Page last updated: 2024-08-17

androstenedione and Abnormalities, Congenital

androstenedione has been researched along with Abnormalities, Congenital in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (50.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Biason-Lauber, A; Gueorguieva, I; Lebon-Labich, B; Paris, F; Philibert, P; Pienkowski, C; Stuckens, C; Sultan, C	1
Chrz, R; Kobilková, J; Málková, J; Motlík, K; Silinková-Málková, E; Stárka, L	1

Other Studies

2 other study(ies) available for androstenedione and Abnormalities, Congenital

Article	Year
Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome). Fertility and sterility, 2011, Jun-30, Volume: 95, Issue:8 Topics: 17-alpha-Hydroxyprogesterone; 46, XX Disorders of Sex Development; Abnormalities, Multiple; Adolescent; Androstenedione; beta Catenin; Cell Line, Tumor; Congenital Abnormalities; Dehydroepiandrosterone; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Hyperandrogenism; Kidney; Mullerian Ducts; Mutation; Ovary; Phenotype; Progesterone Reductase; RNA, Messenger; Somites; Spine; Steroid 17-alpha-Hydroxylase; Transfection; Uterus; Vagina; Wnt Proteins; Wnt4 Protein; Young Adult	2011
46, XX gonadal dysgenesis and ovarian hypoplasia. Humangenetik, 1974, Volume: 23, Issue:3 Topics: Adolescent; Adult; Androstenedione; Congenital Abnormalities; Female; Humans; Hydroxyprogesterones; Maternal Age; Ovarian Diseases; Ovary; Pedigree; Testosterone; Turner Syndrome	1974

Article

Year

Molecular analysis of WNT4 gene in four adolescent girls with mullerian duct abnormality and hyperandrogenism (atypical Mayer-Rokitansky-Küster-Hauser syndrome).

Fertility and sterility, 2011, Jun-30, Volume: 95, Issue:8

Topics: 17-alpha-Hydroxyprogesterone; 46, XX Disorders of Sex Development; Abnormalities, Multiple; Adolescent; Androstenedione; beta Catenin; Cell Line, Tumor; Congenital Abnormalities; Dehydroepiandrosterone; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heterozygote; Humans; Hyperandrogenism; Kidney; Mullerian Ducts; Mutation; Ovary; Phenotype; Progesterone Reductase; RNA, Messenger; Somites; Spine; Steroid 17-alpha-Hydroxylase; Transfection; Uterus; Vagina; Wnt Proteins; Wnt4 Protein; Young Adult

2011

46, XX gonadal dysgenesis and ovarian hypoplasia.

Humangenetik, 1974, Volume: 23, Issue:3

Topics: Adolescent; Adult; Androstenedione; Congenital Abnormalities; Female; Humans; Hydroxyprogesterones; Maternal Age; Ovarian Diseases; Ovary; Pedigree; Testosterone; Turner Syndrome

1974