-
1
-
-
0029069878
-
Androgen receptor defects: Historical, clinical, and molecular perspectives
-
Quigley CA, De Bellis A, Marschke KB, El-Awady MK, Wilson EM, French FS. Androgen receptor defects: historical, clinical, and molecular perspectives. Endocr Rev 1995; 16: 271-321.
-
(1995)
Endocr Rev
, vol.16
, pp. 271-321
-
-
Quigley, C.A.1
De Bellis, A.2
Marschke, K.B.3
El-Awady, M.K.4
Wilson, E.M.5
French, F.S.6
-
2
-
-
0025582865
-
Molecular basis of androgen insensitivity
-
French FS, Lubahn DB, Brown TR, Simental JA, Quigley CA, Yarbrough WG, Tan JA, Sar M, Joseph DR, Evans BA, et al. Molecular basis of androgen insensitivity. Rec Prog Horm Res 1990; 46: 1-38.
-
(1990)
Rec Prog Horm Res
, vol.46
, pp. 1-38
-
-
French, F.S.1
Lubahn, D.B.2
Brown, T.R.3
Simental, J.A.4
Quigley, C.A.5
Yarbrough, W.G.6
Tan, J.A.7
Sar, M.8
Joseph, D.R.9
Evans, B.A.10
-
3
-
-
0035919213
-
Molecular basis of androgen insensitivity
-
Brinkmann AO. Molecular basis of androgen insensitivity. Mol Cell Endocrinol 2001; 179: 105-109.
-
(2001)
Mol Cell Endocrinol
, vol.179
, pp. 105-109
-
-
Brinkmann, A.O.1
-
4
-
-
0033343118
-
A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred
-
Zhu YS, Cai LQ, Cordero JJ, Canovatchel WJ, Katz MD, Imperato-McGinley J. A novel mutation in the CAG triplet region of exon 1 of androgen receptor gene causes complete androgen insensitivity syndrome in a large kindred. J Clin Endocrinol Metab 1999; 84: 1590-1594.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 1590-1594
-
-
Zhu, Y.S.1
Cai, L.Q.2
Cordero, J.J.3
Canovatchel, W.J.4
Katz, M.D.5
Imperato-McGinley, J.6
-
5
-
-
0028214313
-
Detection of point mutations in the androgen receptor gene using non-isotopic single strand conformation polymorphism analysis
-
Hiort O, Wodtke A, Struve D, Zöllner A, Sinnecker GH. Detection of point mutations in the androgen receptor gene using non-isotopic single strand conformation polymorphism analysis. Hum Mol Genet 1994; 3: 1163-1166.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1163-1166
-
-
Hiort, O.1
Wodtke, A.2
Struve, D.3
Zöllner, A.4
Sinnecker, G.H.5
-
7
-
-
0026939531
-
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome
-
Batch JA, Williams DM, Davies HR, Brown BD, Evans BA, Hughes IA, Patterson MN. Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome. Hum Mol Genet 1992; 1: 497-503.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 497-503
-
-
Batch, J.A.1
Williams, D.M.2
Davies, H.R.3
Brown, B.D.4
Evans, B.A.5
Hughes, I.A.6
Patterson, M.N.7
-
8
-
-
0027315881
-
Molecular genetics of human androgen insensitivity
-
Brown TR, Scherer PA, Chang YT, Migeon CJ, Ghirri P, Murono K, Zhou Z. Molecular genetics of human androgen insensitivity. Eur J Pediatr 1993; 152 (Suppl 2): S62-69.
-
(1993)
Eur J Pediatr
, vol.152
, Issue.SUPPL. 2
-
-
Brown, T.R.1
Scherer, P.A.2
Chang, Y.T.3
Migeon, C.J.4
Ghirri, P.5
Murono, K.6
Zhou, Z.7
-
9
-
-
0029986454
-
The clinical and molecular spectrum of androgen insensitivity syndromes
-
Hiort O, Sinnecker GH, Holterhus PM, Nitsche EM, Kruse K. The clinical and molecular spectrum of androgen insensitivity syndromes. Am J Med Genet 1996; 63: 218-222.
-
(1996)
Am J Med Genet
, vol.63
, pp. 218-222
-
-
Hiort, O.1
Sinnecker, G.H.2
Holterhus, P.M.3
Nitsche, E.M.4
Kruse, K.5
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