-
1
-
-
0025922703
-
G protein Gs-alpha (GNAS1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2
-
Gopal Rao VVN, Schnittger S, Hansmann I. 1991. G protein Gs-alpha (GNAS1), the probable candidate gene for Albright hereditary osteodystrophy, is assigned to human chromosome 20q12-q13.2. Genomics 10:257-261.
-
(1991)
Genomics
, vol.10
, pp. 257-261
-
-
Gopal Rao, V.V.N.1
Schnittger, S.2
Hansmann, I.3
-
2
-
-
0014307514
-
Brachydactyly and pseudo-pseudohypoparathyroidism
-
Hertzog KP. 1968. Brachydactyly and pseudo-pseudohypoparathyroidism. Acta Genet Med Gemellol 17:428-437.
-
(1968)
Acta Genet Med Gemellol
, vol.17
, pp. 428-437
-
-
Hertzog, K.P.1
-
3
-
-
33646215618
-
Deletion of GPR35 gene on 2q37.3 may account for Albright hereditary osteodystrophy like phenotype: Defining further genetic variants within and around GPR35 gene
-
Hoo JJ, Shrimpton AE, Braddock BR, Thomson LL, Stein CS. 2003. Deletion of GPR35 gene on 2q37.3 may account for Albright hereditary osteodystrophy like phenotype: Defining further genetic variants within and around GPR35 gene. Am J Hum Genet 73:A653.
-
(2003)
Am J Hum Genet
, vol.73
-
-
Hoo, J.J.1
Shrimpton, A.E.2
Braddock, B.R.3
Thomson, L.L.4
Stein, C.S.5
-
4
-
-
0037383834
-
Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E
-
Johnson D, Kan S, Oldridge M, Trembath RC, Roche P, Esnouf RM, Giele H, Wilkie AOM. 2003. Missense mutations in the homeodomain of HOXD13 are associated with brachydactyly types D and E. Am J Hum Genet 72:984-997.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 984-997
-
-
Johnson, D.1
Kan, S.2
Oldridge, M.3
Trembath, R.C.4
Roche, P.5
Esnouf, R.M.6
Giele, H.7
Wilkie, A.O.M.8
-
7
-
-
0029080844
-
Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals
-
Phelan MC, Rogers RC, Clarkson KB, Bowyer FP, Levine MA, Estabrooks LL, Severson MC, Dobyns WB. 1995. Albright hereditary osteodystrophy and del(2)(q37.3) in four unrelated individuals. Am J Med Genet 58:1-7.
-
(1995)
Am J Med Genet
, vol.58
, pp. 1-7
-
-
Phelan, M.C.1
Rogers, R.C.2
Clarkson, K.B.3
Bowyer, F.P.4
Levine, M.A.5
Estabrooks, L.L.6
Severson, M.C.7
Dobyns, W.B.8
-
8
-
-
0021854061
-
A new brachydactyly syndrome with similarities to Julia Bell types B and E
-
Pitt P, Williams I. 1985. A new brachydactyly syndrome with similarities to Julia Bell types B and E. J Med Genet 22:202-204.
-
(1985)
J Med Genet
, vol.22
, pp. 202-204
-
-
Pitt, P.1
Williams, I.2
-
9
-
-
0030916590
-
RDCI, the vasoactive intestinal peptide receptor: A candidate gene for the features of Albright hereditary osteodystrophy associated with deletion 2q37
-
Power MM, James RS, Barber JCK, Fisher AM, Wood PJ, Leatherdale BA, Flanagan DEH, Hatchwell E. 1997. RDCI, the vasoactive intestinal peptide receptor: A candidate gene for the features of Albright hereditary osteodystrophy associated with deletion 2q37. J Med Genet 34:287-290.
-
(1997)
J Med Genet
, vol.34
, pp. 287-290
-
-
Power, M.M.1
James, R.S.2
Barber, J.C.K.3
Fisher, A.M.4
Wood, P.J.5
Leatherdale, B.A.6
Flanagan, D.E.H.7
Hatchwell, E.8
-
11
-
-
0028813978
-
Brachydactyly and mental retardation: An Albright hereditary osteodystrophy-like syndrome localized to 2q37
-
Wilson LC, Leverton K, Oude Luttikhuis MEM, Oley CA, Flint J, Wolstenholme J, Duckett DP, Barrow MA, Leonard JV, Read AP, Trembath RC. 1995. Brachydactyly and mental retardation: An Albright hereditary osteodystrophy-like syndrome localized to 2q37. Am J Hum Genet 56:400-407.
-
(1995)
Am J Hum Genet
, vol.56
, pp. 400-407
-
-
Wilson, L.C.1
Leverton, K.2
Oude Luttikhuis, M.E.M.3
Oley, C.A.4
Flint, J.5
Wolstenholme, J.6
Duckett, D.P.7
Barrow, M.A.8
Leonard, J.V.9
Read, A.P.10
Trembath, R.C.11
|