138 related articles for article (PubMed ID: 4020801)
1. Congenital adrenal hyperplasia and XYY hypogonadism.
Abraham RR; Wynn V; Heaton DE
J R Soc Med; 1985 Aug; 78(8):672-4. PubMed ID: 4020801
[No Abstract] [Full Text] [Related]
2. Effects of the XYY karyotype in one of two brothers with congenital adrenal hyperplasia.
Mallin SR; Walker FA
Clin Genet; 1972; 3(6):490-4. PubMed ID: 4510131
[No Abstract] [Full Text] [Related]
3. Deletion of the long arm of the Y chromosome in an adolescent with short stature and hypogonadism.
Botella-Carretero JI; Valero MA; Valcorba I; Ezquieta B; Alonso M; Barrio R
J Pediatr Endocrinol Metab; 2001 Jan; 14(1):103-6. PubMed ID: 11220698
[TBL] [Abstract][Full Text] [Related]
4. XYY karyotype with severe primary hypogonadism. A case report.
Puavilai G; Himathongkam T; Mekanandha V; Chuahirun S; Kitivat N
J Med Assoc Thai; 1982 May; 65(5):277-82. PubMed ID: 7119627
[No Abstract] [Full Text] [Related]
5. Hypogonadotropic hypogonadism; the genetic defect. A hypothesis based on human and animal prototypes.
Dacou-Voutetakis C
Horm Res; 1992; 37 Suppl 3():62-4. PubMed ID: 1427644
[TBL] [Abstract][Full Text] [Related]
6. Genetic analysis of NR0B1 in congenital adrenal hypoplasia patients: identification of a rare regulatory variant resulting in congenital adrenal hypoplasia and hypogonadal hypogonadism without testicular carcinoma in situ.
Walker AP; Fowkes RC; Saleh F; Kim SH; Wilkinson P; Cabrera-Sharp V; Talmud PJ; Humphries SE; Looijenga LH; Bouloux PM
Sex Dev; 2012; 6(6):284-91. PubMed ID: 23018754
[TBL] [Abstract][Full Text] [Related]
7. XYY syndrome and acute myeloblastic leukemia.
Midro AT; Wojtukiewicz M; Bielawiec M; Sawicka A
Cancer Genet Cytogenet; 1987 Feb; 24(2):363-5. PubMed ID: 3466685
[TBL] [Abstract][Full Text] [Related]
8. A microdeletion within DAX-1 in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.
Wang J; Killinger DW; Hegele RA
J Investig Med; 1999 May; 47(5):232-5. PubMed ID: 10361383
[TBL] [Abstract][Full Text] [Related]
9. Sexual infantilism related to adrenogenital syndrome in conjunction with a chromosomal defect.
Check JH; Goldfarb AF; Rakoff AE; Jackson L
Am J Obstet Gynecol; 1977 Dec; 129(8):919-20. PubMed ID: 930977
[No Abstract] [Full Text] [Related]
10. Triple-x syndrome accompanied by congenital adrenal hyperplasia: case report.
Kurtoğlu S; Atabek ME; Akçakuş M; Ozkul Y; Saatçi C
Turk J Pediatr; 2004; 46(4):377-9. PubMed ID: 15641277
[TBL] [Abstract][Full Text] [Related]
11. A de novo mutation of DAX1 in a boy with congenital adrenal hypoplasia without hypogonadotropic hypogonadism.
Wang CL; Fen ZW; Liang L
J Pediatr Endocrinol Metab; 2014 Mar; 27(3-4):343-7. PubMed ID: 24197767
[TBL] [Abstract][Full Text] [Related]
12. Two transsexuals with 47-XYY karyotype.
Buhrich N; Barr R; Lam-Po-Tang PR
Br J Psychiatry; 1978 Jul; 133():77-81. PubMed ID: 667511
[TBL] [Abstract][Full Text] [Related]
13. XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning.
Fryns JP; Kleczkowska A; Kubień E; Van den Berghe H
Genet Couns; 1995; 6(3):197-206. PubMed ID: 8588846
[TBL] [Abstract][Full Text] [Related]
14. Congenital adrenal hypoplasia and hypogonadotropic hypogonadism: phenotypic variability of the DAX-1 gene R267P mutation.
Sánchez-Pacheco M; Moreno-Pérez O; Sánchez-Ortiga R; Picó A; Moreno F
Endocrinol Nutr; 2012 Feb; 59(2):140-2. PubMed ID: 21925982
[No Abstract] [Full Text] [Related]
15. [A case of Addison's disease associated with hypogonadotropic hypogonadism].
Oe K; Koto K; Onaka K; Yanase T; Tsuji Y; Katsuno M; Takayanagi R; Tsuchimoro M; Nanita A
Nihon Naika Gakkai Zasshi; 1993 Jun; 82(6):911-3. PubMed ID: 8360574
[No Abstract] [Full Text] [Related]
16. Abnormal sex chromosome constitution and longitudinal growth: serum levels of insulin-like growth factor (IGF)-I, IGF binding protein-3, luteinizing hormone, and testosterone in 109 males with 47,XXY, 47,XYY, or sex-determining region of the Y chromosome (SRY)-positive 46,XX karyotypes.
Aksglaede L; Skakkebaek NE; Juul A
J Clin Endocrinol Metab; 2008 Jan; 93(1):169-76. PubMed ID: 17940117
[TBL] [Abstract][Full Text] [Related]
17. Oligohydramnios syndrome and XYY karyotype.
Côté GB; Tsomi K; Papadakou-Lagoyanni S; Petmezaki S
Ann Genet; 1978 Dec; 21(4):226-8. PubMed ID: 314260
[TBL] [Abstract][Full Text] [Related]
18. [The diagnostic procedure in primary amenorrhea].
Kumschick H; Hauser GA
Schweiz Med Wochenschr; 1966 Aug; 96(33):1055-65. PubMed ID: 5997652
[No Abstract] [Full Text] [Related]
19. 48,XYY,+13 karyotype in a liveborn infant.
Crolla JA; Machin GA
Clin Genet; 1980 Jan; 17(1):31-4. PubMed ID: 7389183
[TBL] [Abstract][Full Text] [Related]
20. Intersexuality: definitions, diagnosis, and dilemmas.
Grace HJ
Arch Androl; 1986; 17(2):129-31. PubMed ID: 3827385
[No Abstract] [Full Text] [Related]
[Next] [New Search]
