-
1
-
-
0034720855
-
Structural organization of the human NBC1 gene: kNBC1 is transcribed from an alternative promoter in intron 3
-
DOI 10.1016/S0378-1119(00)00204-3, PII S0378111900002043
-
N Abuladze M Song A Pushkin D Newman I Lee S Nicholas I Kurtz 2000 Structural organization of the human NBC1 gene: kNBC1 is transcribed from an alternative promoter in intron 3 Gene 251 109 122 1:CAS:528:DC%2BD3cXktlSlu7s%3D 10.1016/S0378-1119(00)00204-3 10876088 (Pubitemid 30394263)
-
(2000)
Gene
, vol.251
, Issue.2
, pp. 109-122
-
-
Abuladze, N.1
Song, M.2
Pushkin, A.3
Newman, D.4
Lee, I.5
Nicholas, S.6
Kurtz, I.7
-
2
-
-
0027074920
-
Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1)
-
1:CAS:528:DyaK3sXks12ksL8%3D 10.1007/BF00220469 1483698
-
MJ Aldred PJM Crawford E Roberts NST Thomas 1992 Identification of a nonsense mutation in the amelogenin gene (AMELX) in a family with X-linked amelogenesis imperfecta (AIH1) Hum Genet 90 413 416 1:CAS:528:DyaK3sXks12ksL8%3D 10.1007/BF00220469 1483698
-
(1992)
Hum Genet
, vol.90
, pp. 413-416
-
-
Aldred, M.J.1
Crawford, P.J.M.2
Roberts, E.3
Thomas, N.S.T.4
-
3
-
-
0026498777
-
Genetic heterogeneity in X-linked amelogenesis imperfecta
-
1:CAS:528:DyaK3sXhtFOrtL4%3D 10.1016/S0888-7543(05)80153-3 1358807
-
MJ Aldred PJM Crawford E Roberts CM Gillespie NST Thomas I Fenton LA Sandkuijl PS Hart 1992 Genetic heterogeneity in X-linked amelogenesis imperfecta Genomics 14 567 573 1:CAS:528:DyaK3sXhtFOrtL4%3D 10.1016/S0888-7543(05)80153-3 1358807
-
(1992)
Genomics
, vol.14
, pp. 567-573
-
-
Aldred, M.J.1
Crawford, P.J.M.2
Roberts, E.3
Gillespie, C.M.4
Thomas, N.S.T.5
Fenton, I.6
Sandkuijl, L.A.7
Hart, P.S.8
-
4
-
-
0037281187
-
Amelogenesis imperfecta: A classification and catalogue for the 21st century
-
DOI 10.1034/j.1601-0825.2003.00843.x
-
MJ Aldred R Savarirayan PJM Crawford 2003 Amelogenesis imperfecta: a classification and catalogue for the 21st century Oral Dis 9 19 23 1:STN:280:DC%2BD3s7gsVantA%3D%3D 10.1034/j.1601-0825.2003.00843.x 12617253 (Pubitemid 36227694)
-
(2003)
Oral Diseases
, vol.9
, Issue.1
, pp. 19-23
-
-
Aldred, M.J.1
Savarirayan, R.2
Crawford, P.J.M.3
-
5
-
-
0035983870
-
Cystic fibrosis transmembrane regulator gene (CFTR) is associated with abnormal enamel formation
-
1:CAS:528:DC%2BD38Xls1ClsLk%3D 10.1177/154405910208100712 12161463
-
CK Arquitt C Boyd JT Wright 2002 Cystic fibrosis transmembrane regulator gene (CFTR) is associated with abnormal enamel formation J Dent Res 81 492 496 1:CAS:528:DC%2BD38Xls1ClsLk%3D 10.1177/154405910208100712 12161463
-
(2002)
J Dent Res
, vol.81
, pp. 492-496
-
-
Arquitt, C.K.1
Boyd, C.2
Wright, J.T.3
-
6
-
-
0023750395
-
Amelogenesis imperfecta: A genetic study
-
B Bäckman G Holmgren 1988 Amelogenesis imperfecta: a genetic study Hum Hered 38 89 206
-
(1988)
Hum Hered
, vol.38
, pp. 89-206
-
-
Bäckman, B.1
Holmgren, G.2
-
8
-
-
0015348406
-
Hereditary hypocalcified amelogenesis imperfecta. Pedigree analysis
-
1:STN:280:DyaE387ptFyjug%3D%3D 10.1016/0030-4220(72)90183-1 4503458
-
AJ Chabora MD Berkman SL Horowitz HI Nahoum 1972 Hereditary hypocalcified amelogenesis imperfecta. Pedigree analysis Oral Surg Oral Med Oral Pathol 33 922 925 1:STN:280:DyaE387ptFyjug%3D%3D 10.1016/0030-4220(72)90183-1 4503458
-
(1972)
Oral Surg Oral Med Oral Pathol
, vol.33
, pp. 922-925
-
-
Chabora, A.J.1
Berkman, M.D.2
Horowitz, S.L.3
Nahoum, H.I.4
-
9
-
-
0025732652
-
Linkage of amelogenin Amel to the distal portion of the mouse X chromosome
-
1:CAS:528:DyaK3MXks1Grt7c%3D 10.1016/0888-7543(91)90479-X 1675194
-
VM Chapman B Keitz CM Disteche EC Lau ML Snead 1991 Linkage of amelogenin Amel to the distal portion of the mouse X chromosome Genomics 10 23 28 1:CAS:528:DyaK3MXks1Grt7c%3D 10.1016/0888-7543(91)90479-X 1675194
-
(1991)
Genomics
, vol.10
, pp. 23-28
-
-
Chapman, V.M.1
Keitz, B.2
Disteche, C.M.3
Lau, E.C.4
Snead, M.L.5
-
10
-
-
0031106113
-
An amelogenin gene defect associated with human X-linked amelogenesis imperfecta
-
DOI 10.1016/S0003-9969(96)00099-4, PII S0003996996000994
-
PM Collier JJ Sauk J Rosenbloom ZA Yuan CW Gibson 1997 An amelogenin gene defect associated with human X-linked amelogenesis imperfecta Arch Oral Biol 42 235 242 1:CAS:528:DyaK2sXjvFykurg%3D 10.1016/S0003-9969(96)00099-4 9188994 (Pubitemid 27218201)
-
(1997)
Archives of Oral Biology
, vol.42
, Issue.3
, pp. 235-242
-
-
Collier, P.M.1
Sauk, J.J.2
Rosenbloom, J.3
Yuan, Z.A.4
Gibson, C.W.5
-
12
-
-
10844221389
-
A novel missense mutation in the sodium bicarbonate cotransporter (NBCe1/SLC4A4) causes proximal tubular acidosis and glaucoma through ion transport defects
-
DOI 10.1074/jbc.M406591200
-
D Dinour MH Chang J Satoh BL Smith N Angle A Knecht I Serban EJ Holtzman MF Romero 2004 A novel missense mutation in the sodium bicarbonate cotransporter (NBCe1/SLC4A4) causes proximal tubular acidosis and glaucoma through ion transport defects J Biol Chem 279 52238 52246 1:CAS:528:DC%2BD2cXhtVCktbfF 10.1074/jbc.M406591200 15471865 (Pubitemid 39662729)
-
(2004)
Journal of Biological Chemistry
, vol.279
, Issue.50
, pp. 52238-52246
-
-
Dinour, D.1
Chang, M.-H.2
Satoh, J.-I.3
Smith, B.L.4
Angle, N.5
Knecht, A.6
Serban, I.7
Holtzman, E.J.8
Romero, M.F.9
-
14
-
-
0036930739
-
Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate
-
DOI 10.1038/sj.ejhg.5200884
-
ML Downey JT Keen IK Jalili J McHale MJ Aldred SP Robertson 2002 Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregate Eur J Hum Genet 10 865 869 1:CAS:528:DC%2BD38XptFKmtb0%3D 10.1038/sj.ejhg.5200884 12461695 (Pubitemid 36054569)
-
(2002)
European Journal of Human Genetics
, vol.10
, Issue.12
, pp. 865-869
-
-
Downey, L.M.1
Keen, T.J.2
Jalili, I.K.3
McHale, J.4
Aldred, M.J.5
Robertson, S.P.6
Mighell, A.7
Fayle, S.8
Wissinger, B.9
Inglehearn, C.F.10
-
15
-
-
72149121577
-
Mutations in beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta
-
10.1016/j.ajhg.2009.09.014
-
W El-Sayed DA Parry RC Shore M Ahmed H Jafri Y Rashid S Al-Bahlani S Harasi J Kirkham CF Inglehearn AJ Mighell 2009 Mutations in beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta Am J Hum Genet 85 1 7 10.1016/j.ajhg.2009.09.014
-
(2009)
Am J Hum Genet
, vol.85
, pp. 1-7
-
-
El-Sayed, W.1
Parry, D.A.2
Shore, R.C.3
Ahmed, M.4
Jafri, H.5
Rashid, Y.6
Al-Bahlani, S.7
Harasi, S.8
Kirkham, J.9
Inglehearn, C.F.10
Mighell, A.J.11
-
16
-
-
77952310893
-
Ultrastructural analyses of deciduous teeth affected by hypocalcified amelogenesis imperfecta from a family with a novel Y458X FAM83H nonsense mutation
-
1:CAS:528:DC%2BC3cXitlWisLo%3D 10.1159/000252801 20160442
-
W El-Sayed DA Parry RC Shore CF Inglehearn AJ Mighell 2010 Ultrastructural analyses of deciduous teeth affected by hypocalcified amelogenesis imperfecta from a family with a novel Y458X FAM83H nonsense mutation Cells Tissues Organs 191 235 239 1:CAS:528:DC%2BC3cXitlWisLo%3D 10.1159/000252801 20160442
-
(2010)
Cells Tissues Organs
, vol.191
, pp. 235-239
-
-
El-Sayed, W.1
Parry, D.A.2
Shore, R.C.3
Inglehearn, C.F.4
Mighell, A.J.5
-
17
-
-
34247847733
-
- Cotransporter
-
1:CAS:528:DC%2BD2sXivV2mtrc%3D 10.1074/jbc.M607041200 17192275
-
- cotransporter J Biol Chem 282 9042 9052 1:CAS:528:DC%2BD2sXivV2mtrc%3D 10.1074/jbc.M607041200 17192275
-
(2007)
J Biol Chem
, vol.282
, pp. 9042-9052
-
-
Gawenis, L.R.1
Bradford, E.M.2
Prasad, V.3
Lorenz, J.N.4
Simpson, J.E.5
Clarke, L.L.6
Woo, A.L.7
Grisham, C.8
Sanford, L.P.9
Doetschman, T.10
Miller, M.L.11
Shull, G.E.12
-
18
-
-
0015595499
-
A kindred showing hypocalcified amelogenesis imperfecta: Report of case
-
1:STN:280:DyaE3s%2FptVSgtg%3D%3D 4510007
-
JS Giansanti 1973 A kindred showing hypocalcified amelogenesis imperfecta: report of case J Am Dent Assoc 86 675 678 1:STN:280: DyaE3s%2FptVSgtg%3D%3D 4510007
-
(1973)
J Am Dent Assoc
, vol.86
, pp. 675-678
-
-
Giansanti, J.S.1
-
19
-
-
0035943668
-
Amelogenin-deficient mice display an amelogenesis imperfecta phenotype
-
1:CAS:528:DC%2BD3MXms1Smsb8%3D 10.1074/jbc.M104624200 11406633
-
CW Gibson Z Yuan B May G Longenecker E Chen T Thyagarajan T Sreenath JT Wrigt S Decker R Piddington G Harrison AB Kulkarni 2001 Amelogenin-deficient mice display an amelogenesis imperfecta phenotype J Biol Chem 276 31871 31875 1:CAS:528:DC%2BD3MXms1Smsb8%3D 10.1074/jbc.M104624200 11406633
-
(2001)
J Biol Chem
, vol.276
, pp. 31871-31875
-
-
Gibson, C.W.1
Yuan, Z.2
May, B.3
Longenecker, G.4
Chen, E.5
Thyagarajan, T.6
Sreenath, T.7
Wrigt, J.T.8
Decker, S.9
Piddington, R.10
Harrison, G.11
Kulkarni, A.B.12
-
20
-
-
0036008478
-
A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta
-
DOI 10.1016/S0003-9969(01)00111-X, PII S000399690100111X
-
SR Greene ZA Yuan JT Wright H Amjad WR Abrams JA Buchanan DI Trachtenberg CW Gibson 2002 A new frameshift mutation encoding a truncated amelogenin leads to X-linked amelogenesis imperfecta Arch Oral Biol 47 211 217 1:CAS:528:DC%2BD38XhtFylsb4%3D 10.1016/S0003-9969(01)00111-X 11839357 (Pubitemid 34174088)
-
(2002)
Archives of Oral Biology
, vol.47
, Issue.3
, pp. 211-217
-
-
Greene, S.R.1
Yuan, Z.A.2
Wright, J.T.3
Amjad, H.4
Abrams, W.R.5
Buchanan, J.A.6
Trachtenberg, D.I.7
Gibson, C.W.8
-
21
-
-
33947158110
-
Identification of a novel mutation in the enamalin gene in a family with autosomal-dominant amelogenesis imperfecta
-
DOI 10.1016/j.archoralbio.2006.09.014, PII S0003996906002597
-
SJ Gutiérrez M Chaves DM Torres I Briceño 2007 Identification of a novel mutation in the enamelin gene in a family with autosomal-dominant amelogenesis imperfecta Arch Oral Biol 52 503 506 10.1016/j.archoralbio.2006.09.014 17316551 (Pubitemid 46399641)
-
(2007)
Archives of Oral Biology
, vol.52
, Issue.5
, pp. 503-506
-
-
Gutierrez, S.J.1
Chaves, M.2
Torres, D.M.3
Briceno, I.4
-
22
-
-
0033981165
-
Mutational analysis of X-linked amelogenesis imperfecta in multiple families
-
DOI 10.1016/S0003-9969(99)00106-5, PII S0003996999001065
-
S Hart T Hart C Gibson JT Wright 2000 Mutational analysis of X-linked amelogenesis imperfecta in multiple families Arch Oral Biol 45 79 86 1:CAS:528:DyaK1MXnslGmtLo%3D 10.1016/S0003-9969(99)00106-5 10669095 (Pubitemid 30022382)
-
(2000)
Archives of Oral Biology
, vol.45
, Issue.1
, pp. 79-86
-
-
Hart, S.1
Hart, T.2
Gibson, C.3
Wright, J.T.4
-
23
-
-
0036010022
-
Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations
-
DOI 10.1016/S0003-9969(02)00003-1, PII S0003996902000031
-
PS Hart MJ Aldred PJM Crawford NJ Wright TC Hart JT Wright 2002 Amelogenesis imperfecta phenotype-genotype correlations with two amelogenin gene mutations Arch Oral Biol 47 261 265 1:CAS:528:DC%2BD38Xitlalsro%3D 10.1016/S0003-9969(02)00003-1 11922869 (Pubitemid 34292459)
-
(2002)
Archives of Oral Biology
, vol.47
, Issue.4
, pp. 261-265
-
-
Hart, P.S.1
Aldred, M.J.2
Crawford, P.J.M.3
Wright, N.J.4
Hart, T.C.5
Wright, J.T.6
-
24
-
-
0141497179
-
Exclusion of candidate genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta
-
DOI 10.1034/j.1600-0722.2003.00046.x
-
PS Hart JT Wright M Savage JT Bensen MC Gorry TC Hart 2003 Exclusion of candidate of genes in two families with autosomal dominant hypocalcified amelogenesis imperfecta Eur J Oral Sci 111 326 331 1:CAS:528: DC%2BD3sXntFyrsbY%3D 10.1034/j.1600-0722.2003.00046.x 12887398 (Pubitemid 37465501)
-
(2003)
European Journal of Oral Sciences
, vol.111
, Issue.4
, pp. 326-331
-
-
Hart, P.S.1
Wright, J.T.2
Savage, M.3
Kang, G.4
Bensen, J.T.5
Gorry, M.C.6
Hart, T.C.7
-
25
-
-
9144248989
-
Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects
-
1:CAS:528:DC%2BD2cXht1aqsb4%3D 10.1136/jmg.40.12.900 14684688
-
TC Hart PS Hart MC Gorry MD Michalec OH Ryu C Uygur 2003 Novel ENAM mutation responsible for autosomal recessive amelogenesis imperfecta and localised enamel defects J Med Genet 40 900 906 1:CAS:528:DC%2BD2cXht1aqsb4%3D 10.1136/jmg.40.12.900 14684688
-
(2003)
J Med Genet
, vol.40
, pp. 900-906
-
-
Hart, T.C.1
Hart, P.S.2
Gorry, M.C.3
Michalec, M.D.4
Ryu, O.H.5
Uygur, C.6
-
26
-
-
3142773337
-
Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta
-
1:CAS:528:DC%2BD2cXmvVymsbs%3D 10.1136/jmg.2003.017657 15235027
-
PS Hart TC Hart MD Michalec OH Ryu D Simmons S Hong 2004 Mutation in kallikrein 4 causes autosomal recessive hypomaturation amelogenesis imperfecta J Med Genet 41 545 549 1:CAS:528:DC%2BD2cXmvVymsbs%3D 10.1136/jmg.2003.017657 15235027
-
(2004)
J Med Genet
, vol.41
, pp. 545-549
-
-
Hart, P.S.1
Hart, T.C.2
Michalec, M.D.3
Ryu, O.H.4
Simmons, D.5
Hong, S.6
-
27
-
-
65249125086
-
Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta
-
1:CAS:528:DC%2BD1MXmtVOltbg%3D 10.1111/j.1399-0004.2008.01112.x 19220331
-
PS Hart S Becerik D Cogulu G Emingil D Ozdemir-Ozenen ST Han PP Sulima E Firatli TC Hart 2009 Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta Clin Genet 75 401 404 1:CAS:528:DC%2BD1MXmtVOltbg%3D 10.1111/j.1399-0004.2008.01112.x 19220331
-
(2009)
Clin Genet
, vol.75
, pp. 401-404
-
-
Hart, P.S.1
Becerik, S.2
Cogulu, D.3
Emingil, G.4
Ozdemir-Ozenen, D.5
Han, S.T.6
Sulima, P.P.7
Firatli, E.8
Hart, T.C.9
-
28
-
-
70349850806
-
Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta
-
10.1111/j.1365-2591.2009.01617.x 19825039
-
HK Hyun SK Lee KE Lee HY Kang EJ Kim PH Choung JW Kim 2009 Identification of a novel FAM83H mutation and microhardness of an affected molar in autosomal dominant hypocalcified amelogenesis imperfecta Int Endod J 42 1039 1043 10.1111/j.1365-2591.2009.01617.x 19825039
-
(2009)
Int Endod J
, vol.42
, pp. 1039-1043
-
-
Hyun, H.K.1
Lee, S.K.2
Lee, K.E.3
Kang, H.Y.4
Kim, E.J.5
Choung, P.H.6
Kim, J.W.7
-
29
-
-
3442880476
-
Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis
-
1:CAS:528:DC%2BD2cXltVSnu7c%3D 10.1007/s00424-004-1278-1 15085340
-
J Inatomi S Horita N Braverman T Sekine H Yamada Y Suzuki K Kawahara N Moriyama A Kudo H Kawakami M Shimadzu H Endou T Fujita G Seki T Igarashi 2004 Mutational and functional analysis of SLC4A4 in a patient with proximal renal tubular acidosis Pflugers Arch 448 438 444 1:CAS:528:DC%2BD2cXltVSnu7c%3D 10.1007/s00424-004-1278-1 15085340
-
(2004)
Pflugers Arch
, vol.448
, pp. 438-444
-
-
Inatomi, J.1
Horita, S.2
Braverman, N.3
Sekine, T.4
Yamada, H.5
Suzuki, Y.6
Kawahara, K.7
Moriyama, N.8
Kudo, A.9
Kawakami, H.10
Shimadzu, M.11
Endou, H.12
Fujita, T.13
Seki, G.14
Igarashi, T.15
-
30
-
-
65349093351
-
Candidate gene strategy reveals ENAM mutations
-
1:CAS:528:DC%2BD1MXltVOiu7Y%3D 19329462
-
HY Kang F Seymen SK Lee M Yildirim E Bahar Tuna A Patir KE Lee JW Kim 2009 Candidate gene strategy reveals ENAM mutations J Dent Res 88 266 269 1:CAS:528:DC%2BD1MXltVOiu7Y%3D 19329462
-
(2009)
J Dent Res
, vol.88
, pp. 266-269
-
-
Kang, H.Y.1
Seymen, F.2
Lee, S.K.3
Yildirim, M.4
Bahar Tuna, E.5
Patir, A.6
Lee, K.E.7
Kim, J.W.8
-
31
-
-
0036827621
-
Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation al the exon-intron boundary
-
1:CAS:528:DC%2BD38XovFKmsrw%3D 10.1177/154405910208101103 12407086
-
M Kida T Ariga T Shirakawa H Oguchi Y Sakiyama 2002 Autosomal-dominant hypoplastic form of amelogenesis imperfecta caused by an enamelin gene mutation al the exon-intron boundary J Dent Res 81 738 742 1:CAS:528:DC%2BD38XovFKmsrw%3D 10.1177/154405910208101103 12407086
-
(2002)
J Dent Res
, vol.81
, pp. 738-742
-
-
Kida, M.1
Ariga, T.2
Shirakawa, T.3
Oguchi, H.4
Sakiyama, Y.5
-
32
-
-
33846546178
-
A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta
-
1:CAS:528:DC%2BD2sXhsV2ltLs%3D 10.1177/154405910708600111 17189466
-
M Kida Y Sakiyama A Matsuda S Takabayashi H Ochi H Sekiguchi S Minamitake T Ariga 2007 A novel missense mutation (p.P52R) in amelogenin gene causing X-linked amelogenesis imperfecta J Dent Res 86 69 72 1:CAS:528: DC%2BD2sXhsV2ltLs%3D 10.1177/154405910708600111 17189466
-
(2007)
J Dent Res
, vol.86
, pp. 69-72
-
-
Kida, M.1
Sakiyama, Y.2
Matsuda, A.3
Takabayashi, S.4
Ochi, H.5
Sekiguchi, H.6
Minamitake, S.7
Ariga, T.8
-
33
-
-
2442666831
-
Amelogenin p.M1T and p.W4S mutations underlaying hypoplastic X-linked amelogenesis imperfecta
-
1:CAS:528:DC%2BD2cXktlKitbg%3D 10.1177/154405910408300505 15111628
-
JW Kim JP Simmer YY Hu BPL Lin C Boyd JT Wright CJM Yamada SK Rayes RJ Feirgal JCC Hu 2004 Amelogenin p.M1T and p.W4S mutations underlaying hypoplastic X-linked amelogenesis imperfecta J Dent Res 83 378 383 1:CAS:528: DC%2BD2cXktlKitbg%3D 10.1177/154405910408300505 15111628
-
(2004)
J Dent Res
, vol.83
, pp. 378-383
-
-
Kim, J.W.1
Simmer, J.P.2
Hu, Y.Y.3
Lin, B.P.L.4
Boyd, C.5
Wright, J.T.6
Yamada, C.J.M.7
Rayes, S.K.8
Feirgal, R.J.9
Hu, J.C.C.10
-
34
-
-
16844370307
-
ENAM mutations in autosomal-dominant amelogenesis imperfecta
-
DOI 10.1177/154405910508400314
-
JW Kim F Seymen BPJ Lin B Kiziltan K Gencay JP Simmer 2005 ENAM mutations in autosomal dominant amelogenesis imperfecta J Dent Res 84 278 282 1:CAS:528:DC%2BD2MXis1Wlurk%3D 10.1177/154405910508400314 15723871 (Pubitemid 43822038)
-
(2005)
Journal of Dental Research
, vol.84
, Issue.3
, pp. 278-282
-
-
Kim, J.-W.1
Seymen, F.2
Lin, B.P.-J.3
Kiziltan, B.4
Gencay, K.5
Simmer, J.P.6
Hu, J.C.-C.7
-
35
-
-
15044355868
-
MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta
-
DOI 10.1136/jmg.2004.024505
-
JW Kim JP Simmer TC Hart PS Hart MD Ramaswami JD Bartlett 2005 MMP-20 mutation in autosomal recessive pigmented hypomaturation amelogenesis imperfecta J Med Genet 42 271 275 1:CAS:528:DC%2BD2MXjtVertrs%3D 10.1136/jmg.2004.024505 15744043 (Pubitemid 40380310)
-
(2005)
Journal of Medical Genetics
, vol.42
, Issue.3
, pp. 271-275
-
-
Kim, J.-W.1
Simmer, J.P.2
Hart, T.C.3
Hart, P.S.4
Ramaswami, M.D.5
Bartlett, J.D.6
Hu, J.C.-C.7
-
36
-
-
33646529339
-
Mutational analysis of candidate genes in 24 amelogenesis imperfecta families
-
DOI 10.1111/j.1600-0722.2006.00278.x
-
JW Kim JP Simmer BPL Lin F Seymen JD Bartlett JCC Hu 2006 Mutational analysis of candidate genes in 24 amelogenesis imperfect families Eur J Oral Sci 114 Suppl 1 3 12 1:CAS:528:DC%2BD28XlvF2hurs%3D 10.1111/j.1600-0722.2006.00278. x 16674655 (Pubitemid 43709407)
-
(2006)
European Journal of Oral Sciences
, vol.114
, Issue.SUPPL. 1
, pp. 3-12
-
-
Kim, J.-W.1
Simmer, J.P.2
Lin, B.P.-L.3
Seymen, F.4
Bartlett, J.D.5
Hu, J.C.-C.6
-
37
-
-
40749109023
-
FAM83H Mutations in Families with Autosomal-Dominant Hypocalcified Amelogenesis Imperfecta
-
DOI 10.1016/j.ajhg.2007.09.020, PII S000292970800075X
-
JW Kim SK Lee ZH Lee JC Park KE Lee MH Lee JT Park 2008 FAM83H mutations in families with autosomal dominant hypocalcified amelogenesis imperfect Am J Hum Genet 82 489 494 1:CAS:528:DC%2BD1cXit1Sisrg%3D 10.1016/j.ajhg.2007.09.020 18252228 (Pubitemid 351726098)
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.2
, pp. 489-494
-
-
Kim, J.-W.1
Lee, S.-K.2
Lee, Z.H.3
Park, J.-C.4
Lee, K.-E.5
Lee, M.-H.6
Park, J.-T.7
Seo, B.-M.8
Hu, J.C.-C.9
Simmer, J.P.10
-
38
-
-
0034445110
-
Detection of a novel mutation in X-linked amelogenesis imperfecta
-
1:CAS:528:DC%2BD3MXptVKmsA%3D%3D 10.1177/00220345000790120901 11201048
-
SA Kindelan AH Brook L Gangemi N Lench FSL Wong J Fearne Z Jackson G Foster BMJ Stringer 2000 Detection of a novel mutation in X-linked amelogenesis imperfecta J Dent Res 79 1978 1982 1:CAS:528:DC%2BD3MXptVKmsA%3D%3D 10.1177/00220345000790120901 11201048
-
(2000)
J Dent Res
, vol.79
, pp. 1978-1982
-
-
Kindelan, S.A.1
Brook, A.H.2
Gangemi, L.3
Lench, N.4
Wong, F.S.L.5
Fearne, J.6
Jackson, Z.7
Foster, G.8
Stringer, B.M.J.9
-
40
-
-
0025740360
-
A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1)
-
10.1016/0888-7543(91)90187-J 1916828
-
M Lagerström N Dhal Y Nakahori Y Makagome B Bäckman U Landegren U Pettersson 1991 A deletion in the amelogenin gene (AMG) causes X-linked amelogenesis imperfecta (AIH1) Genomics 10 971 975 10.1016/0888-7543(91)90187-J 1916828
-
(1991)
Genomics
, vol.10
, pp. 971-975
-
-
Lagerström, M.1
Dhal, N.2
Nakahori, Y.3
Makagome, Y.4
Bäckman, B.5
Landegren, U.6
Pettersson, U.7
-
41
-
-
0028921003
-
Amelogenin signal peptide mutation: Correlation between mutation in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta
-
10.1016/0888-7543(95)80097-6 7782077
-
M Lagerström-Fermér M Nilsson B Bäckman E Salido LJ Shapiro U Pettersson U Landegren 1995 Amelogenin signal peptide mutation: Correlation between mutation in the amelogenin gene (AMGX) and manifestations of X-linked amelogenesis imperfecta Genomics 26 159 162 10.1016/0888-7543(95) 80097-6 7782077
-
(1995)
Genomics
, vol.26
, pp. 159-162
-
-
Lagerström-Fermér, M.1
Nilsson, M.2
Bäckman, B.3
Salido, E.4
Shapiro, L.J.5
Pettersson, U.6
Landegren, U.7
-
42
-
-
65249169172
-
Mutational spectrum of FAM83H: The C-terminal portion is required for tooth enamel calcification
-
10.1002/humu.20789 18484629
-
SK Lee JC Hu JD Bartlett KE Lee BPJ Lin JP Simmer JW Kim 2008 Mutational spectrum of FAM83H: the C-terminal portion is required for tooth enamel calcification Hum Mutat 29 E95 E99 10.1002/humu.20789 18484629
-
(2008)
Hum Mutat
, vol.29
-
-
Lee, S.K.1
Hu, J.C.2
Bartlett, J.D.3
Lee, K.E.4
Lin, B.P.J.5
Simmer, J.P.6
Kim, J.W.7
-
43
-
-
42449137084
-
DLX3 mutation in a new family and its phenotypic variations
-
1:CAS:528:DC%2BD1cXltVKgs74%3D 10.1177/154405910808700402 18362318
-
SK Lee ZH Lee SJ Lee BD Ahn YJ Kim SH Lee JW Kim 2008 DLX3 mutation in a new family and its phenotypic variations J Dent Res 87 354 357 1:CAS:528:DC%2BD1cXltVKgs74%3D 10.1177/154405910808700402 18362318
-
(2008)
J Dent Res
, vol.87
, pp. 354-357
-
-
Lee, S.K.1
Lee, Z.H.2
Lee, S.J.3
Ahn, B.D.4
Kim, Y.J.5
Lee, S.H.6
Kim, J.W.7
-
44
-
-
72449203350
-
MMP-20 hemopexina domain mutation in amelogenesis imperfecta
-
1:CAS:528:DC%2BC3cXhtFOks7g%3D 10.1177/0022034509352844 19966041
-
SK Lee F Seymen HY Kang KE Lee B Gencay B Tuna JW Kim 2010 MMP-20 hemopexina domain mutation in amelogenesis imperfecta J Dent Res 89 46 50 1:CAS:528:DC%2BC3cXhtFOks7g%3D 10.1177/0022034509352844 19966041
-
(2010)
J Dent Res
, vol.89
, pp. 46-50
-
-
Lee, S.K.1
Seymen, F.2
Kang, H.Y.3
Lee, K.E.4
Gencay, B.5
Tuna, B.6
Kim, J.W.7
-
45
-
-
0028947327
-
Characterization of molecular defects in X-linked amelogenesis imperfecta (AIH1)
-
1:CAS:528:DyaK2MXlt1ertr8%3D 10.1002/humu.1380050310 7599636
-
NJ Lench GB Winter 1995 Characterization of molecular defects in X-linked amelogenesis imperfecta (AIH1) Hum Mutat 5 251 259 1:CAS:528:DyaK2MXlt1ertr8%3D 10.1002/humu.1380050310 7599636
-
(1995)
Hum Mutat
, vol.5
, pp. 251-259
-
-
Lench, N.J.1
Winter, G.B.2
-
46
-
-
0028223018
-
SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1)
-
1:CAS:528:DyaK2cXksFGiur8%3D 10.1093/hmg/3.5.827 8081371
-
NJ Lench AH Brook GB Winter 1994 SSCP detection of a nonsense mutation in exon 5 of the amelogenin gene (AMGX) causing X-linked amelogenesis imperfecta (AIH1) Hum Mol Genet 3 827 828 1:CAS:528:DyaK2cXksFGiur8%3D 10.1093/hmg/3.5.827 8081371
-
(1994)
Hum Mol Genet
, vol.3
, pp. 827-828
-
-
Lench, N.J.1
Brook, A.H.2
Winter, G.B.3
-
48
-
-
38949209872
-
The anion exchanger Ae2 is required for enamel maturation in mouse teeth
-
DOI 10.1016/j.matbio.2007.09.006, PII S0945053X07001138
-
DM Lyaruu AL Bronckers L Mulder P Mardones JF Medina S Kellokumpu RP Oude Elferink V Everts 2008 The anion exchanger Ae2 is required for enamel maturation in mouse teeth Matrix Biol 27 119 127 1:CAS:528:DC%2BD1cXhvVWitLc%3D 10.1016/j.matbio.2007.09.006 18042363 (Pubitemid 351227380)
-
(2008)
Matrix Biology
, vol.27
, Issue.2
, pp. 119-127
-
-
Lyaruu, D.M.1
Bronckers, A.L.J.J.2
Mulder, L.3
Mardones, P.4
Medina, J.F.5
Kellokumpu, S.6
Oude Elferink, R.P.J.7
Everts, V.8
-
49
-
-
0036566265
-
A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2)
-
1:CAS:528:DC%2BD38XjvFSntb8%3D 10.1093/hmg/11.9.1069 11978766
-
CK Mardh B Bäckman G Holmgren JCC Hu JP Simmer K Forsman-Semb 2002 A nonsense mutation in the enamelin gene causes local hypoplastic autosomal dominant amelogenesis imperfecta (AIH2) Hum Mol Genet 11 1069 1074 1:CAS:528:DC%2BD38XjvFSntb8%3D 10.1093/hmg/11.9.1069 11978766
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1069-1074
-
-
Mardh, C.K.1
Bäckman, B.2
Holmgren, G.3
Hu, J.C.C.4
Simmer, J.P.5
Forsman-Semb, K.6
-
50
-
-
33845611155
-
A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q24.3
-
DOI 10.1007/s00439-006-0246-6
-
G Mendoza TJ Pemberton K Lee R Scarel-Caminaga RM Shai C Gonzalez-Quevedo 2007 A new locus for autosomal dominant amelogenesis imperfecta on chromosome 8q243 Hum Genet 120 653 662 1:CAS:528:DC%2BD28XhtlCjtrjL 10.1007/s00439-006- 0246-6 17024372 (Pubitemid 44942849)
-
(2007)
Human Genetics
, vol.120
, Issue.5
, pp. 653-662
-
-
Mendoza, G.1
Pemberton, T.J.2
Lee, K.3
Scarel-Caminaga, R.4
Mehrian-Shai, R.5
Gonzalez-Quevedo, C.6
Ninis, V.7
Hartiala, J.8
Allayee, H.9
Snead, M.L.10
Leal, S.M.11
Line, S.R.P.12
Patel, P.I.13
-
51
-
-
2942731424
-
An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta
-
1:CAS:528:DC%2BD2cXlsl2gsbk%3D 10.1136/jmg.2003.015792 15173235
-
M Michaelides A Bloch-Zupan GE Holder DM Hunt AT Moore 2004 An autosomal recessive cone-rod dystrophy associated with amelogenesis imperfecta J Med Genet 41 468 473 1:CAS:528:DC%2BD2cXlsl2gsbk%3D 10.1136/jmg.2003.015792 15173235
-
(2004)
J Med Genet
, vol.41
, pp. 468-473
-
-
Michaelides, M.1
Bloch-Zupan, A.2
Holder, G.E.3
Hunt, D.M.4
Moore, A.T.5
-
52
-
-
0003713446
-
-
W B Saunders Co Philadelphia
-
Neville B, Damm D, Allen C, Bouquot J (1995) Oral and maxillofacial pathology. W B Saunders Co, Philadelphia, pp 374-376
-
(1995)
Oral and Maxillofacial Pathology
, pp. 374-376
-
-
Neville, B.1
Damm, D.2
Allen, C.3
Bouquot, J.4
-
54
-
-
33644652965
-
MMP20 active-site mutation in hypomaturation amelogenesis imperfecta
-
DOI 10.1177/154405910508401112
-
D Ozdemir PS Hart OH Ryu SJ Choi M Ozdemir-Karatas E Firatli 2005 MMP20 active-site mutation in hypomaturation amelogenesis imperfecta J Dent Res 84 1031 1035 1:CAS:528:DC%2BD2MXht1Git73N 10.1177/154405910508401112 16246936 (Pubitemid 43828151)
-
(2005)
Journal of Dental Research
, vol.84
, Issue.11
, pp. 1031-1035
-
-
Ozdemir, D.1
Hart, P.S.2
Ryu, O.H.3
Choi, S.J.4
Ozdemir-Karatas, M.5
Firatli, E.6
Piesco, N.7
Hart, T.C.8
-
55
-
-
42449157194
-
Role of NBCe1 and AE2 in secretory ameloblasts
-
1:CAS:528:DC%2BD1cXltVKgs7s%3D 10.1177/154405910808700415 18362326
-
ML Paine ML Snead HJ Wang N Abuladze A Pushkin W Liu LY Kao SM Wall YH Kim I Kurtz 2008 Role of NBCe1 and AE2 in secretory ameloblasts J Dent Res 87 391 395 1:CAS:528:DC%2BD1cXltVKgs7s%3D 10.1177/154405910808700415 18362326
-
(2008)
J Dent Res
, vol.87
, pp. 391-395
-
-
Paine, M.L.1
Snead, M.L.2
Wang, H.J.3
Abuladze, N.4
Pushkin, A.5
Liu, W.6
Kao, L.Y.7
Wall, S.M.8
Kim, Y.H.9
Kurtz, I.10
-
56
-
-
38149007267
-
Premature stop codon in MMP-20 causing amelogenesis imperfecta
-
1:CAS:528:DC%2BD1cXhtFKmtb4%3D 10.1177/154405910808700109 18096894
-
P Papagerakis HK Lin KY Lee Y Hu JP Simmer JD Bartlett JC Hu 2008 Premature stop codon in MMP-20 causing amelogenesis imperfecta J Dent Res 87 56 59 1:CAS:528:DC%2BD1cXhtFKmtb4%3D 10.1177/154405910808700109 18096894
-
(2008)
J Dent Res
, vol.87
, pp. 56-59
-
-
Papagerakis, P.1
Lin, H.K.2
Lee, K.Y.3
Hu, Y.4
Simmer, J.P.5
Bartlett, J.D.6
Hu, J.C.7
-
57
-
-
34250164284
-
Severely hypoplastic amelogenesis imperfecta with taurodontism
-
10.1111/j.1365-263X.2007.00827.x 17559453
-
A Pavlic PL Lukinmaa P Nieminen A Kiukkonen S Alaluusua 2007 Severely hypoplastic amelogenesis imperfecta with taurodontism Int J Paediatr Dent 17 259 266 10.1111/j.1365-263X.2007.00827.x 17559453
-
(2007)
Int J Paediatr Dent
, vol.17
, pp. 259-266
-
-
Pavlic, A.1
Lukinmaa, P.L.2
Nieminen, P.3
Kiukkonen, A.4
Alaluusua, S.5
-
58
-
-
33645581428
-
2-) transporters: Classification, function, structure, genetic diseases, and knockout models
-
DOI 10.1152/ajprenal.00252.2005
-
-2 ) transporters: classification, function, structure, genetic diseases, and knockout models Am J Physiol Renal Physiol 290 F580 F599 1:CAS:528:DC%2BD28XjtFCnsbw%3D 10.1152/ajprenal.00252.2005 16461757 (Pubitemid 43724958)
-
(2006)
American Journal of Physiology - Renal Physiology
, vol.290
, Issue.3
-
-
Pushkin, A.1
Kurtz, I.2
-
59
-
-
0035422249
-
Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta
-
1:CAS:528:DC%2BD3MXmtFagtrg%3D 10.1093/hmg/10.16.1673 11487571
-
MH Rajpar K Harley C Laing RM Davies MJ Dixon 2001 Mutation of the gene encoding the enamel-specific protein, enamelin, causes autosomal-dominant amelogenesis imperfecta Hum Mol Genet 10 1673 1677 1:CAS:528: DC%2BD3MXmtFagtrg%3D 10.1093/hmg/10.16.1673 11487571
-
(2001)
Hum Mol Genet
, vol.10
, pp. 1673-1677
-
-
Rajpar, M.H.1
Harley, K.2
Laing, C.3
Davies, R.M.4
Dixon, M.J.5
-
60
-
-
0034444658
-
Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation
-
1:STN:280:DC%2BD3Mvos1yksg%3D%3D 10.1177/00220345000790070801 11005731
-
DB Ravassipour PS Hart TC Hart AV Ritter M Yamauchi C Gibson JT Wrigth 2000 Unique enamel phenotype associated with amelogenin gene (AMELX) codon 41 point mutation J Dent Res 79 1476 1481 1:STN:280:DC%2BD3Mvos1yksg%3D%3D 10.1177/00220345000790070801 11005731
-
(2000)
J Dent Res
, vol.79
, pp. 1476-1481
-
-
Ravassipour, D.B.1
Hart, P.S.2
Hart, T.C.3
Ritter, A.V.4
Yamauchi, M.5
Gibson, C.6
Wrigth, J.T.7
-
61
-
-
34247857785
-
Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta
-
10.1186/1746-160X-3-8 17266769
-
M Santos PS Hart M Ramaswami C Kanno TC Hart S Line 2007 Exclusion of known gene for enamel development in two Brazilian families with amelogenesis imperfecta Head Face Med 3 8 15 10.1186/1746-160X-3-8 17266769
-
(2007)
Head Face Med
, vol.3
, pp. 8-15
-
-
Santos, M.1
Hart, P.S.2
Ramaswami, M.3
Kanno, C.4
Hart, T.C.5
Line, S.6
-
63
-
-
0015338196
-
Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta
-
4623931
-
JJ Sauk HW Lyon CJ Witkop 1972 Electron optic microanalysis of two gene products in enamel of females heterozygous for X-linked hypomaturation amelogenesis imperfecta Am J Hum Genet 24 267 276 4623931
-
(1972)
Am J Hum Genet
, vol.24
, pp. 267-276
-
-
Sauk, J.J.1
Lyon, H.W.2
Witkop, C.J.3
-
64
-
-
0000823621
-
DNA diagnosis of X-linked amelogenesis imperfecta using PCR detection method of the human amelogenin gene
-
H Sekiguchi M Kiyoshi M Yakushiiji 2001 DNA diagnosis of X-linked amelogenesis imperfecta using PCR detection method of the human amelogenin gene Dent Jpn 37 109 112
-
(2001)
Dent Jpn
, vol.37
, pp. 109-112
-
-
Sekiguchi, H.1
Kiyoshi, M.2
Yakushiiji, M.3
-
65
-
-
0029079604
-
Molecular mechanism of dental enamel formation
-
1:STN:280:DyaK28%2FlsF2hsQ%3D%3D 10.1177/10454411950060020701 7548623
-
JP Simmer AG Fincham 1995 Molecular mechanism of dental enamel formation Crit Rev Oral Biol Med 6 84 108 1:STN:280:DyaK28%2FlsF2hsQ%3D%3D 10.1177/10454411950060020701 7548623
-
(1995)
Crit Rev Oral Biol Med
, vol.6
, pp. 84-108
-
-
Simmer, J.P.1
Fincham, A.G.2
-
66
-
-
12544256630
-
Mineral acquisition rates in developing enamel on maxillary and mandibular incisors of rats and mice: Implications to extracellular acid loading as apatite crystals mature
-
1:CAS:528:DC%2BD2MXhsFarsrs%3D 10.1359/JBMR.041002 15647818
-
CE Smith DL Chong JD Bartlett HC Margolis 2005 Mineral acquisition rates in developing enamel on maxillary and mandibular incisors of rats and mice: implications to extracellular acid loading as apatite crystals mature J Bone Miner Res 20 240 249 1:CAS:528:DC%2BD2MXhsFarsrs%3D 10.1359/JBMR.041002 15647818
-
(2005)
J Bone Miner Res
, vol.20
, pp. 240-249
-
-
Smith, C.E.1
Chong, D.L.2
Bartlett, J.D.3
Margolis, H.C.4
-
67
-
-
33644788720
-
Genes and related proteins involved in amelogenesis imperfecta
-
DOI 10.1177/154405910508401206
-
G Stephanopoulos ME Garefalaki K Lyroudia 2005 Genes and related proteins involved in amelogenesis imperfecta J Dent Res 84 1117 1126 1:CAS:528:DC%2BD28Xps1arsA%3D%3D 10.1177/154405910508401206 16304440 (Pubitemid 43827778)
-
(2005)
Journal of Dental Research
, vol.84
, Issue.12
, pp. 1117-1126
-
-
Stephanopoulos, G.1
Garefalaki, M.-E.2
Lyroudia, K.3
-
68
-
-
0038388765
-
Altered pH regulation during enamel development in the cystic fibrosis mouse incisor
-
1:CAS:528:DC%2BD3sXjvVSgurw%3D 10.1177/154405910308200512 12709507
-
W Sui C Boyd JT Wright 2003 Altered pH regulation during enamel development in the cystic fibrosis mouse incisor J Dent Res 82 388 392 1:CAS:528:DC%2BD3sXjvVSgurw%3D 10.1177/154405910308200512 12709507
-
(2003)
J Dent Res
, vol.82
, pp. 388-392
-
-
Sui, W.1
Boyd, C.2
Wright, J.T.3
-
70
-
-
0018728201
-
Congenital persistent proximal type renal tubular acidosis in two brothers
-
1:STN:280:DyaL3c7ltVWgsw%3D%3D 10.1111/j.1651-2227.1979.tb08224.x 44068
-
A Winsnes E Monn O Stokke T Feyling 1979 Congenital persistent proximal type renal tubular acidosis in two brothers Acta Paediatr Scand 68 861 868 1:STN:280:DyaL3c7ltVWgsw%3D%3D 10.1111/j.1651-2227.1979.tb08224.x 44068
-
(1979)
Acta Paediatr Scand
, vol.68
, pp. 861-868
-
-
Winsnes, A.1
Monn, E.2
Stokke, O.3
Feyling, T.4
-
71
-
-
0024117250
-
Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: Problems in classification
-
10.1111/j.1600-0714.1988.tb01332.x
-
CJ Witkop 1989 Amelogenesis imperfecta, dentinogenesis imperfecta and dentin dysplasia revisited: problems in classification J Oral Pathol 17 547 553 10.1111/j.1600-0714.1988.tb01332.x
-
(1989)
J Oral Pathol
, vol.17
, pp. 547-553
-
-
Witkop, C.J.1
-
72
-
-
33845277788
-
The molecular etiologies and associated phenotypes of amelogenesis imperfecta
-
16838342
-
JT Wright 2006 The molecular etiologies and associated phenotypes of amelogenesis imperfecta Am J Med Genet A 140 2547 2555 16838342
-
(2006)
Am J Med Genet A
, vol.140
, pp. 2547-2555
-
-
Wright, J.T.1
-
75
-
-
0030632370
-
The protein composition of normal and developmentally defective enamel
-
D.J. Chadwick G. Cardew (eds). Wiley Chichester
-
Wright JT, Hall K, Yamauchi M (1997) The protein composition of normal and developmentally defective enamel. In: Chadwick DJ, Cardew G (eds) Dental enamel. Wiley, Chichester, pp 85-106
-
(1997)
Dental Enamel
, pp. 85-106
-
-
Wright, J.T.1
Hall, K.2
Yamauchi, M.3
-
76
-
-
12244272406
-
Relationship of phenotype and genotype in X-linked amelogenesis imperfecta
-
1:CAS:528:DC%2BD3sXjtlamsLk%3D 12952177
-
JT Wright PS Hart MJ Aldred K Seow PJM Crawford SP Hong CW Gibson TC Hart 2003 Relationship of phenotype and genotype in X-linked amelogenesis imperfecta Connect Tissue Res 44 Suppl 1 72 78 1:CAS:528:DC%2BD3sXjtlamsLk%3D 12952177
-
(2003)
Connect Tissue Res
, vol.44
, Issue.SUPPL. 1
, pp. 72-78
-
-
Wright, J.T.1
Hart, P.S.2
Aldred, M.J.3
Seow, K.4
Crawford, P.J.M.5
Hong, S.P.6
Gibson, C.W.7
Hart, T.C.8
-
78
-
-
66149136519
-
Phenotypic variations in FAM83H-associated amelogenesis imperfecta
-
1:CAS:528:DC%2BD1MXmtlantbc%3D 10.1177/0022034509333822 19407157
-
JT Wright S Frazier-Bowers D Simmons K Alexander P Crawford ST Han PS Hart TC Hart 2009 Phenotypic variations in FAM83H-associated amelogenesis imperfecta J Dent Res 88 356 360 1:CAS:528:DC%2BD1MXmtlantbc%3D 10.1177/0022034509333822 19407157
-
(2009)
J Dent Res
, vol.88
, pp. 356-360
-
-
Wright, J.T.1
Frazier-Bowers, S.2
Simmons, D.3
Alexander, K.4
Crawford, P.5
Han, S.T.6
Hart, P.S.7
Hart, T.C.8
|