141 related articles for article (PubMed ID: 4556550)
1. Genetic disorders affecting genital development in 46,XY individuals (male pseudohermaphroditism).
Sarto GE
Clin Obstet Gynecol; 1972 Mar; 15(1):183-202. PubMed ID: 4556550
[No Abstract] [Full Text] [Related]
2. Differential diagnosis of genital ambiguity in the newborn.
Summitt RL
Clin Obstet Gynecol; 1972 Mar; 15(1):112-40. PubMed ID: 4556547
[No Abstract] [Full Text] [Related]
3. Hypogonadism in chromatin-negative phenotypic male subjects.
Donohue JP
J Urol; 1970 May; 103(5):645-51. PubMed ID: 5309808
[No Abstract] [Full Text] [Related]
4. [Case of familial hypoplasia of male genitalia (Reifenstein's syndrome?)].
Uetani K; Kaneta T
Horumon To Rinsho; 1973 Dec; 21(12):1255-8. PubMed ID: 4798491
[No Abstract] [Full Text] [Related]
5. Androgen-insensitive male pseudohermaphroditism.
Jirásek JE
Birth Defects Orig Artic Ser; 1971 May; 7(6):179-84. PubMed ID: 5173159
[TBL] [Abstract][Full Text] [Related]
6. Reifenstein's syndrome: hereditary familial hypogonadism with hypospadias and gynecomastia.
Jones LW; Isaacs H; Edelbrock H; Donnell GN
J Urol; 1970 Oct; 104(4):608-11. PubMed ID: 5476478
[No Abstract] [Full Text] [Related]
7. Diagnosis and management of the infant with genital ambiguity.
Simpson JL
Am J Obstet Gynecol; 1977 May; 128(2):137-45. PubMed ID: 855867
[TBL] [Abstract][Full Text] [Related]
8. HEREDITARY MALE PSEUDOHERMAPHRODITISM WITH HYPOGONADISM, HYPOSPADIAS, AND GYNECOMASTIA: REIFENSTEIN'S SYNDROME.
BOWEN P; LEE CS; MIGEON CJ; KAPLAN NM; WHALLEY PJ; MCKUSICK VA; REINFENSTEIN EC
Ann Intern Med; 1965 Feb; 62():252-70. PubMed ID: 14259209
[No Abstract] [Full Text] [Related]
9. Male pseudohermaphroditism: the complexities of male phenotypic development.
Imperato-McGinley J; Peterson RE
Am J Med; 1976 Aug; 61(2):251-72. PubMed ID: 181986
[No Abstract] [Full Text] [Related]
10. Human male sexual maldevelopment: teratogenetic classification of monogenic forms.
Pinsky L
Teratology; 1974 Oct; 10(2):193-203. PubMed ID: 4610880
[No Abstract] [Full Text] [Related]
11. Pseudovaginal perineoscrotal hypospadias.
Opitz JM; Simpson JL; Sarto GE; Summitt RL; New M; German J
Clin Genet; 1972; 3(1):1-26. PubMed ID: 5013863
[No Abstract] [Full Text] [Related]
12. Reifenstein's syndrome, a 17beta-hydroxysteroid-oxydoreductase deficiency?
Knorr D; Bidlingmaier F; Engelhardt D
Acta Endocrinol Suppl (Copenh); 1973; 173():37. PubMed ID: 4542115
[No Abstract] [Full Text] [Related]
13. Xg groups and sex abnormalities in people of northern European ancestry.
Sanger R; Tippett P; Gavin J
J Med Genet; 1971 Dec; 8(4):417-26. PubMed ID: 5149524
[No Abstract] [Full Text] [Related]
14. Male hypogonadism: Klinefelter and Reifenstein syndromes.
Leonard JM; Bremner WJ; Capell PT; Paulsen CA
Birth Defects Orig Artic Ser; 1975; 11(4):17-22. PubMed ID: 1156685
[No Abstract] [Full Text] [Related]
15. Etiological diagnosis of undervirilized male/XY disorder of sex development.
Atta I; Ibrahim M; Parkash A; Lone SW; Khan YN; Raza J
J Coll Physicians Surg Pak; 2014 Oct; 24(10):714-8. PubMed ID: 25327912
[TBL] [Abstract][Full Text] [Related]
16. Familial incomplete male pseudohermaphroditism, type 1. Evidence for androgen resistance and variable clinical manifestations in a family with the Reifenstein syndrome.
Wilson JD; Harrod MJ; Goldstein JL; Hemsell DL; MacDonald PC
N Engl J Med; 1974 May; 290(20):1097-103. PubMed ID: 4821173
[No Abstract] [Full Text] [Related]
17. Testicular feminization syndrome: current clinical considerations.
Glenn JF
Urology; 1976 Jun; 7(6):569-77. PubMed ID: 779212
[TBL] [Abstract][Full Text] [Related]
18. Clinical, hormonal, behavioral, and genetic characteristics of androgen insensitivity syndrome in a Brazilian cohort: five novel mutations in the androgen receptor gene.
Melo KF; Mendonca BB; Billerbeck AE; Costa EM; Inácio M; Silva FA; Leal AM; Latronico AC; Arnhold IJ
J Clin Endocrinol Metab; 2003 Jul; 88(7):3241-50. PubMed ID: 12843171
[TBL] [Abstract][Full Text] [Related]
19. Gynecomastia as a familial incomplete male pseudohermaphroditism type 1: a limited androgen resistance syndrome.
Larrea F; Benavides G; Scaglia H; Kofman-Alfaro S; Ferrusca E; Medina M; Pérez-Palacios G
J Clin Endocrinol Metab; 1978 Jun; 46(6):961-70. PubMed ID: 122442
[TBL] [Abstract][Full Text] [Related]
20. Familial Leydig cell hypoplasia as a cause of male pseudohermaphroditism.
el-Awady MK; Temtamy SA; Salam MA; Gad YZ
Hum Hered; 1987; 37(1):36-40. PubMed ID: 3557461
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
