-
1
-
-
0344819243
-
Molecular genetics and pathophysiology of 17b-hydroxysteroid dehydrogenase 3 deficiency
-
Andersson S, Geissler WM, Wu L, Davis D, Grumbach MM, New MI, Schwarz HP, Blethen SL, Mendonca BB, Bloise W, Witchel SF, Cutler GB Jr, Griffin JE, Wilson JD, Russell DW (1996): Molecular genetics and pathophysiology of 17b-hydroxysteroid dehydrogenase 3 deficiency. J Clin Endocrinol Metab 81:130-136.
-
(1996)
J Clin Endocrinol Metab
, vol.81
, pp. 130-136
-
-
Andersson, S.1
Geissler, W.M.2
Wu, L.3
Davis, D.4
Grumbach, M.M.5
New, M.I.6
Schwarz, H.P.7
Blethen, S.L.8
Mendonca, B.B.9
Bloise, W.10
Witchel, S.F.11
Cutler Jr., G.B.12
Griffin, J.E.13
Wilson, J.D.14
Russell, D.W.15
-
2
-
-
0015597377
-
A familial syndrome deafness, alopecia, and hypogonadism
-
Crandall BF, Samec L, Sparkes RS, Wright SW (1973): A familial syndrome deafness, alopecia, and hypogonadism. J Pediatr 82:461-465.
-
(1973)
J Pediatr
, vol.82
, pp. 461-465
-
-
Crandall, B.F.1
Samec, L.2
Sparkes, R.S.3
Wright, S.W.4
-
3
-
-
0024578576
-
The nature of the defect in male pseudohermaphroiditism in Arabs of Gaza
-
Eckstein B, Cohen S, Farkass A, Rösler A (1989): The nature of the defect in male pseudohermaphroiditism in Arabs of Gaza. J Clin Endocrinol Metab 68:477-485.
-
(1989)
J Clin Endocrinol Metab
, vol.68
, pp. 477-485
-
-
Eckstein, B.1
Cohen, S.2
Farkass, A.3
Rösler, A.4
-
4
-
-
0027930787
-
Male pseudohermaphroditism caused by mutations of testicular 17b-hydroxysteroid dehydrogenase 3
-
Geissler WM, Davis DL, Wu L, Bradshaw KD, Patel S, Mendonca BB, Elliston KO, Wilson JD, Russel DW, Andersson S (1994): Male pseudohermaphroditism caused by mutations of testicular 17b-hydroxysteroid dehydrogenase 3. Nature Genet 7:34-39.
-
(1994)
Nature Genet
, vol.7
, pp. 34-39
-
-
Geissler, W.M.1
Davis, D.L.2
Wu, L.3
Bradshaw, K.D.4
Patel, S.5
Mendonca, B.B.6
Elliston, K.O.7
Wilson, J.D.8
Russel, D.W.9
Andersson, S.10
-
5
-
-
0022447457
-
Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Gender reassignment in early infancy
-
Gross D, Kohn G, Farkas A, Landau H, Elrayyes E, El-Shawwa R, Lasch EE, Rösler A (1986): Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Gender reassignment in early infancy. Acta Endocrinol 112:238-246.
-
(1986)
Acta Endocrinol
, vol.112
, pp. 238-246
-
-
Gross, D.1
Kohn, G.2
Farkas, A.3
Landau, H.4
Elrayyes, E.5
El-Shawwa, R.6
Lasch, E.E.7
Rösler, A.8
-
6
-
-
0026059417
-
Normative data for adrenal steroidogenesis in a healthy pediatric population: Age- and sex-related changes after adrenocorticotropin stimulation
-
Lashansky G, Saenger P, Fishman K, Gautier T, Mayes D, Berg G, DiMaritino-Nardi J, Reiter E (1991): Normative data for adrenal steroidogenesis in a healthy pediatric population: Age- and sex-related changes after adrenocorticotropin stimulation. J Clin Endocrinol Metab 73:674-686.
-
(1991)
J Clin Endocrinol Metab
, vol.73
, pp. 674-686
-
-
Lashansky, G.1
Saenger, P.2
Fishman, K.3
Gautier, T.4
Mayes, D.5
Berg, G.6
Dimaritino-Nardi, J.7
Reiter, E.8
-
7
-
-
0027097126
-
Steroid 17b-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism
-
Rösler A (1992): Steroid 17b-hydroxysteroid dehydrogenase deficiency in man: An inherited form of male pseudohermaphroditism. J Steroid Biochem Molec Biol 43:989-1002.
-
(1992)
J Steroid Biochem Molec Biol
, vol.43
, pp. 989-1002
-
-
Rösler, A.1
-
8
-
-
0020791429
-
Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role
-
Rösler A, Kohn G (1983): Male pseudohermaphroditism due to 17b-hydroxysteroid dehydrogenase deficiency: Studies on the natural history of the defect and effect of androgens on gender role. J Steroid Biochem 19:663-674.
-
(1983)
J Steroid Biochem
, vol.19
, pp. 663-674
-
-
Rösler, A.1
Kohn, G.2
-
9
-
-
0029940067
-
A (R80Q) mutation in 17b-hydroxysteroid dehydrogenase type 3 gene among Arabs of Israel is associated with pseudohermaphroditism in males and normal asymptomatic females
-
Rösler A, Silverstein S, Abeliovich D (1996): A (R80Q) mutation in 17b-hydroxysteroid dehydrogenase type 3 gene among Arabs of Israel is associated with pseudohermaphroditism in males and normal asymptomatic females. J Clin Endoctrinol Metab 81:1827-1831.
-
(1996)
J Clin Endoctrinol Metab
, vol.81
, pp. 1827-1831
-
-
Rösler, A.1
Silverstein, S.2
Abeliovich, D.3
-
10
-
-
0020579362
-
A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities
-
Woodhouse NJY, Sakati NA (1983): A syndrome of hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and ECG abnormalities. J Med Genet 20:216-219.
-
(1983)
J Med Genet
, vol.20
, pp. 216-219
-
-
Woodhouse, N.J.Y.1
Sakati, N.A.2
|