodontology 2000
, vol.14
, pp. 202-215
-
-
Hart, T.C.1
Kornman, K.S.2
-
33
-
-
0028451752
-
Evidence for autosomal dominant inheritance and race-specific heterogeneity in early-onset periodontitis
-
Marazita ML, Burmeister JA, Gunsolley JC, Koertge TE, Lake K, Schenkein HA. Evidence for autosomal dominant inheritance and race-specific heterogeneity in early-onset periodontitis. J Periodontol 1994;65:623-30.
-
(1994)
J Periodontol
, vol.65
, pp. 623-630
-
-
Marazita, M.L.1
Burmeister, J.A.2
Gunsolley, J.C.3
Koertge, T.E.4
Lake, K.5
Schenkein, H.A.6
-
34
-
-
0022989096
-
An autosomal-dominant form of juvenile periodontitis: Its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc
-
Boughman JA, Halloran SL, Roulston D, et al. An autosomal-dominant form of juvenile periodontitis: its localization to chromosome 4 and linkage to dentinogenesis imperfecta and Gc. J Craniofac Genet Dev Biol 1986;6:341-50.
-
(1986)
J Craniofac Genet Dev Biol
, vol.6
, pp. 341-350
-
-
Boughman, J.A.1
Halloran, S.L.2
Roulston, D.3
-
35
-
-
0027203728
-
Reevaluation of the chromosome 4q candidate region for early onset periodontitis
-
Hart TC, Marazita ML, McCanna KM, Schenkein HA, Diehl SR. Reevaluation of the chromosome 4q candidate region for early onset periodontitis. Hum Genet 1993;91:416-22.
-
(1993)
Hum Genet
, vol.91
, pp. 416-422
-
-
Hart, T.C.1
Marazita, M.L.2
McCanna, K.M.3
Schenkein, H.A.4
Diehl, S.R.5
-
36
-
-
0030293556
-
Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome
-
Nagle DL, Karim MA, Woolf EA, et al. Identification and mutation analysis of the complete gene for Chediak-Higashi syndrome. Nat Genet 1996;14:307-11.
-
(1996)
Nat Genet
, vol.14
, pp. 307-311
-
-
Nagle, D.L.1
Karim, M.A.2
Woolf, E.A.3
-
37
-
-
0022473014
-
LFA-1 immunodeficiency disease: Definition of the genetic defect and chromosomal mapping of alpha and beta subunits of the lymphocyte function-associated antigen I (LFA-1) by complementation in hybrid cells
-
Marlin SD, Morton CC, Anderson DC, Springer TA. LFA-1 immunodeficiency disease: definition of the genetic defect and chromosomal mapping of alpha and beta subunits of the lymphocyte function-associated antigen I (LFA-1) by complementation in hybrid cells. J Exp Med 1986;164:855-67.
-
(1986)
J Exp Med
, vol.164
, pp. 855-867
-
-
Marlin, S.D.1
Morton, C.C.2
Anderson, D.C.3
Springer, T.A.4
-
38
-
-
0032922549
-
A novel leukocyte adhesion deficiency caused by expressed but nonfunctional beta2 integrins Mac-1 and LFA-1
-
Hogg N, Stewart MP, Scarth SL, et al. A novel leukocyte adhesion deficiency caused by expressed but nonfunctional beta2 integrins Mac-1 and LFA-1. J Clin Invest 1999;103:97-106.
-
(1999)
J Clin Invest
, vol.103
, pp. 97-106
-
-
Hogg, N.1
Stewart, M.P.2
Scarth, S.L.3
-
39
-
-
0032537568
-
Defective intracellular activity of GDP-D-mannose-4,6-dehydratase in leukocyte adhesion deficiency type II syndrome
-
Sturla L, Etzioni A, Bisso A, et al. Defective intracellular activity of GDP-D-mannose-4,6-dehydratase in leukocyte adhesion deficiency type II syndrome. FEBS Lett 1998;429:274-8.
-
(1998)
FEBS Lett
, vol.429
, pp. 274-278
-
-
Sturla, L.1
Etzioni, A.2
Bisso, A.3
-
40
-
-
0025107237
-
Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII
-
Hartsfield JK Jr, Kousseff BG. Phenotypic overlap of Ehlers-Danlos syndrome types IV and VIII. Am J Med Genet 1990;37:465-70.
-
(1990)
Am J Med Genet
, vol.37
, pp. 465-470
-
-
Hartsfield Jr., J.K.1
Kousseff, B.G.2
-
41
-
-
0040920369
-
-
Johns Hopkins University, Baltimore, MD. MIM number: {130080}: {12/8/98}
-
Online Mendelian Inheritance in Man. OMIM™. Johns Hopkins University, Baltimore, MD. MIM number: {130080}: {12/8/98}. World Wide Web URL: http://www.ncbi.nlm.nih.gov/mim/
-
Online Mendelian Inheritance in Man. OMIM™
-
-
-
43
-
-
0032146104
-
Cathepsin C from Schistosoma japonicum - cDNA encoding the preproenzyme and its phylogenetic relationships
-
Hola-Jamriska L, Tort JF, Dalton JP, et al. Cathepsin C from Schistosoma japonicum - cDNA encoding the preproenzyme and its phylogenetic relationships. Eur J Biochem 1998;255:527-34.
-
(1998)
Eur J Biochem
, vol.255
, pp. 527-534
-
-
Hola-Jamriska, L.1
Tort, J.F.2
Dalton, J.P.3
-
44
-
-
0032709548
-
Loss-of-function mutations in the cathepsin c gene result in periodontal disease and palmoplantar keratosis
-
Toomes CJJ, Wood AJ, Wu CL, et al. Loss-of-function mutations in the cathepsin c gene result in periodontal disease and palmoplantar keratosis. Nat Genet 1999;23:421-4.
-
(1999)
Nat Genet
, vol.23
, pp. 421-424
-
-
Toomes, C.J.J.1
Wood, A.J.2
Wu, C.L.3
-
45
-
-
0032774475
-
Clinical spectrum of fibroblast growth factor receptor mutations
-
Passos-Bueno MR, Wilcox WR, Jabs EW, Sertié AL, Alonso LG, Kitoh H. Clinical spectrum of fibroblast growth factor receptor mutations. Hum Mutat 1999;14:115-25.
-
(1999)
Hum Mutat
, vol.14
, pp. 115-125
-
-
Passos-Bueno, M.R.1
Wilcox, W.R.2
Jabs, E.W.3
Sertié, A.L.4
Alonso, L.G.5
Kitoh, H.6
-
46
-
-
0027682822
-
Late onset Papillon-Lefèvre syndrome? A chromosomic, neutrophil function and microbiological study
-
Bullon P, Pascual A, Fernandez-Novoa MC, Borobio MV, Muniain MA, Camacho F. Late onset Papillon-Lefèvre syndrome? A chromosomic, neutrophil function and microbiological study. J Clin Periodontol 1993;20:662-7.
-
(1993)
J Clin Periodontol
, vol.20
, pp. 662-667
-
-
Bullon, P.1
Pascual, A.2
Fernandez-Novoa, M.C.3
Borobio, M.V.4
Muniain, M.A.5
Camacho, F.6
-
47
-
-
0030203497
-
Partial expression of the Papillon-Lefèvre syndrome in 2 unrelated families
-
Soskolne WA, Stabholz A, van Dyke TE, Hart TC, Meyle J. Partial expression of the Papillon-Lefèvre syndrome in 2 unrelated families. J Clin Periodontol 1996;23:764-9.
-
(1996)
J Clin Periodontol
, vol.23
, pp. 764-769
-
-
Soskolne, W.A.1
Stabholz, A.2
Van Dyke, T.E.3
Hart, T.C.4
Meyle, J.5
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