Page last updated: 2024-10-16

adenine and Familial Turner Syndrome

adenine has been researched along with Familial Turner Syndrome in 1 studies

Research Excerpts

ExcerptRelevanceReference
"Noonan syndrome is a well-known clinical entity comprising multiple congenital anomalies characterized by typical facial features, short stature and congenital heart defect."1.32Genetics and variation in phenotype in Noonan syndrome. ( Jongmans, M; Noordam, K; Otten, B; van der Burgt, I, 2004)

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Jongmans, M1
Otten, B1
Noordam, K1
van der Burgt, I1

Other Studies

1 other study available for adenine and Familial Turner Syndrome

ArticleYear
Genetics and variation in phenotype in Noonan syndrome.
    Hormone research, 2004, Volume: 62 Suppl 3

    Topics: Adenine; Adult; Child; Cytosine; Exons; Female; Genetic Variation; Genotype; Guanine; Humans; Infant

2004