-
1
-
-
0033118412
-
Mammalian sex determination: A molecular drama
-
Swain A & Lovell-Badge R. Mammalian sex determination: A molecular drama. Genes and Development 1999; 13: 735-767.
-
(1999)
Genes and Development
, vol.13
, pp. 735-767
-
-
Swain, A.1
Lovell-Badge, R.2
-
4
-
-
0003070938
-
Sexual differentiation and ambiguity
-
In Kappy MS, Blizzard RM & Migeon CJ (eds); Springfield, III: Charles C Thomas Publisher
-
Migeon CJM, Berkowitz G & Brown TR. Sexual differentiation and ambiguity. In Kappy MS, Blizzard RM & Migeon CJ (eds) The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence, 4th edn. Springfield, III: Charles C Thomas Publisher, 1994, pp 573-715.
-
(1994)
The Diagnosis and Treatment of Endocrine Disorders in Childhood and Adolescence, 4th edn
, pp. 573-715
-
-
Migeon, C.J.M.1
Berkowitz, G.2
Brown, T.R.3
-
5
-
-
0034798865
-
Müllerian inhibiting substance: An instructive developmental hormone with diagnostic and possible therapeutic applications
-
Teixeira J, Maheswaran S & Donahoe PK. Müllerian inhibiting substance: An instructive developmental hormone with diagnostic and possible therapeutic applications. Endocrine Reviews 2001; 22: 657-674.
-
(2001)
Endocrine Reviews
, vol.22
, pp. 657-674
-
-
Teixeira, J.1
Maheswaran, S.2
Donahoe, P.K.3
-
7
-
-
0009035309
-
Male pseudohermaphroditism: A hitherto undescribed form
-
Swyer GIM. Male pseudohermaphroditism: A hitherto undescribed form. British Medical Journal 1955; 2: 709-712.
-
(1955)
British Medical Journal
, vol.2
, pp. 709-712
-
-
Swyer, G.I.M.1
-
8
-
-
0015953713
-
Testosterone formation and metabolism during male sexual differentiation in the human embryo
-
Siitera PK & Wilson JD. Testosterone formation and metabolism during male sexual differentiation in the human embryo. Journal of Clinical Endocrinology and Metabolism 1974; 38: 113.
-
(1974)
Journal of Clinical Endocrinology and Metabolism
, vol.38
, pp. 113
-
-
Siitera, P.K.1
Wilson, J.D.2
-
12
-
-
0035032083
-
Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency: Growth, development and therapeutic considerations
-
Migeon CJ & Wisniewski AB. Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency: Growth, development and therapeutic considerations. Endocrinology and Metabolism Clinics of North America 2001; 30: 193-206.
-
(2001)
Endocrinology and Metabolism Clinics of North America
, vol.30
, pp. 193-206
-
-
Migeon, C.J.1
Wisniewski, A.B.2
-
13
-
-
0019431889
-
Acquired adrenal hyperplasia: With special reference to 3 beta-hydroxysteroid dehydrogenase
-
Bongiovanni AM. Acquired adrenal hyperplasia: With special reference to 3 beta-hydroxysteroid dehydrogenase. Fertility and Sterility 1981; 35: 599-608.
-
(1981)
Fertility and Sterility
, vol.35
, pp. 599-608
-
-
Bongiovanni, A.M.1
-
15
-
-
84882737894
-
Nebenniereninsuffizienz bei kongenitaler Lipoidhyperplasie der Nebennieren
-
Prader A & Siebenmann RE. Nebenniereninsuffizienz bei kongenitaler Lipoidhyperplasie der Nebennieren. Helv Paediat Acta 1957; 12: 69.
-
(1957)
Helv Paediat Acta
, vol.12
, pp. 69
-
-
Prader, A.1
Siebenmann, R.E.2
-
16
-
-
0031550935
-
Paternity by intrauterine insemination with sperm from a man with 5alpha-reductase-2 deficiency
-
Katz MD, Kligman I, Cai LQ et al. Paternity by intrauterine insemination with sperm from a man with 5alpha-reductase-2 deficiency. New England Journal of Medicine 1997; 336: 994-997.
-
(1997)
New England Journal of Medicine
, vol.336
, pp. 994-997
-
-
Katz, M.D.1
Kligman, I.2
Cai, L.Q.3
-
17
-
-
0033233294
-
17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations
-
Boehmer ALM, Brinkmann AO, Sandkuijl LA et al. 17β-Hydroxysteroid dehydrogenase-3 deficiency: Diagnosis, phenotypic variability, population genetics, and worldwide distribution of ancient and de novo mutations. Journal of Clinical Endocrinology and Metabolism 1999; 84: 4713-4721.
-
(1999)
Journal of Clinical Endocrinology and Metabolism
, vol.84
, pp. 4713-4721
-
-
Boehmer, A.L.M.1
Brinkmann, A.O.2
Sandkuijl, L.A.3
-
19
-
-
0037158472
-
Parental origin of normal X chromosomes in Turner syndrome patients with various karyotype: Implications for the mechanism leading to generation of a 45,X karyotype
-
Uematsu A, Yorifuji T, Muroi J et al. Parental origin of normal X chromosomes in Turner syndrome patients with various karyotype: Implications for the mechanism leading to generation of a 45,X karyotype. American Journal of Medical Genetics 2002; 111: 134-139.
-
(2002)
American Journal of Medical Genetics
, vol.111
, pp. 134-139
-
-
Uematsu, A.1
Yorifuji, T.2
Muroi, J.3
-
20
-
-
0036278097
-
Growth failure in early life: An important manifestation of Turner syndrome
-
Davenport ML, Punyasavatsut N, Stewart PW et al. Growth failure in early life: An important manifestation of Turner syndrome. Hormone Research 2002; 57: 157-164.
-
(2002)
Hormone Research
, vol.57
, pp. 157-164
-
-
Davenport, M.L.1
Punyasavatsut, N.2
Stewart, P.W.3
-
23
-
-
0036717190
-
Ambiguous genitalia with perineo-scrotal hypospadias in 46,XY individuals: Long-term medical, surgical and psychosexual outcome
-
Migeon CJ, Wisniewski AB, Gearhart JP et al. Ambiguous genitalia with perineo-scrotal hypospadias in 46,XY individuals: Long-term medical, surgical and psychosexual outcome. Journal of Paediatrics 2002; 110: e31.
-
(2002)
Journal of Paediatrics
, vol.110
-
-
Migeon, C.J.1
Wisniewski, A.B.2
Gearhart, J.P.3
-
24
-
-
0036719367
-
46,XY intersex subjects: Phenotypic and etiologic classification, knowledge of condition and satisfaction with knowledge in adulthood
-
Migeon CJ, Wisniewski AB, Brown TR, et al. 46,XY intersex subjects: Phenotypic and etiologic classification, knowledge of condition and satisfaction with knowledge in adulthood. Journal of Paediatrics 2002; 110: e32.
-
(2002)
Journal of Paediatrics
, vol.110
-
-
Migeon, C.J.1
Wisniewski, A.B.2
Brown, T.R.3
|