-
3
-
-
85028288395
-
Size at birth and early childhood growth in relation to maternal smoking, parity and infant breast-feeding: Longitudinal birth cohort study and analysis
-
Ong KK, Preece MA, Emmett PM, et al. Size at birth and early childhood growth in relation to maternal smoking, parity and infant breast-feeding: longitudinal birth cohort study and analysis. Pediatr Res 2002;52:863-7.
-
(2002)
Pediatr Res
, vol.52
, pp. 863-867
-
-
Ong, K.K.1
Preece, M.A.2
Emmett, P.M.3
-
4
-
-
34447130903
-
Human sexual size dimorphism in early pregnancy
-
Bukowski R, Smith GC, Malone FD, et al. Human sexual size dimorphism in early pregnancy. Am J Epidemiol 2007;165:1216-18.
-
(2007)
Am J Epidemiol
, vol.165
, pp. 1216-1218
-
-
Bukowski, R.1
Smith, G.C.2
Malone, F.D.3
-
7
-
-
0034454269
-
Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
-
White PC, Speiser PW. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Endocr Rev 2000;21:245-91.
-
(2000)
Endocr Rev
, vol.21
, pp. 245-291
-
-
White, P.C.1
Speiser, P.W.2
-
8
-
-
0033311160
-
Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency
-
Nordenström A, Thilén A, Hagenfeldt L, et al. Genotyping is a valuable diagnostic complement to neonatal screening for congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency. J Clin Endocrinol Metab 1999;84:1505-9.
-
(1999)
J Clin Endocrinol Metab
, vol.84
, pp. 1505-1509
-
-
Nordenström, A.1
Thilén, A.2
Hagenfeldt, L.3
-
9
-
-
0026939531
-
Androgen receptor gene mutations identified by SSCP in fourteen subjects with androgen insensitivity syndrome
-
Batch JA, Williams DM, Davies HR, et al. 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
-
10
-
-
0030059911
-
Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome
-
Bevan CL, Brown BB, Davies HR, et al. Functional analysis of six androgen receptor mutations identified in patients with partial androgen insensitivity syndrome. Hum Mol Genet 1996;5:265-73.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 265-273
-
-
Bevan, C.L.1
Brown, B.B.2
Davies, H.R.3
-
11
-
-
0029000469
-
Cross sectional stature and weight reference curves for the UK, 1990
-
Freeman JV, Cole TJ, Chinn S, et al. Cross sectional stature and weight reference curves for the UK, 1990. Arch Dis Child 1995;73:17-24.
-
(1995)
Arch Dis Child
, vol.73
, pp. 17-24
-
-
Freeman, J.V.1
Cole, T.J.2
Chinn, S.3
-
12
-
-
0027159735
-
Steroid 21-hydroxylase deficiency: Two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations
-
Wedell A, Luthman H. Steroid 21-hydroxylase deficiency: two additional mutations in salt-wasting disease and rapid screening of disease-causing mutations. Hum Mol Genet 1993;2:499-504.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 499-504
-
-
Wedell, A.1
Luthman, H.2
-
13
-
-
0021843905
-
Testosterone levels in midtrimester maternal and fetal plasma and amniotic fluid
-
Rodeck CH, Gill D, Rosenberg DA, et al. Testosterone levels in midtrimester maternal and fetal plasma and amniotic fluid. Prenat Diagn 1985;5:175-81.
-
(1985)
Prenat Diagn
, vol.5
, pp. 175-181
-
-
Rodeck, C.H.1
Gill, D.2
Rosenberg, D.A.3
-
15
-
-
35448970588
-
Amniotic fluid testosterone: Relationship with cortisol and gestational age
-
Sarkar P, Bergman K, Fisk NM, et al. Amniotic fluid testosterone: relationship with cortisol and gestational age. Clin Endocrinol (Oxf) 2007;67:743-7.
-
(2007)
Clin Endocrinol (Oxf)
, vol.67
, pp. 743-747
-
-
Sarkar, P.1
Bergman, K.2
Fisk, N.M.3
-
16
-
-
0021689502
-
Specific 5 alpha-dihydrotestosterone receptor and 5 alpha-reductase activity in human amniotic fluid cells
-
Sultan C, Emberger JM, Devillier C, et al. Specific 5 alpha-dihydrotestosterone receptor and 5 alpha-reductase activity in human amniotic fluid cells. Am J Obstet Gynecol 1984;150:956-60.
-
(1984)
Am J Obstet Gynecol
, vol.150
, pp. 956-960
-
-
Sultan, C.1
Emberger, J.M.2
Devillier, C.3
-
17
-
-
4544329837
-
Immunohistochemical localization of androgen receptors in the urogenital tracts of human embryos
-
Sajjad Y, Quenby S, Nickson P, et al. Immunohistochemical localization of androgen receptors in the urogenital tracts of human embryos. Reproduction 2004;128:331-9.
-
(2004)
Reproduction
, vol.128
, pp. 331-339
-
-
Sajjad, Y.1
Quenby, S.2
Nickson, P.3
-
18
-
-
0030879496
-
Development and characterization of a conditionally immortalized human osteoblastic cell line stably transfected with the human androgen receptor gene
-
Hofbauer LC, Hicok KC, Schroeder MJ, et al. Development and characterization of a conditionally immortalized human osteoblastic cell line stably transfected with the human androgen receptor gene. J Cell Biochem 1997;66:542-51.
-
(1997)
J Cell Biochem
, vol.66
, pp. 542-551
-
-
Hofbauer, L.C.1
Hicok, K.C.2
Schroeder, M.J.3
-
19
-
-
33646466295
-
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes
-
Balsamo A, Wasniewska M, Di Pasquale G, et al. Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. Eur J Pediatr 2006;165:380-3.
-
(2006)
Eur J Pediatr
, vol.165
, pp. 380-383
-
-
Balsamo, A.1
Wasniewska, M.2
Di Pasquale, G.3
-
20
-
-
33846111438
-
Gestational age correlates to genotype in girls with CYP21 deficiency
-
Gidlöf S, Wedell A, Nordenström A. Gestational age correlates to genotype in girls with CYP21 deficiency. J Clin Endocrinol Metab 2007;92:246-9.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 246-249
-
-
Gidlöf, S.1
Wedell, A.2
Nordenström, A.3
-
21
-
-
0032004161
-
Sexual dimorphism in primate neonatal body mass
-
Smith RJ, Leigh SR. Sexual dimorphism in primate neonatal body mass. J Hum Evol 1998;34:173-201.
-
(1998)
J Hum Evol
, vol.34
, pp. 173-201
-
-
Smith, R.J.1
Leigh, S.R.2
-
22
-
-
0015189703
-
The effects of chromosome abnormalities on birth weight in man. I. Sex chromosome disorders
-
Chen AT, Chan YK, Falek A. The effects of chromosome abnormalities on birth weight in man. I. Sex chromosome disorders. Hum Hered 1971;21:543-56.
-
(1971)
Hum Hered
, vol.21
, pp. 543-556
-
-
Chen, A.T.1
Chan, Y.K.2
Falek, A.3
-
23
-
-
0028528510
-
Root length, crown height, and root morphology in Turner syndrome
-
Midtbø M, Halse A. Root length, crown height, and root morphology in Turner syndrome. Acta Odontol Scand 1994;52:303-14.
-
(1994)
Acta Odontol Scand
, vol.52
, pp. 303-314
-
-
Midtbø, M.1
Halse, A.2
-
24
-
-
25844463681
-
Root growth in the teeth of 46,XY females
-
Lähdesmäki R, Alvesalo L. Root growth in the teeth of 46,XY females. Arch Oral Biol 2005;50:947-52.
-
(2005)
Arch Oral Biol
, vol.50
, pp. 947-952
-
-
Lähdesmäki, R.1
Alvesalo, L.2
-
25
-
-
34547187279
-
Root lengths in the permanent teeth of Klinefelter (47,XXY) men
-
Lähdesmäki R, Alvesalo L. Root lengths in the permanent teeth of Klinefelter (47,XXY) men. Arch Oral Biol 2007;52:822-7.
-
(2007)
Arch Oral Biol
, vol.52
, pp. 822-827
-
-
Lähdesmäki, R.1
Alvesalo, L.2
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